Impact Factor 5.753 | CiteScore 8.2
More on impact ›

ORIGINAL RESEARCH article

Front. Plant Sci., 28 May 2021 | https://doi.org/10.3389/fpls.2021.639253

A Machine Learning Approach to Prioritizing Functionally Active F-box Members in Arabidopsis thaliana

  • 1Department of Environmental and Plant Biology, Ohio University, Athens, OH, United States
  • 2Interdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, OH, United States

Protein degradation through the Ubiquitin (Ub)-26S Proteasome System (UPS) is a major gene expression regulatory pathway in plants. In this pathway, the 76-amino acid Ub proteins are covalently linked onto a large array of UPS substrates with the help of three enzymes (E1 activating, E2 conjugating, and E3 ligating enzymes) and direct them for turnover in the 26S proteasome complex. The S-phase Kinase-associated Protein 1 (Skp1), CUL1, F-box (FBX) protein (SCF) complexes have been identified as the largest E3 ligase group in plants due to the dramatic number expansion of the FBX genes in plant genomes. Since it is the FBX proteins that recognize and determine the specificity of SCF substrates, much effort has been done to characterize their genomic, physiological, and biochemical roles in the past two decades of functional genomic studies. However, the sheer size and high sequence diversity of the FBX gene family demands new approaches to uncover unknown functions. In this work, we first identified 82 known FBX members that have been functionally characterized up to date in Arabidopsis thaliana. Through comparing the genomic structure, evolutionary selection, expression patterns, domain compositions, and functional activities between known and unknown FBX gene members, we developed a neural network machine learning approach to predict whether an unknown FBX member is likely functionally active in Arabidopsis, thereby facilitating its future functional characterization.

Introduction

Since the first group of land plants emerged on the earth, various harsh conditions such as drought, severe temperatures, soil salinity, pathogen and insect infections, and herbivore attacks have become inevitable living conditions. The climate changes and humanmade environmental damages have been adding more challenges to plant growth and survival. To cope with an ever-changing living environment, the sessile lifestyle requires plants to carry out rapid adjustment of internal metabolic pathways to percept, transduce, and respond to numerous internal and external cues. Since the first genome of Arabidopsis thaliana (Arabidopsis hereafter) was obtained in 2000 (Arabidopsis Genome Initiative, 2000), numerous genome sequencing projects have exclusively demonstrated one robust metabolic regulatory machinery that is composed of a large group of members in plant genomes. This machinery is called the Ubiquitin (Ub)-26S Proteasome System (UPS).

The UPS is designed to regulate protein functions post-translationally. The entire system can be spatially and temporarily divided into two tandem biochemical pathways, ubiquitylation and degradation. Ubiquitylation of protein substrates usually takes place by a three-step cascade biochemical reaction that involves one common Ub-activating (E1) enzyme, few Ub-conjugating (E2) enzymes, and a large group of Ub ligases (E3) (Hershko and Ciechanover, 1998; Vierstra, 2009; Hua and Vierstra, 2011; Finley et al., 2012; Marshall and Vierstra, 2019). In general, it is the E3 ligases that determine whether a ubiquitylation substrate is routed into the UPS regulation. Protein ubiquitylation results in the changes of activity and/or intracellular locations of a substrate, but in many cases, leads a substrate to turn over. If a ubiquitylation substrate is tagged by poly-Ub chains, in which the Ub moieties are connected through their 11th or 48th lysine (K11/K48) residues, it will be recognized by the 26S proteasome for degradation (Kim et al., 2013; Yau and Rape, 2016; Marshall and Vierstra, 2019). Although emerging data suggested that the 26S proteasome and Ub-conjugating enzymes could change the fate of a ubiquitylation substrate (Kataria et al., 2014; Marshall and Vierstra, 2019), the biochemical functions of E3 ligases have been well appreciated for their specific roles in recruiting protein substrates into the UPS regulatory pathway (Vierstra, 2009; Hua and Yu, 2019). It has been estimated that an equally large group of E3 ligases and ubiquitylation substrates are encoded in plant genomes.

However, due to the challenge in identifying many short-lived and low abundant ubiquitylation substrates, the essential regulatory roles of the plant UPS were initially recognized by the large group of E3 ligases encoded in plant genomes. Because many E3 ligases are composed of protein families that share common protein-protein interaction domains, identifying E3 ligases is relatively easier than characterizing ubiquitylation substrates. For example, right after the first draft of Arabidopsis genome was sequenced in 2000 (Arabidopsis Genome Initiative, 2000), 695 F-box (FBX) genes were identified in this plant (Gagne et al., 2002). Since then, the completion of more plant genome sequencing projects has revealed that the UPS, particularly the E3 ligase group, has dramatically expanded in land plants compared to any other eukaryotic organisms. It has been suggested that the large expansion of the UPS is important for plants to cope with environmental changes (Grau-Bove et al., 2015).

The FBX genes encode a protein that contains at least two distinct protein-protein interaction modules, an N-terminal FBX domain (FBXD) and a C-terminal substrate recognition module. Through interacting with the S-phase Kinase-associated Protein 1 (Skp1) via the FBXD, all the functionally active FBX proteins assemble a Skp1-CUL1-FBX (SCF) multi-subunit E3 ligase complex. In this complex, CUL1 plays a scaffold role to dock the heterodimeric Skp1-FBX proteins at its N-terminus and a Really Interesting New Gene Box 1 (RBX1) at its C-terminus. During the ubiquitylation process, a Ub-conjugating enzyme associates with RBX1 in the complex to bring an activated Ub in close proximity to the SCF substrate that is recruited through interacting with the C-terminal substrate recognition module of the FBX protein (Zheng et al., 2002). Such a structural design results in the formation of an isopeptide bond between the carboxyl group of the C-terminal glycine residue of the Ub and the ε-amino group of a lysine residue on the substrate. Due to the presence of seven lysine residues on Ub, multiple Ubs can be conjugated sequentially with a preceding Ub moiety to form a poly-Ub chain. Although it is yet unknown whether SCF E3 ligases catalyze a specific type of ubiquitylation reaction, various structural topologies of poly-Ub chains can occur if the Ub moieties are conjugated through different lysine residues (Welchman et al., 2005; Yau and Rape, 2016). Hence, the resulting ubiquitylated substrates can have different fates either changing functions or being recognized by the 26S proteasome for degradation. Through the past two decades of functional genomic studies in Arabidopsis, a handful of FBX genes have been either phenotypically or biochemically characterized. To date, all the known SCF substrates in Arabidopsis are ultimately turned over by the 26S proteasome, suggesting that the plant-type SCF complexes primarily mediate the polyubiquitylation of their substrates via K48 or K11 on the Ub moieties. Through these studies, SCF complex-mediated ubiquitylation has been demonstrated to regulate a wide range of developmental processes, from early seed germination (Ariizumi et al., 2011; Majee et al., 2018), photomorphogenesis (Quint et al., 2005; Moon et al., 2007; Gilkerson et al., 2009; Yapa et al., 2020), circadian rhythms (see review by Johansson and Staiger, 2015), cell cycle (del Pozo et al., 2006; Kim et al., 2008; Noir et al., 2015) to late floral organ establishment (Zhao et al., 1999; Durfee et al., 2003; Yapa et al., 2020), self-incompatibility (Hua et al., 2008; Li and Chetelat, 2015; Sun et al., 2018), and embryogenesis/seed development (Liu et al., 2004; Yapa et al., 2020). In addition, SCF complexes are also known to play important roles in stress responses (Cheng et al., 2011; Hedtmann et al., 2017; Doroodian and Hua, 2021) and hormone signaling (see reviews by Santner and Estelle, 2010; Hua and Vierstra, 2011). Recently, we discovered a new role of SCFCFK1 complex in epigenetic regulation by controlling the stability of de novo DNA methyltransferase (Chen et al., 2020).

