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Original Research ARTICLE

Front. Plant Sci., 22 December 2017 | https://doi.org/10.3389/fpls.2017.02171

RPS9M, a Mitochondrial Ribosomal Protein, Is Essential for Central Cell Maturation and Endosperm Development in Arabidopsis

Changqing Lu1†, Feng Yu1†, Lianfu Tian1†, Xiaoying Huang1, Hong Tan1, Zijing Xie1, Xiaohua Hao1, Dongping Li1*, Sheng Luan1,2* and Liangbi Chen1*
  • 1Hunan Province Key Laboratory of Crop Sterile Germplasm Resource Innovation and Application, Hunan Normal University, Changsha, China
  • 2Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, United States

During double fertilization of angiosperms, the central cell of the female gametophyte fuses with a sperm cell to produce the endosperm, a storage tissue that nourishes the developing embryo within the seed. Although many genetic mutants defective in female gametophytic functions have been characterized, the molecular mechanisms controlling the specification and differentiation of the central cell are still not fully understood. Here, we report a mitochondrial ribosomal protein, RPS9M, is required for central cell maturation. RPS9M was highly expressed in the male and female gametophytes before and after double fertilization. The female gametophytes were defective in the rps9m mutant specifically concerning maturation of central cells. The morphological defects include unfused polar nuclei and smaller central vacuole in central cells. In addition, embryo initiation and early endosperm development were also severely affected in rps9m female gametophytes even after fertilized with wild type pollens. The RPS9M can interact with ANK6, an ankyrin-repeat protein in mitochondria previously reported to be required for fertilization. The expression pattern and mutant phenotype of RPS9M are similar to those of ANK6 as well, suggesting that RPS9M may work together with ANK6 in controlling female gametophyte development, possibly by regulating the expression of some mitochondrial proteins.

Introduction

In angiosperms, the egg and sperm cells form within the female and male gametophytes through a series of meiosis, mitosis, and cell fate determination, respectively (Ma and Sundaresan, 2010). During female gametophyte development in most flowering plants, the megaspore mother cell (MMC) undergoes meiosis to produce four haploid megaspores. Three of the megaspores undergo programmed cell death, leaving one survived megaspore to become functional megaspore (FM). Subsequently, the FM cell undergoes three rounds of mitosis without cellularization to produce an eight-nucleate structure. Then migration of nuclei and cellularizations result in a seven-celled female gametophyte consisting of one egg cell, two synergid cells, three antipodal cells, and one central cell containing two polar nuclei (Yang et al., 2010). In Arabidopsis thaliana and many other species, two polar nuclei fuse to form a diploid nucleus in the central cell and the central cell vacuole enlarged before fertilization. (Yadegari and Drews, 2004).

By genetic and molecular approaches, a number of genes have been identified to be involved in female gametophyte development (Yadegari and Drews, 2004; Kaegi and Gross-Hardt, 2007; Liu and Qu, 2008; Sundaresan and Alandete-Saez, 2010; Yang et al., 2010; Martin et al., 2014), and some of them display maternal effects on seed formation (Huh et al., 2008; Berger and Chaudhury, 2009; North et al., 2010). In the past decades or so, mutants defective in central cell development have also been described, including FEM111/AGL80 (Portereiko et al., 2006a), AGL61 (Bemer et al., 2008; Steffen et al., 2008), and the BiP genes (BiP1 and BiP2) (Maruyama et al., 2010). AGL61 and AGL80 encode the type I MADS-domain transcription factors and mutation of either of them results in smaller central cell with reduced vacuole. Consequently the central cell in either agl61 or agl80 mutant fail to give rise to endosperms after fertilization. Yeast two-hybrid (Y2H) assay show that AGL61 interact with AGL80, suggesting that these two transcription factors may function as a heterodimer in controlling the expression of downstream genes during central cell development. The BiP genes encode molecular chaperones of the Hsp70 family in the endoplasmic reticulum. The central cell in bip1bip2 double mutant show defects in the fusion of polar nuclei, which may result from altered nuclear membrane. After fertilization, the mutant shows aberration in endosperm nuclear division, indicating that central cell maturation plays an important role in endosperm development.

Mitochondria also play a critical role in female gametophyte maturation. Mutations in some genes encoding mitochondrial proteins cause defects in female gametophyte. These include RPL21M/NFD1 (Portereiko et al., 2006b), FIONA/SYCO (Kaegi et al., 2010), GCD1 (Wu et al., 2012) and MSD1/OIWA (Martin et al., 2013). RPL21M encodes the mitochondrial 50S ribosomal subunit L21 and is essential for the fusion of polar nuclei during female gametophyte maturation and the male-female gametophyte recognition during double fertilization. FIONA encodes the cysteinyl t-RNA synthetase and requires for the central cell development and mitochondrial cristae integrity. GCD1 encodes the ribosomal protein L20 which is enriched in gametophytes and plays important roles in fusion of polar nuclei, maturation of female gametes, embryogenesis initiation, and endosperm development. MSD1 encodes a mitochondrial Mn-superoxide dismutase, which is critical for distribution of reactive oxygen species (ROS) during embryo sac patterning. All these genes described above are important for central cell maturation and endosperm development, indicating the importance of mitochondria in female gametophyte maturation.