Given the large size of the Arabidopsis FBX gene superfamily, the number of characterized members is significantly lower than those in many other angiosperm core gene families (Li et al., 2016). To tackle this puzzle, several research groups have been studying the genomic and evolutionary features of this unique gene family. Through phylogenetic studies, Gagne et al. (2002) first discovered that the Arabidopsis FBX genes can be phylogenetically separated into 20 distinct groups with various sizes. Given the diverse FBXD sequences, Gagne et al. (2002) hypothesized that different groups of FBX proteins may preferentially bind to different Arabidopsis Skp1 like (ASK) proteins. However, direct biochemical and in vivo functional evidence that may support this hypothesis is yet lacking. The increasing number of sequenced plant genomes make it possible to carry out comparative genomic studies of the plant FBX gene family. Through size comparison among Arabidopsis, rice, and Populus, Yang et al. (2008) concluded that herbaceous annual plants encoded more FBX genes than woody perennial plants, arguing that the fewer FBX genes in Populus are integral to its biological processes. However, through further careful comparison across 18 plant genomes, ranging from the green alga Chlamydomonas reinhardtii to numerous monocots and eudicots, we disagreed with this conclusion. Instead, the results of our studies are in favor of a genomic drift evolutionary theory, by which the plant FBX gene family could expand in a process that is not related to the complexity of a plant species. For example, Zea mays and Sorghum bicolor are two closely related monocotyle species that split 12 million years ago (mya). However, S. bicolor encodes a greater than twofold of the number of FBX genes predicted in Z. mays (Hua et al., 2011). Subsequent studies in 443 Arabidopsis populations allowed us to discover that the expression of a large group of Arabidopsis FBX genes is epigenetically suppressed and their coding sequences are undergoing a rapid process of pseudogenization (Hua et al., 2013). Xu et al. (2009) discovered that unusually frequent shifts of exon-intron boundaries and/or frameshift mutations resulted in the size variance of the FBX gene families in Arabidopsis, poplar, and rice. Without further expression and functional studies, the adaptive role of FBX sequence divergence in plants is hypothetic. Recently, through genomic comparison of a large number of plant genomes (in total, 111 species), we discovered four clusters of plant FBX genes that experienced different retention rates, functional constraints, and phylogenetic distributions. This discovery allowed us to develop purifying and dosage balancing selection models for the evolution of plant FBX genes. Because lineage/species-specific FBX genes are detrimental due to the activation of unwanted degradation of numerous substrates, these members are kept in low frequencies in plant genomes, a phenomenon similar to the frequency suppression of detrimental alleles by purifying selection in populations. Therefore, in analogy to the purifying selection on detrimental alleles, we adapted the term purifying selection to explain the frequency suppression of FBX genes across plant genomes. However, like genetic drift of deleterious alleles in populations, these putatively harmful FBX members could have largely expanded in few plant genomes if their activities are suppressed such as epigenetic suppression in Arabidopsis (Hua, 2021).

Our new purifying selection model of the plant FBX genes raised a new challenge in their functional genomic studies in plant genomes. Although many drifted members remain inactive, some, like drifted alleles, could restore their activities and thus play a role in plant adaptation. For example, out of 111 green plant genomes, Kink Suppressed in BZR1-1D (KIB) 1/2 and EIN2 Targeting Protein (ETP) 1/2 are two pairs of recently duplicated FBX genes that are only identified in 5 and 8 Brassicaceae species, respectively (Hua, 2021). However, they have been shown to promote degradation of Brassinosteroid (BR)-Insensitive 2 (BIN2) and EIN2, in BR and ethylene signaling pathways, respectively, in Arabidopsis (Qiao et al., 2009; Zhu et al., 2017). To effectively tackle the yet-unidentified pathways involving plant FBX genes, new approaches have to be utilized. In this work, we presented a machine learning approach to prioritizing the functionally active FBX members in Arabidopsis for our future functional genomic studies. This approach is based on analyses of multiple dimensional features of known FBX genes, with these attributes used to identify unknown candidates that likely play an active role in regulating plant growth and development. Such an approach is rare but striking in the field. We believe it could be also adapted into the functional genomic studies of many other UPS families, several of which are also composed of a large group of members.

Materials and Methods

Data Acquisition

The list of Arabidopsis FBX genes was selected based on two studies in Hua et al. (2011) and Hua (2021). Only the FBX genes predicted in both studies as well as annotated in Araport11 available at The Arabidopsis Information Resource (TAIR)1 were selected for further study. Based on the accession number, 11 characteristics of each FBX gene were collected from TAIR. These characteristics included (1) number of publications, (2) number of expression sequence tags (ESTs), (3) clones of complementary DNA (cDNAs), (4,5) number of introns and exons, (6) total number of transfer DNA (T-DNA) insertions in the genomic region of the FBX gene from 100 bp upstream of the transcription start site to the stop codon, and (7–11) the number of T-DNA insertions in five different regions of the FBX locus, which were defined as the 100 bp upstream of the transcription start site, the front and rear halves of the coding region, and the front and rear halves of the non-coding region.

The ratio of the number of non-synonymous substitutions per non-synonymous site (Ka) to the number of synonymous substitutions per synonymous site (Ks), Ks value, and neutral evolution feature of each FBX gene were retrieved from Hua et al. (2011). The protein-protein interaction domain information of each encoded FBX protein was obtained from Hua (2021). The subdomain families of each parental domain were combined and counted as the same group. The RNA-Seq expression data of each FBX gene was retrieved in batch at http://ipf.sustc.edu.cn/pub/athrna/ (Zhang et al., 2020).

Multi-Dimensional Clustering Analysis

The resulting multi-characteristic data frame was subject to a k-means clustering analysis. The R package “ConsensusClusterPlus” was utilized to better determine the cluster number and clustering confidence, using the following settings: maxK = 9, reps = 1,000, pItem = 0.8, pFeature = 1, innerLinkage = “average,” finalLinkage = “average,” clusterAlg = “km,” distance = “Euclidean” (Monti et al., 2003; Wilkerson and Hayes, 2010).

Sequence Alignment and Phylogenetic Analysis

The predicted FBXD sequences retrieved from each set of FBX proteins were compared and aligned with both MUSCLE (Edgar, 2004) and MAFFT (Katoh et al., 2019). The consensus alignment was resolved by trimming ambiguously aligned sites in both alignments using Trimal (-conthreshold 0.5) (Capella-Gutierrez et al., 2009). The resulting sequence alignment was used to conduct a maximum likelihood phylogenetic analysis in RAxML with a PROTGAMMAJTT substitution model (Stamatakis, 2014). The statistical significance was evaluated with 1,000 bootstrap replicates using a rapid bootstrap analysis.

Supervised Machine Learning

Three machine learning approaches, including Artificial Neural Network (ANN) (Khan et al., 2001), Random Forest (RF) (Breiman, 1996, 2001; Diaz-Uriarte and Alvarez de Andres, 2006), and Support Vector Machine (SVM) (Vanitha et al., 2015), were adopted from the R packages, “neuralnet” (Fritsch et al., 2019), “randomForest” (Liaw and Wiener, 2002), and “e1071” (Meyer et al., 2020), respectively. After multiple runs, the settings for developing each machine learning model were optimized as follows: (1) we used two hidden layers with 10 and 2 nodes for ANN modeling; (2) a default setting except for “mtry = 4” was used in RF analysis; (3) for SVM learning models, we used the following settings: type = “C-classification”; kernel = “radial.”

All the machine learning predictions were performed on the same input dataset for 10 rounds with each round undergoing 1,000 times of resampling. In each resampling analysis, three different sets of samples, including training, validating, and testing samples, were selected from a total of 692 FBX genes with different levels of functional understanding up to date. From a pool of 41 well-studied and 123 out of 140 poorly studied FBX genes (1:3 ratio), we randomly selected 109 and 55 of them (2:1 ratio) as training and validating samples, respectively (Supplementary Script 1). The validating sample was used to examine prediction accuracy for well and poorly studied FBX genes based on the prediction model developed using the training sample. The testing sample contains the remaining 470 functionally unknown FBX genes that were examined and a second set of 41 known FBX genes serving as internal positive controls. The functionally active and inactive FBX genes predicted in 950 out of 1,000 times of resampling analysis were separately combined into two final prediction datasets. If an FBX gene was identified in 9 or greater from 10 rounds of predictions, it was considered a good candidate in each of the two final prediction datasets.

Statistical Analysis by R

The statistical analyses were performed using in-house R scripts as described in Supplementary Scripts 1, 2 based on the processed data in Supplementary Data 13.

Results

Categorizing Arabidopsis FBX Genes

Based on our previous phylogenetic studies of FBX genes in 18 plant genomes (Hua et al., 2011), we retrieved the Arabidopsis members and searched the literature record of their functional studies at TAIR (see text footnote 1). Since our discovery on the genomic drift evolution of the FBX gene superfamily in plants (Hua et al., 2011), much effort has been made in the field to better understand the genomic and biochemical features of FBX proteins, which, in part, is evidenced by the update of five different subgroups of FBX Pfam-HMM profiles, including F-box, F-box-like, F-box-like_2, F-box_4, and F-box_5 (Pfam 32)2. To better predict the plant FBX genes in each genome, we recently developed a plant specific FBX HMM profile, named AO_FBX.hmm, based on 1,341 non-redundant FBXD sequences predicted in Arabidopsis and rice (Hua et al., 2011; Hua, 2021). Using these six FBX HMM profiles, we applied a Closing Target Trimming (CTT) high throughput superfamily annotation method and predicted in total 78,471 FBX genes in 111 plant species (Hua and Early, 2019; Hua, 2021). According to this new prediction, 14 previously predicted Arabidopsis FBX genes were not further analyzed in this work. In total, 696 FBX genes were selected for further analysis (Supplementary Data 1).

Through careful literature studies, we hypothesized that the functionality of an FBX gene is correlated with its number of publications because a functionally active gene is relatively easy to be identified and could be involved in multitude pathways that result in more publications. For example, Transport Inhibitor Response 1 (TIR1) and COronatine Insensitive 1 (COI1) are two FBX members that have more than 100 publications, which are consistent with their important roles as the receptors for auxin and jasmonic acid, respectively (Xie et al., 1998; Dharmasiri et al., 2005; Tan et al., 2007; Sheard et al., 2010). Hence, we categorized the total of 696 Arabidopsis FBX genes into four groups based on how well they have been studied up to date (Supplementary Data 1). If an FBX gene is well studied with its substrate also characterized, we considered it as a Group I member. In total 41 Group I FBX genes were identified (Supplementary Table 1). Importantly, the protein products of all Group I FBX genes have been demonstrated to interact with ASK1 protein (Supplementary Table 1), suggesting that ASK1 is a predominant Skp1 member in Arabidopsis as has been discovered in our previous studies (Hua and Gao, 2019; Yapa et al., 2020). There are also 41 FBX genes that have been phenotypically characterized with observable mutant phenotypes but without known substrates. We assigned them into Group II (Supplementary Data 1). Next generation sequencing technology has benefited a number of transcriptomic studies. If the expression of an FBX gene significantly responds to specific physiological and/or developmental processes, it could have been identified in these studies although its mutant phenotype and molecular mechanism are unknown. In total, 472 members have been reported to be significantly differentially expressed in 121 transcriptome-wide studies (retrieved from TAIR, see text footnote 1). We defined them as Group III FBX genes. The remaining 142 FBX genes that have never been reported in any work described above were combined as Group IV members. Not surprisingly, the number of publications varied significantly among these four groups (Figure 1A; p = 0.04 for Group I and Group II comparison and p = 0 for all the other pairwise comparisons, Kruskal-Wallis rank sum test followed by Dunn’s test with Benjamini-Hochberg multiple testing correction). While Group I FBX genes have 27 ± 50 (mean ± SD, hereafter the same) publications per member, each of the remaining FBX genes has 5.8 ± 3.8, 2.2 ± 1.9, and 0 publications in Groups II, III, and IV, respectively (Figure 1A).

FIGURE 1
www.frontiersin.org

Figure 1. Categorizing four groups of Arabidopsis FBX genes. (A) Comparison of number of publications related to each FBX gene. (B) Differential frequencies of CTDs in each group of FBX proteins resulted in rich and rare groups of CTDs. The number in each grid shows the proportion of CTD-containing FBX proteins in each indicated group or the entire FBX family.

Sequence Comparison Between Known and Unknown FBX Genes

The specificity of an FBX protein is primarily determined by its C-terminal substrate recognition module (Zheng et al., 2002; Hua and Vierstra, 2011). To examine whether the differential functionalities of FBX genes are attributed to the C-terminal sequence variance of their encoded proteins, we annotated all known protein-protein interaction domains by searching the FBX protein sequences against the Pfam-A database (Pfam 32; see text footnote 2), which contained the HMM profiles for 17,933 protein-protein interaction domains (families). In total, 238 different domains were identified as putative C-terminal substrate binding domains (CTDs) (Supplementary Data 2).

By combining the top 10 abundant CTDs from each of the four groups and the entire set of FBX proteins (All), we identified in total 24 CTDs that are differentially represented. We clustered the CTDs according to their frequencies in each group. Interestingly, two distinct clusters of CTDs are resolved. While Leucine Rich Repeats (LRR), Kelch, FBX associated (FBA), and FBX binding (FBD) domains are clustered in a group that represents 70% of the total Arabidopsis FBX proteins, the remaining 20 CTDs are present in fewer FBX proteins except for Arm, which is only found in Group II (Figure 1B).

Among the four different groups of FBX proteins compared, Group I is significantly enriched with Kelch domains (Fisher’s exact test, p = 6.2e-4, 2.9e-2, and 6.3e-6 in comparison with Groups II, III, and IV, respectively). TIR1 protein domain (Transp-inhibit) and Arm domains are exclusively present in Groups I and II FBX proteins, respectively (Figure 1B). FBA and FBD seem to be enriched in the protein sequences encoded by FBX genes that are not well studied. They have the highest frequencies in Group IV followed by Group III FBX members. Some rare CTDs are also unique to Group III or IV groups. For example, Toxin, Y1, Toprim, TLP-20, SpoIIP, and DUF3794 are only found in Group IV FBX proteins and Sel1 and TetR are unique to Group III FBX proteins. It is yet unknown whether some of these rare CTDs resulted from the rapid sequence divergence process of recently duplicated FBX genes. It is known that recently duplicated FBX genes have high rates of non-synonymous mutations and frequent shifts of exon-intron boundaries (Xu et al., 2009; Hua et al., 2011). Such high rates of mutations may generate rare CTDs de novo. To support this hypothesis, we searched these rare CTDs in the entire predicted Arabidopsis proteome (in total 27,654 proteins). Among 30 protein sequences found to possess one of these CTDs, 13 also contain an FBXD, indicating an overrepresentation of FBX proteins in these rare CTD-containing proteins compared to the entire proteome (43% vs. 2.3%, Fisher’s exact test, p = 1.5e-13).

Phylogenetic Comparison of Four Groups of F-box Genes

Recently duplicated FBX genes are likely phylogenetically clustered together to form separate groups from ancient duplicates. Since ancient members may be under strong functional constrains for their long period of retention in the genome, we speculated that Groups I and II FBX genes may be clustered differently with the other two groups. To test this hypothesis, we retrieved the FBXD sequence of each FBX protein and carried out a maximum likelihood phylogenetic analysis. Although the majority of bootstrap values are too low to be statistically significant, the phylogenetic tree of 696 FBXD sequences can be approximately divided into FBA, Kelch, unknown, and LRR four large groups along with several small subfamilies, such as TIR1-containing Transp-Inhibit, TUB, WD40, DUF295, and FBD subfamilies, some of which (e.g., Transp-Inhibit, TUB, DUF295) are in general supported with a high bootstrap value (Figure 2A and Supplementary Figure 1). Therefore, the FBXD sequences were clustered in groups consistent with the CTD feature of an FBX protein, further suggesting a coevolutionary process between the FBXD and the CTD in an FBX protein sequence (Figure 2B; Gagne et al., 2002). However, surprisingly, the FBXD sequences encoded by Groups I and II genes are not completely clustered into isolated clades from those of Groups III and IV FBX genes. Although they are enriched in LRR, Kelch, and Arm domain encoding FBX genes, some also code a CTD that contains FBA and other unknown or rare domains (Figures 1B, 2B and Supplementary Figure 1), making the phylogenetic analysis difficult for predicting FBX members that are functionally active.

FIGURE 2
www.frontiersin.org

Figure 2. Phylogenetic distribution of four groups of Arabidopsis FBX genes. (A) Number comparison of FBX proteins containing top 10 CTDs in three different studies indicates slight prediction changes. The number shown in the parenthesis indicates the number of FBX proteins identified in this study. (B) A maximum likelihood phylogenetic analysis of 696 FBX genes based on their encoded FBXD sequences. The most abundant CTD in each FBX protein was identified and color coded as in (A) in the branches toward the node where it resides. The tree was generated using RAxML with a PROTGAMMAJTT substitution model. The known names of Groups I and II FBX proteins were labeled and highlighted with red and blue colors, respectively. Scale bar: amino acid changes per site. An expanded version with statistically significant bootstrap values can be found in Supplementary Figure 1.

An Unsupervised Clustering Approach to Finding Active FBX Genes

The wide distribution of known FBX genes in the phylogenetic tree found in this study and our recent finding about the purifying and dosage balancing selections on the FBX gene duplication process suggest two important evolutionary characteristics of Arabidopsis FBX genes. First, a significant number of FBX genes are functionally inactive and remain lineage/species-specific due to purifying/negative selection that prevents them from expanding across genomes. Second, functionally active FBX genes could arise from the lineage/species-specific group, such as KIB 1/2 and ETP1/2 in the DUF295 and FBA groups, respectively (Figure 2B and Supplementary Figure 1). To effectively guide future functional genomic studies of the Arabidopsis FBX genes, we hypothesized that the functionally active FBX members share some common genomic, sequence, and transcriptomic features that may allow us to predict their relationship. Hence, we developed a multiple dimensional dataset that includes 27 characteristics of 692 Arabidopsis FBX genes (Supplementary Data 3). Four FBX genes, AT1G24800 and AT1G25055 from Group III and AT5G36730 and AT5G36820 from Group IV, were removed for further studies due to their lack of any data in a large collection of RNA-Seq expression dataset with 20,068 samples (Zhang et al., 2020).

Based on this large data collection, we utilized a resampling-based unbiased k-means clustering method (Monti et al., 2003; Wilkerson and Hayes, 2010) to search for a potential list of genomic features that may be correlated with the functional activities of FBX genes. First, we analyzed the entire dataset to identify four k-means clusters (Figure 3A). Cluster 1 is significantly more enriched with Groups I and II FBX genes than with those from the other two groups. Cluster 3 seems to contain a similar proportion of FBX members from Groups II, III, and IV whereas the remaining two clusters (2 and 4) are enriched with Groups III and IV FBX genes. The differential clustering result of the four groups of FBX genes confirms the presence of distinct genomic and functional features among FBX genes. To further examine how well the four clusters of FBX genes were separated, we performed principal component analysis (PCA). Unfortunately, PC1 and PC2 only explained a mild proportion of the variance across 692 FBX genes which resulted in a large fraction of FBX genes that were overlapped among Clusters 2, 3, and 4 (Figure 3B). Hence, some vectors (characteristics) in the dataset disrupted the classification of FBX genes.

FIGURE 3
www.frontiersin.org

Figure 3. Unsupervised k-means clustering demonstrates distinct and overlapping features of four predefined groups of FBX genes. (A) Fraction distribution of four predefined groups of FBX genes as in Figure 1A in four k-means clusters classified based on 27 FBX characteristics shown in Supplementary Data 3. (B) A biplot showing the first two dimensions of a principle component analysis (PCA) of four groups of FBX genes. PC1 and 2 indicates the percentage of variance between individuals. Colored data points indicate the four clusters obtained from the analysis in (A) and the numbers indicate the four predefined groups of FBX genes. (C) Fraction distribution of four predefined groups of FBX genes in three k-means clusters as analyzed in (A) except for using 10 out of 27 FBX characteristics available in Supplementary Data 3. (D) Multivariate biplot of PCA analysis of four groups of FBX genes based on the same data set as in (C). The contribution of the first two PCs explained 54.7% of the total variation. Data points are color coded and labeled as in (B). Each arrow indicates the direction of the largest effect of the corresponding variable (characteristics) and the length of the arrow shows its influential strength. The angle between one pair of arrows reflects their correlations in the data set.

To better distinguish FBX genes with different functional activities, we performed multiple k-means clustering by selecting different number of vector combinations from the same dataset. We found three k-means clusters calculated based on 10 selected characteristics to better separate the four groups of FBX genes identified above (Figures 1, 3C,D). While Cluster 1 enriched Groups I and II FBX genes, the large fractions of Groups III and IV FBX genes were present in Cluster 3. Cluster 2 contains a significant proportion of Groups I, II, and III FBX genes. The PCA result demonstrated that 43.0 and 11.7% of the variance among the FBX genes could be explained by PC1 and PC2, respectively (Figure 3D). Among 10 vectors, mean and median expression, the number of complementary DNAs (cDNAs) and expression sequence tags, number of publications, and Ks values are positively correlated with the functional activities of FBX genes (i.e., more Groups I and II members). Conversely, the higher the expression coefficient variation (CV) and the Ka/Ks value, the less active the FBX gene is (i.e., more Groups III and IV members). The maximum expression value and the number of introns seem not so distinguishable as the other vectors among FBX genes with different functional activities (Supplementary Data 3). Our previous study has discovered that the highest expression of many FBX genes could result from epigenomic programming regulation but not necessarily be related to its functional activity (Hua et al., 2013). The lack of correlation between the maximum expression value and the functional activity of an FBX gene further confirmed this notion.

Ranking the Top Candidates of Unidentified Functionally Active FBX Genes by Neural Network Machine Learning

Clustering analysis found a significant number of Groups I and II FBX genes that were clustered together with the other two groups. For example, 15, 29, 47, and 46% of Groups I, II, III, and IV FBX genes, respectively, were clustered in Cluster 3 if we evaluated all 27 vectors (Figure 3A). When we used a better clustering data matrix, 44, 49, and 26% of Groups I, II, and III FBX genes, respectively, were found in Cluster 2. More intriguingly, only 9% of Group IV FBX genes were present in this cluster, suggesting that some Group III FBX genes could be also functionally active. Given that 41 Group I FBX genes are much better studied than any other group members and that 140 Group IV members have never been studied up to date (Figure 1A), we assigned them as functionally active and inactive members, respectively. Based on this prior condition, we sought to use a supervised machine learning approach to rank the functional activities of 470 Group III FBX genes whose functions are yet unknown.

Artificial neural network (ANN) is a machine learning algorithm that simulates the structure and behavior of human brain neurons (Khan et al., 2001). ANN applies a binary classification model to train and categorize complex patterns that are hidden in a large dataset. It operates an interconnected set of nodes with three kinds of layers, including input, hidden, and output layers, to make stepwise decisions (Greer and Khan, 2004). Since the data structure can change when external or internal data information flows through the network, it is suitable for analyzing non-linear interactions between dependent and independent variables (Pirooznia et al., 2008). Taking advantage of ANN decision analysis, we developed a novel bioinformatic pipeline to rank the activities of Arabidopsis FBX genes.

As described above, we treated Groups I and IV FBX genes as being functionally active and inactive, i.e., 1 and 0 for ANN analysis, respectively (Figure 1A, Supplementary Data 1, and Supplementary Script 1). In total, 41 Group I and 123 out of 140 Group IV (1:3 ratio) FBX genes were combined and randomly sampled into two datasets containing 109 and 55 FBX genes (2:1 ratio), which were used as training and validating samples, respectively (Supplementary Script 1). The validating sample was used to examine prediction accuracy and false discovery rate. The test sample includes 41 and 470 FBX genes from Groups II and III, respectively. Since Group II FBX genes have been phenotypically characterized with known mutant phenotypes, we further used this group of FBX genes as internal controls for examining the efficiency of our prediction. To increase the prediction confidence, we selected the consistent predictions from 9 or greater of 10 rounds of ANN analyses as our final result. In addition, we ran 1,000 times of resampling for each round of ANN analysis and only if an FBX gene was predicted in 950 out of 1,000 times of resampling would we consider it as a functionally active or inactive candidate in that round of analysis.

Given the differential k-means clustering results from two datasets that contain 27 and 10 characteristics of the FBX genes (Figure 3), we also examined their influences on the ANN performance, which were designated as Methods 1 and 2, respectively. Interestingly, we observed an overall better prediction in Method 2 compared to Method 1. For example, on average, 96% of the validating samples (53 out of 55 FBX genes) were accurately predicted in Method 2 whereas Method 1 yielded 90.2% accuracy on this prediction (Figure 4A). Consequently, Method 1 resulted in 8.8 and 5.0% more false negative and false positive predictions, respectively, than Method 2 (Figure 4B). The high false prediction rate gave Method 1 to predict slightly more active FBX genes than Method 2 (Figure 4C). However, the goal of our machine learning is to find the best but not the highest number of candidates that could facilitate the finding of new FBX gene functions. Hence, similar to the unsupervised k-means clustering analysis, the shortened list of genomic and transcriptomic characteristics may better predict functionally active FBX genes. Consistently, compared to the k-means clustering result of the same dataset (10 characteristics, Figures 3C,D), the predicted functionally active FBX genes candidates are present in Clusters 1 and 2, while 90.2% of predicted functionally inactive FBX genes candidates are present in Cluster 3 (Figure 4D). Not surprisingly, Group II FBX genes (internal positive controls) were predicted to be significantly more enriched in the functionally active group than in the inactive group (28% vs. 1.6%, p = 2.4e-09, Fisher’s exact test; Supplementary Data 4).

FIGURE 4
www.frontiersin.org

Figure 4. Performance evaluation of ANN prediction for functionally active and inactive FBX genes. (A) Prediction accuracy based on predefined Group I (active) and Group IV (inactive) validating FBX genes. Methods 1 and 2 utilized the dataset containing 27 and 10 variables, respectively, from Supplementary Data 3 as described in Figure 3. (B) False predication rates based on predefined Group I (active) and Group IV (inactive) testing FBX genes. Methods 1 and 2 are as in (A). (C) Fractions of predicted active FBX genes in Groups II and III. Methods 1 and 2 are as in (A). (D) Distribution of predicted active FBX genes in three k-means clusters obtained in Figures 3A–D. The number of p-values shown in (A–C) were calculated based on Welch two sample t-test.

Verification of Unknown Active FBX Genes by Alternative Machine Learning Approaches

The prediction of functionally active and inactive FBX genes by ANN analysis is encouraging. Although both the validating sample (containing Group I and IV FBX genes that serve as active and inactive controls) and the internal controls (Group II) suggest that ANN has a good performance (Figure 4), we further developed multiple lines of evidence, including bioinformatic, phylogenetic, expression, and evolutionary comparisons, to confirm the prediction precision.

In addition to ANN machine learning, several additional approaches are also available for this objective (Pirooznia et al., 2008). For example, Random Forest (RF) utilizes classification trees for clustering variables through bootstrap aggregation and random selection for tree construction (Breiman, 1996, 2001; Diaz-Uriarte and Alvarez de Andres, 2006). Support Vector Machine (SVM) is another approach for variable clustering based on structural risk minimization (SRM) theory (Vanitha et al., 2015). Both RF and SVM have been widely applied for decision making upon input of a large dataset. Therefore, we also utilized these two machine learning approaches to predict functionally active and inactive FBX candidates based on the same dataset used for Method 2 of ANN prediction.

The prediction accuracy from validating sample could be sensitive to the threshold applied in different algorithms. High prediction accuracy from the validating sample may sacrifice the prediction precision in test samples due to an unknown ratio of true and false members in the test samples. To better evaluate the performance of three machine learning approaches, we normalized the prediction accuracy from each validating sample by the total number of predicted functionally active and inactive FBX genes from the test sample. We defined this value as prediction precision. Interestingly, ANN outperformed both RF and SVM approaches (Figure 5A). More encouragingly, 44 and 53 out of 54 functionally active FBX genes predicted by ANN were also predicted by SVM and RF, respectively. However, the latter two methods yielded 1.7- and 3.9-fold more functionally active FBX genes than what ANN predicted (Figure 5B). Such a prediction is not very helpful for guiding future functional genomic studies. More FBX genes predicted can potentially weaken the priority of good candidates. In addition, ANN predicted a similar group of functionally inactive FBX genes as did RF although SVM predicted more members in this category (Figure 5C). Such variance can be neglected because the ultimate goal of this work is to guide the finding of new functions of functionally active FBX genes.

FIGURE 5
www.frontiersin.org

Figure 5. Performance comparison of ANN prediction with SVM and RF machine learning approaches. (A) Normalized prediction accuracy. The prediction accuracy calculated based on the same validating samples as described in Figure 4A was normalized by the total number of predicted active and inactive FBX genes. (B) A Venn diagram plotting showing the common and unique predictions of active FBX genes obtained from ANN with those obtained from SVM (left panel) and RF (right panel). (C) A Venn diagram plotting showing the common and unique predictions of inactive FBX genes obtained from ANN with those obtained from SVM (left panel) and RF (right panel).

Phylogenetic Verification of Unknown Active FBX Genes

The exclusive consistency in predicting the functionally active FBX genes among the three different machine learning approaches suggests that the predicted active and inactive FBX genes are significantly differentiated in their biological characteristics. Since ANN seemed to perform the best among the three approaches (Figure 5), we took the prediction of this approach (Method 2, Figure 4) for further verification. Because more inactive FBX genes were predicted (Figures 5B,C and Supplementary Data 4), we randomly sampled this dataset in order to keep the same number of active and inactive FBX genes for comparison. We examined how the predicted active and inactive members are phylogenetically related to the truly active FBX genes. Using the same approach as we constructed the phylogenetic tree of the entire FBX family (Figure 2B), we obtained a maximum likelihood tree that incorporates both predicted active and inactive members and Group I FBX genes. For better comparison, the tree has been rooted to EIN3-Binding F-box protein 1 (EBF1).

Surprisingly, we found that all the members were clustered with Group I FBX proteins in one single clade with strong statistical significance (Figure 6). Since all Group I FBX proteins are known to interact with ASK1, the monophyletic relationship of both unknown active and inactive FBX proteins with known active Group I FBX proteins further argues that many, if not all, Arabidopsis FBX proteins bind to ASK1. However, the distribution of predicted functionally active and inactive FBX proteins shows distinct phylogenetic patterns in relation to Group I FBX proteins. While predicted active FBX members intermingle with Group I FBX members in forming multiple mixed subclades, the predicted inactive members are in general clustered together (Figure 6). Hence, we concluded that the predicted functionally active FBX members are more phylogenetically related to Group I FBX genes than inactive ones.

FIGURE 6
www.frontiersin.org

Figure 6. Phylogenetic comparison of predicted active and inactive FBX genes with known Group I members. The phylogenetic tree was constructed as in Figure 2B except that the statistical significance equal to or greater than 50% of 1,000 times of bootstrap resampling is indicated in each corresponding node. The known names of Groups I and II FBX proteins were labeled and highlighted with red and blue colors, respectively. The identification names [described in Hua et al. (2011)] of predicted functionally active and inactive Group III FBX proteins were highlighted with magenta and black colors, respectively. Size bar: amino acid changes per site.

Distinct Genomic and Transcriptomic Features Between Active and Inactive FBX Genes

To further demonstrate our prediction precision biologically, we compared the predicted functionally active and inactive FBX members with Group I FBX genes at both expression variance and evolutionary constraint levels.

While no dramatic expression variance can be observed between Group I and the predicted functionally active FBX genes, both groups have extremely higher mean and median expression values than the predicted inactive FBX genes. Not surprisingly, the expression coefficient variance (CV) of predicted inactive FBX genes is significantly higher than the other two groups due to their extremely low mean expression values (Figures 7A–C; p = 0 for comparisons of Group I or predicted active FBX genes with inactive FBX genes, Kruskal-Wallis rank sum test followed by Dunn’s test with Benjamini-Hochberg multiple testing correction). Such dramatic expression variance between functionally active and inactive members suggests a good prediction precision of our dataset.

FIGURE 7
www.frontiersin.org

Figure 7. Verification of predicted active and inactive FBX genes according to their distinct expression and evolutionary features. The corresponding values of FBX genes were retrieved from Supplementary Data 3 and plotted against each other in the indicated groups. (A–C) Expression comparison of three indicated groups of FBX genes in 20,068 RNA-Seq samples (Zhang et al., 2020). (A) Mean expression per gene; (B) median expression per gene; (C) expression coefficient of variation (CV) per gene. (D,E) Distinction of evolutionary features among the indicated groups. (F) Comparison of predicted FBXD e-values among the indicated groups.

We further examined the difference of evolutionary constraints among these three groups. Functionally inactive genes are not always under strong evolutionary constraints and many could experience neutral changes, which result in high Ka/Ks ratios. When plotted with the Ka/Ks values of the FBX genes in three groups, the predicted group of functionally inactive FBX members showed an average of 0.62 ± 0.16 Ka/Ks value, significantly higher than 0.23 ± 0.11 and 0.30 ± 0.23, respectively, for the Ka/Ks values of the predicted functionally active FBX genes and Group I members. The Ka/Ks values of the latter two groups were not statistically significantly different (Figure 7D). Ks values could be used to indirectly indicate the age and types of a gene duplicate. The higher the Ks the more likely the gene duplicate resulted from an ancient whole genome duplication event, which is in general highly constrained (Li et al., 2016; Hua, 2021). Hence, we also compared the Ks differences among the three groups (Figure 7E). Surprisingly, we found that the predicted functionally active FBX genes had the highest Ks values followed by Group I FBX genes. This result further concluded the strong functional constraints of our predicted active FBX genes. The low Ks values of the predicted inactive FBX members are consistent with their weak functionality in Arabidopsis.

Previous genomic studies on the FBX genes often applied a Pfam search e-value to predict the presence of an FBXD in its encoded protein sequence. However, we have argued a potential drawback of this method in finding most, if not all, FBX genes in genomes in our previous studies through comparing our result with those from other research groups (Hua et al., 2011). For example, several well-studied Group I FBX proteins have high e-values. To provide an additional line of evidence, we evaluate the predicted FBXD e-values among the three groups. We found that the FBXD e-values of predicted functionally inactive FBX members were significantly lower than Group I (Figure 7F; p = 0.007; Kruskal-Wallis rank sum test followed by Dunn’s test with Benjamini-Hochberg multiple testing correction). Although we cannot rule out the possibility of physical interaction between an encoded inactive FBX protein with Skp1, the significantly higher e-values of Group I FBX proteins further suggested that the e-value cannot be used as an effective criterion for predicting a functionally active FBX gene in genomes (Hua et al., 2011).

Discussion

The plant FBX gene superfamily is arguably one of the largest, yet also largely unexplored, group of protein-coding genes. Although the past two decades of functional genomic studies in the model plant, Arabidopsis, have revealed a wide range of F-box protein functions, only 10% of the total ∼800 members have been genetically characterized (Supplementary Data 1; Hua et al., 2011, 2013; Hua, 2021). Making it even more challenging, the F-box proteins with known molecular mechanism and ubiquitylation substrates have been only about 5% of the family up to date (Supplementary Table 1). Not only the difficulties in proteomic identification of short-lived and low abundant FBX substrates but also the unique evolutionary processes made it extremely challenging to characterize the biological roles of FBX genes. In addition to our previous discovery showing the epigenomic suppression of a large set of Arabidopsis FBX genes (Hua et al., 2013), we recently proposed a novel evolutionary mechanism involving the FBX gene superfamily in 111 plant genomes (Hua, 2021). The study from this large group of plant species uncovered both purifying and dosage balancing selections that apply on different groups of plant FBX genes. While many inactive ones remain lineage/species-specific by strong purifying selection against their expansion in plant genomes, those active ones are under balancing selections whose copy numbers in a genome are determined by the pool of substrates. Such dual evolutionary processes may give rise to the unprecedented challenges in the functional genomic studies of the plant FBX genes.

Although evolutionary studies may help uncover a core group of plant FBX proteins, a significant proportion of the remaining lineage or even species-specific members could activate and restore an adaptive role for plant survival (Hua, 2021). Such members are hard to discover through evolutionary comparative studies. Fortunately, in part thanks to the advancement of next generation sequencing technologies, a tremendous amount of genomic and transcriptomic data has been accumulated up to date particularly in Arabidopsis. For example, we were only able to detect expression data for 330 Arabidopsis FBX gene in 4,933 microarrays available for Col-0 in the NASCArrays in 2013 (Hua et al., 2013). However, in this study, we found the expression data for 692 FBX genes in 20,068 RNA-Seq samples from Arabidopsis (Zhang et al., 2020), which significantly benefited us to decipher the expression variance of different groups of FBX genes.

Since some Group I FBX genes (well-studied) have a lower expression level than functionally inactive members, it would be challenging to identify them from functionally inactive members based on expression data (Figures 7A,B). To compare the relationship of FBX members with variant functionalities, one idea is to integrate their genomic, transcriptomic, sequence structure, and evolutionary features as many as possible. In this work, we collected 27 different types of FBX characteristics including number of publications, which served as indirect evidence of their activities (Supplementary Data 1, 3). Unsupervised k-means clustering was able to identify three or four separated clusters (Figure 3). However, due to significant overlaps among several clusters, such a clustering approach is not able to rank or prioritize the FBX gene members based on their functional activities. Fortunately, the development of multiple supervised machine learning algorithms in the science community allowed us to adapt them for our studies. The excellent prediction precision of ANN analysis is demonstrated by multiple lines of evidence in this study. First, it yielded ∼96% accuracy in predicting the predefined activities of a validating dataset (Figure 4A). Second, 98% of its predicted active FBX genes were also predicted by the other two machine learning approaches including SVM and RF, which were based on different algorithms (Figure 5B). Third, the FBX genes with known mutant phenotypes (Group II members in the test sample) were successfully predicted to be overrepresented in the functionally active group (Supplementary Data 4). Fourth, the predicted functionally active and inactive FBX genes demonstrated striking difference in phylogenetic relationship with known active FBX members (Figure 6). Fifth, both expression and evolutionary selection data further suggested that the predicted functionally active members were most likely active (Figure 7).

We believe that our approach in prioritizing the functionally active FBX members for future functional genomic studies is innovative. Such an approach can be routinely and iteratively applied to fine tune the best list of candidates based on what we know from the prior data. Although it seems that the more data the better, our study found that reducing some characteristics yielded a better classification of FBX genes in both k-means clustering and ANN machine learning (Figures 3, 4). Hence, irrelevant variables in the data matrix could impact the prediction accuracy by complicating calculation. Considering the enormous size of the plant UPS and its yet largely unknown substrates, developing machine learning approach-based artificial intelligent studies could effectively assist the discovery of new mechanisms in this system. However, the ultimate finding still relies on more effective and high throughput omics analyses in conjunction with individual fine-tuning work in both genetic and biochemical studies. The 50% of known FBX members lacking strong biochemical evidence (Group II) reflects the importance of developing this type of study in the field.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author Contributions

ZH conceived of the study, performed data analysis, wrote the manuscript, and gave final approval of the version to be published. YL drafted the machine learning approaches and assisted data analysis. YL and MMY assisted manuscript writing. All authors made substantial contributions to data acquisition, to interpretation and modification of the data, were involved in manuscript revisions, and read and approved the final manuscript.

Funding

The work was supported by a United States National Science Foundation CAREER award (MCB-1750361 to ZH).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2021.639253/full#supplementary-material

Footnotes

  1. ^ https://www.arabidopsis.org
  2. ^ https://pfam.xfam.org

References

Arabidopsis Genome Initiative (2000). Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408, 796–815. doi: 10.1038/35048692

PubMed Abstract | CrossRef Full Text | Google Scholar

Ariizumi, T., Lawrence, P. K., and Steber, C. M. (2011). The role of two f-box proteins, SLEEPY1 and SNEEZY, in Arabidopsis gibberellin signaling. Plant Physiol. 155, 765–775. doi: 10.1104/pp.110.166272

PubMed Abstract | CrossRef Full Text | Google Scholar

Breiman, L. (1996). Bagging predictors. Mach. Learn. 24, 123–140. doi: 10.1007/bf00058655

CrossRef Full Text | Google Scholar

Breiman, L. (2001). Random forests. Mach. Learn. 45, 5–32.

Google Scholar

Capella-Gutierrez, S., Silla-Martinez, J. M., and Gabaldon, T. (2009). trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics 25, 1972–1973. doi: 10.1093/bioinformatics/btp348

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, J., Jiang, J., Liu, J., Qian, S., Song, J., Kabara, R., et al. (2020). F-box protein CFK1 interacts with and degrades de novo DNA methyltransferase in Arabidopsis. New Phytol. 229, 3303–3317. doi: 10.1111/nph.17103

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheng, Y. T., Li, Y., Huang, S., Huang, Y., Dong, X., Zhang, Y., et al. (2011). Stability of plant immune-receptor resistance proteins is controlled by SKP1-CULLIN1-F-box (SCF)-mediated protein degradation. Proc. Natl. Acad. Sci. U.S.A. 108, 14694–14699. doi: 10.1073/pnas.1105685108

PubMed Abstract | CrossRef Full Text | Google Scholar

del Pozo, J. C., Diaz-Trivino, S., Cisneros, N., and Gutierrez, C. (2006). The balance between cell division and endoreplication depends on E2FC-DPB, transcription factors regulated by the ubiquitin-SCFSKP2A pathway in Arabidopsis. Plant Cell 18, 2224–2235. doi: 10.1105/tpc.105.039651

PubMed Abstract | CrossRef Full Text | Google Scholar

Dharmasiri, N., Dharmasiri, S., and Estelle, M. (2005). The F-box protein TIR1 is an auxin receptor. Nature 435, 441–445.

Google Scholar

Diaz-Uriarte, R., and Alvarez de Andres, S. (2006). Gene selection and classification of microarray data using random forest. BMC Bioinformatics 7:3. doi: 10.1186/1471-2105-7-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Doroodian, P., and Hua, Z. (2021). The ubiquitin switch in plant stress response. Plants (Basel) 10:246. doi: 10.3390/plants10020246

PubMed Abstract | CrossRef Full Text | Google Scholar

Durfee, T., Roe, J. L., Sessions, R. A., Inouye, C., Serikawa, K., Feldmann, K. A., et al. (2003). The F-box-containing protein UFO and AGAMOUS participate in antagonistic pathways governing early petal development in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 100, 8571–8576. doi: 10.1073/pnas.1033043100

PubMed Abstract | CrossRef Full Text | Google Scholar

Edgar, R. C. (2004). MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32, 1792–1797. doi: 10.1093/nar/gkh340

PubMed Abstract | CrossRef Full Text | Google Scholar

Finley, D., Ulrich, H. D., Sommer, T., and Kaiser, P. (2012). The ubiquitin-proteasome system of Saccharomyces cerevisiae. Genetics 192, 319–360. doi: 10.1534/genetics.112.140467

PubMed Abstract | CrossRef Full Text | Google Scholar

Fritsch, S., Guenther, F., and Wright, M. N. (2019). neuralnet: Training of Neural Networks. R Package Version 1.44.2. Available online at: https://CRAN.R-project.org/package=neuralnet (accessed Nov 21, 2020).

Google Scholar

Gagne, J. M., Downes, B. P., Shiu, S. H., Durski, A. M., and Vierstra, R. D. (2002). The F-box subunit of the SCF E3 complex is encoded by a diverse superfamily of genes in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 99, 11519–11524. doi: 10.1073/pnas.162339999

PubMed Abstract | CrossRef Full Text | Google Scholar

Gilkerson, J., Hu, J., Brown, J., Jones, A., Sun, T. P., and Callis, J. (2009). Isolation and characterization of cul1-7, a recessive allele of CULLIN1 that disrupts SCF function at the C terminus of CUL1 in Arabidopsis thaliana. Genetics 181, 945–963. doi: 10.1534/genetics.108.097675

PubMed Abstract | CrossRef Full Text | Google Scholar

Grau-Bove, X., Sebe-Pedros, A., and Ruiz-Trillo, I. (2015). The eukaryotic ancestor had a complex ubiquitin signaling system of archaeal origin. Mol. Biol. Evol. 32, 726–739. doi: 10.1093/molbev/msu334

PubMed Abstract | CrossRef Full Text | Google Scholar

Greer, B. T., and Khan, J. (2004). Diagnostic classification of cancer using DNA microarrays and artificial intelligence. Ann. N. Y. Acad. Sci. 1020, 49–66. doi: 10.1196/annals.1310.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Hedtmann, C., Guo, W., Reifschneider, E., Heiber, I., Hiltscher, H., Van Buer, J., et al. (2017). The plant immunity regulating F-Box protein CPR1 supports plastid function in absence of pathogens. Front. Plant Sci. 8:1650. doi: 10.3389/fpls.2017.01650

PubMed Abstract | CrossRef Full Text | Google Scholar

Hershko, A., and Ciechanover, A. (1998). The ubiquitin system. Annu. Rev. Biochem. 67, 425–479.

Google Scholar

Hua, Z. (2021). Diverse evolution in 111 plant genomes reveals purifying and dosage balancing selection models for F-box genes. Int. J. Mol. Sci. 22:871. doi: 10.3390/ijms22020871

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., and Early, M. J. (2019). Closing target trimming and CTTdocker programs for discovering hidden superfamily loci in genomes. PLoS One 14:e0209468. doi: 10.1371/journal.pone.0209468

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., Fields, A., and Kao, T. H. (2008). Biochemical models for S-RNase-based self-incompatibility. Mol. Plant 1, 575–585. doi: 10.1093/mp/ssn032

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., and Gao, Z. (2019). Adaptive and degenerative evolution of the S-phase kinase-associated protein 1-like family in Arabidopsis thaliana. PeerJ 7:e6740. doi: 10.7717/peerj.6740

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., Pool, J. E., Schmitz, R. J., Schultz, M. D., Shiu, S. H., Ecker, J. R., et al. (2013). Epigenomic programming contributes to the genomic drift evolution of the F-Box protein superfamily in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 110, 16927–16932. doi: 10.1073/pnas.1316009110

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., and Vierstra, R. D. (2011). The cullin-RING ubiquitin-protein ligases. Annu. Rev. Plant Biol. 62, 299–334.

Google Scholar

Hua, Z., and Yu, P. (2019). Diversifying evolution of the ubiquitin-26S proteasome system in Brassicaceae and Poaceae. Int. J. Mol. Sci. 20:3226. doi: 10.3390/ijms20133226

PubMed Abstract | CrossRef Full Text | Google Scholar

Hua, Z., Zou, C., Shiu, S. H., and Vierstra, R. D. (2011). Phylogenetic comparison of F-Box (FBX) gene superfamily within the plant kingdom reveals divergent evolutionary histories indicative of genomic drift. PLoS One 6:e16219. doi: 10.1371/journal.pone.0016219

PubMed Abstract | CrossRef Full Text | Google Scholar

Johansson, M., and Staiger, D. (2015). Time to flower: interplay between photoperiod and the circadian clock. J. Exp. Bot. 66, 719–730. doi: 10.1093/jxb/eru441

PubMed Abstract | CrossRef Full Text | Google Scholar

Kataria, S., Jajoo, A., and Guruprasad, K. N. (2014). Impact of increasing ultraviolet-B (UV-B) radiation on photosynthetic processes. J. Photochem. Photobiol. B 137, 55–66. doi: 10.1016/j.jphotobiol.2014.02.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Katoh, K., Rozewicki, J., and Yamada, K. D. (2019). MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. 20, 1160–1166. doi: 10.1093/bib/bbx108

PubMed Abstract | CrossRef Full Text | Google Scholar

Khan, J., Wei, J. S., Ringner, M., Saal, L. H., Ladanyi, M., Westermann, F., et al. (2001). Classification and diagnostic prediction of cancers using gene expression profiling and artificial neural networks. Nat. Med. 7, 673–679. doi: 10.1038/89044

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, D. Y., Scalf, M., Smith, L. M., and Vierstra, R. D. (2013). Advanced proteomic analyses yield a deep catalog of ubiquitylation targets in Arabidopsis. Plant Cell 25, 1523–1540. doi: 10.1105/tpc.112.108613

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, H. J., Oh, S. A., Brownfield, L., Hong, S. H., Ryu, H., Hwang, I., et al. (2008). Control of plant germline proliferation by SCFFBL17 degradation of cell cycle inhibitors. Nature 455, 1134–1137. doi: 10.1038/nature07289

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, W., and Chetelat, R. T. (2015). Unilateral incompatibility gene ui1.1 encodes an S-locus F-box protein expressed in pollen of Solanum species. Proc. Natl. Acad. Sci. U.S.A. 112, 4417–4422. doi: 10.1073/pnas.1423301112

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Z., Defoort, J., Tasdighian, S., Maere, S., van de Peer, Y., and de Smet, R. (2016). Gene duplicability of core genes is highly consistent across all angiosperms. Plant Cell 28, 326–344. doi: 10.1105/tpc.15.00877

PubMed Abstract | CrossRef Full Text | Google Scholar

Liaw, A., and Wiener, M. (2002). Classification and regression by randomForest. R News 2, 18–22.

Google Scholar

Liu, F., Ni, W., Griffith, M. E., Huang, Z., Chang, C., Peng, W., et al. (2004). The ASK1 and ASK2 genes are essential for Arabidopsis early development. Plant Cell 16, 5–20.

Google Scholar

Majee, M., Kumar, S., Kathare, P. K., Wu, S., Gingerich, D., Nayak, N. R., et al. (2018). KELCH F-BOX protein positively influences Arabidopsis seed germination by targeting PHYTOCHROME-INTERACTING FACTOR1. Proc. Natl. Acad. Sci. U.S.A. 115, E4120–E4129.

Google Scholar

Marshall, R. S., and Vierstra, R. D. (2019). Dynamic regulation of the 26S proteasome: from synthesis to degradation. Front. Mol. Biosci. 6:40. doi: 10.3389/fmolb.2019.00040

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer, D., Dimitriadou, E., Hornik, K., Weingessel, A., and Leisch, F. (2020). e1071: Misc Functions of the Department of Statistics, Probability Theory Group (Formerly: E1071), TU Wien. R Package Version 1.7-4. Available online at: https://CRAN.R-project.org/package=e1071 (accessed Nov 21, 2020).

Google Scholar

Monti, S., Tamayo, P., Mesirov, J., and Golub, T. (2003). Consensus clustering: a resampling-based method for class discovery and visualization of gene expression eicroarray data. Mach. Learn. 52, 91–118.

Google Scholar

Moon, J., Zhao, Y., Dai, X., Zhang, W., Gray, W. M., Huq, E., et al. (2007). A new CULLIN 1 mutant has altered responses to hormones and light in Arabidopsis. Plant Physiol. 143, 684–696. doi: 10.1104/pp.106.091439

PubMed Abstract | CrossRef Full Text | Google Scholar

Noir, S., Marrocco, K., Masoud, K., Thomann, A., Gusti, A., Bitrian, M., et al. (2015). The control of Arabidopsis thaliana growth by cell proliferation and endoreplication requires the F-Box protein FBL17. Plant Cell 27, 1461–1476. doi: 10.1105/tpc.114.135301

PubMed Abstract | CrossRef Full Text | Google Scholar

Pirooznia, M., Yang, J. Y., Yang, M. Q., and Deng, Y. (2008). A comparative study of different machine learning methods on microarray gene expression data. BMC Genomics 9(Suppl. 1):S13. doi: 10.1186/1471-2164-9-S1-S13

PubMed Abstract | CrossRef Full Text | Google Scholar

Qiao, H., Chang, K. N., Yazaki, J., and Ecker, J. R. (2009). Interplay between ethylene, ETP1/ETP2 F-box proteins, and degradation of EIN2 triggers ethylene responses in Arabidopsis. Genes Dev. 23, 512–521. doi: 10.1101/gad.1765709

PubMed Abstract | CrossRef Full Text | Google Scholar

Quint, M., Ito, H., Zhang, W., and Gray, W. M. (2005). Characterization of a novel temperature-sensitive allele of the CUL1/AXR6 subunit of SCF ubiquitin-ligases. Plant J. 43, 371–383. doi: 10.1111/j.1365-313x.2005.02449.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Santner, A., and Estelle, M. (2010). The ubiquitin-proteasome system regulates plant hormone signaling. Plant J. 61, 1029–1040. doi: 10.1111/j.1365-313x.2010.04112.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Sheard, L. B., Tan, X., Mao, H., Withers, J., Ben-Nissan, G., Hinds, T. R., et al. (2010). Jasmonate perception by inositol-phosphate-potentiated COI1-JAZ co-receptor. Nature 468, 400–405. doi: 10.1038/nature09430

PubMed Abstract | CrossRef Full Text | Google Scholar

Stamatakis, A. (2014). RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30, 1312–1313. doi: 10.1093/bioinformatics/btu033

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, L., Williams, J. S., Li, S., Wu, L., Khatri, W. A., Stone, P. G., et al. (2018). S-locus F-box proteins are solely responsible for S-RNase-based self-incompatibility of Petunia pollen. Plant Cell 30, 2959–2972. doi: 10.1105/tpc.18.00615

PubMed Abstract | CrossRef Full Text | Google Scholar

Tan, X., Calderon-Villalobos, L. I., Sharon, M., Zheng, C., Robinson, C. V., Estelle, M., et al. (2007). Mechanism of auxin perception by the TIR1 ubiquitin ligase. Nature 446, 640–645.

Google Scholar

Vanitha, C. D. A., Devaraj, D., and Venkatesulu, M. (2015). Gene expression data classification using Support Vector Machine and mutual information-based gene selection. Procedia Comput. Sci. 47, 13–21. doi: 10.1016/j.procs.2015.03.178

CrossRef Full Text | Google Scholar

Vierstra, R. D. (2009). The ubiquitin-26S proteasome system at the nexus of plant biology. Nat. Rev. Mol. Cell Biol. 10, 385–397. doi: 10.1038/nrm2688

PubMed Abstract | CrossRef Full Text | Google Scholar

Welchman, R. L., Gordon, C., and Mayer, R. J. (2005). Ubiquitin and ubiquitin-like proteins as multifunctional signals. Nat. Rev. Mol. Cell Biol. 6, 599–609. doi: 10.1038/nrm1700

PubMed Abstract | CrossRef Full Text | Google Scholar

Wilkerson, M. D., and Hayes, D. N. (2010). ConsensusClusterPlus: a class discovery tool with confidence assessments and item tracking. Bioinformatics 26, 1572–1573. doi: 10.1093/bioinformatics/btq170

PubMed Abstract | CrossRef Full Text | Google Scholar

Xie, D. X., Feys, B. F., James, S., Nieto-Rostro, M., and Turner, J. G. (1998). COI1: an Arabidopsis gene required for jasmonate-regulated defense and fertility. Science 280, 1091–1094. doi: 10.1126/science.280.5366.1091

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, G., Ma, H., Nei, M., and Kong, H. (2009). Evolution of F-box genes in plants: different modes of sequence divergence and their relationships with functional diversification. Proc. Natl. Acad. Sci. U.S.A. 106, 835–840. doi: 10.1073/pnas.0812043106

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, X., Kalluri, U. C., Jawdy, S., Gunter, L. E., Yin, T., Tschaplinski, T. J., et al. (2008). The F-box gene family is expanded in herbaceous annual plants relative to woody perennial plants. Plant Physiol. 148, 1189–1200. doi: 10.1104/pp.108.121921

PubMed Abstract | CrossRef Full Text | Google Scholar

Yapa, M. M., Yu, P., Liao, F., Moore, A. G., and Hua, Z. (2020). Generation of a fertile ask1 mutant uncovers a comprehensive set of SCF-mediated intracellular functions. Plant J. 104, 493–509. doi: 10.1111/tpj.14939

PubMed Abstract | CrossRef Full Text | Google Scholar

Yau, R., and Rape, M. (2016). The increasing complexity of the ubiquitin code. Nat. Cell Biol. 18, 579–586. doi: 10.1038/ncb3358

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, H., Zhang, F., Yu, Y., Feng, L., Jia, J., Liu, B., et al. (2020). A comprehensive online database for exploring approximately 20,000 public Arabidopsis RNA-Seq libraries. Mol. Plant 13, 1231–1233. doi: 10.1016/j.molp.2020.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, D., Yang, M., Solava, J., and Ma, H. (1999). The ASK1 gene regulates development and interacts with the UFO gene to control floral organ identity in Arabidopsis. Dev. Genet. 25, 209–223. doi: 10.1002/(sici)1520-6408(1999)25:3<209::aid-dvg4>3.0.co;2-o

CrossRef Full Text | Google Scholar

Zheng, N., Schulman, B. A., Song, L., Miller, J. J., Jeffrey, P. D., Wang, P., et al. (2002). Structure of the Cul1-Rbx1-Skp1-F-boxSkp2 SCF ubiquitin ligase complex. Nature 416, 703–709.

Google Scholar

Zhu, J. Y., Li, Y., Cao, D. M., Yang, H., Oh, E., Bi, Y., et al. (2017). The F-box protein KIB1 mediates brassinosteroid-induced inactivation and degradation of GSK3-like kinases in Arabidopsis. Mol. Cell 66, 648–657.e4.

Google Scholar

Keywords: Arabidopsis, F-box, UPS, activity, machine leaning, artificial neural network, expression, evolution

Citation: Li Y, Yapa MM and Hua Z (2021) A Machine Learning Approach to Prioritizing Functionally Active F-box Members in Arabidopsis thaliana. Front. Plant Sci. 12:639253. doi: 10.3389/fpls.2021.639253

Received: 08 December 2020; Accepted: 12 April 2021;
Published: 28 May 2021.

Edited by:

Matthew James Christians, Grand Valley State University, United States

Reviewed by:

Derek Gingerich, University of Wisconsin–Eau Claire, United States
Yuese Ning, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, China
Giovanna Serino, Sapienza University of Rome, Italy

Copyright © 2021 Li, Yapa and Hua. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zhihua Hua, hua@ohio.edu