Our previous work identified ANK6 gene as required for male–female gamete recognition. ANK6 is an ankyrin protein located in the mitochondria and likely functions as a scaffold to mediate protein–protein interactions through its ankyrin repeat domains. Indeed, we found a member of σ-transcription initiation factor, SIG5, as a partner for ANK6. Like in ank6 mutant, a proportion of sig5 embryo sacs are also arrested at late stages of female gametophyte development (Yu et al., 2010). In the same yeast two hybrid screen, a mitochondrial ribosomal small subunit protein, designated RPS9M, showed interaction with ANK6. RPS9M is highly expressed in both male and female gametophytes just like ANK6. The rps9m mutants have female gametophyte defects and, in particular, the central cells showed smaller vacuoles and defect in the fusion of polar nuclei. Although rps9m embryo sacs are capable of double fertilization, embryogenesis initiation and endosperm proliferation are both defective after fertilization whether mutant or wild type pollens are used for pollination. Together, these results suggest that RPS9M functions with ANK6 and possibly other proteins (e.g., SIG5) in the control of mitochondrial gene expression during female gametophyte.

Materials and Methods

Plant Materials and Growth Conditions

Arabidopsis thaliana (ecotype Columbia-0) plants were used in this study unless otherwise indicated. Seeds were surface sterilized in 70% ethanol for 5 min, stratified at 4°C for 2 days, and grown on half-strength Murashige and Skoog (Sigma1) medium at 22°C under 16:8 h light: dark cycles for a week. Then plants were transferred to soil and incubated in a constant-temperature room at 22°C under 16 h light/8 h dark cycles. Agrobacterium-mediated transformation were as described previously (Clough and Bent, 1998). The transgenic lines were selected on 0.5 × Murashige and Skoog medium (Sigma) containing 50 μg/mL kanamycin (for pBI101-based vectors) or 30 μg/mL hygromycin B (for pCAMBIA 1300-based vectors).

Plasmid Constructs

The RPS9M cDNA is amplified by RT-PCR using the primer pair RPS9M-F and RPS9M-R and ligated into the pMD18-T vector (TaKaRa). To make the ProRPS9M-GUS construct for histochemical analysis, a 2.2-kb fragment upstream of the ATG starting codon of RPS9M was PCR amplified using the primers RPS9M-PF and RPS9M-PR and cloned into the pMD18-T vector, then subcloned into the pBI101.2 vector using the same primers. For subcellular localization analysis, the RPS9M CDS was amplified without its stop codon using the primer pair RPS9M-GF and RPS9M-GR, subsequently digested with Xba I and BamH I, respectively, and then inserted into the plant binary vector pMD1-GFP to make the 35S-RPS9M-GFP fusion construct.

For CRISPR/Cas9 plant expression vectors construction. The chimeric sgRNA for RPS9M was constructed by cloning annealed oligos RPS9M-sgF and RPS9M-sgR into pBlueScript SK-sgRNA, then both the sgRNA and hSpCas9 were subcloned into the expression vector pCAMBIA1300 (Supplementary Figure S2A) as previously described (Feng et al., 2013; Mao et al., 2013).

Histochemical GUS Analysis

Transformed Arabidopsis lines carrying the pRPS9M-GUS fusion were selected based on Kanamycin resistance. The promoter activity was reflected by GUS activity visualized in the plant tissues using 5-bromo-4-chloro-3-indolylb-D-glucuronide (X-Gluc) as a substrate according to published protocols (Jefferson et al., 1987). In details, inflorescences and 2 week old seedlings were incubated in GUS staining solution [10 mg/mL X-Gluc, 0.1 M K3(Fe(CN)6), 0.1 M K4Fe(CN)6⋅3H2O, 1 M Na2EDTA, 0.2 M Na3PO4 (pH7.0)] at 37°C overnight. Then the plant tissues were decolorized for 30 min in each of the gradient ethanol solution (30, 40, 50, 60, 70%) and incubated in 75% ethanol at 37°C overnight. The samples were examined and photographed with an Olympus SZX12 microscope equipped with a camera.

Yeast Two-Hybrid (Y2H) Screen and Analysis

We used the CLONTECH Matchmaker GAL4 Two-Hybrid System 3 for the yeast (Saccharomyces cerevisiae) two-hybrid screen and analysis. For performing Y2H screen of Arabidopsis cDNA library, according to the method described as previous (Yu et al., 2010). The ANK6 CDS were fused to GAL4 DNA-binding domain in pGBKT7. AH109 cells were first transformed with pBD-ANK6 plasmid, then the transformants were transformed with the Arabidopsis cDNA library cloned in the prey vector pACT. The transformed cells were plated on synthetic dropout (SD) selection medium that lacked Trp, Leu, and His supplemented with 20 mM 3-AT to reduce the growth of false-positive colonies. The plates were incubated at 30°C for 3–12 days. The prey plasmid DNAs were isolated from yeast, transformed and isolated from Escherichia coli, and retransformed into yeast cells containing either the empty vector or the vector with bait to verify growth further. The clones that continued to grow in the -His and +3-AT medium after retransformation were selected for DNA sequencing. For Y2H analysis the interactions between RPS9M and ANK6, the RPS9M CDS and truncated RPS9M variants were fused to the GAL4 activation domain in pGADT7. Yeast strain AH109 was cotransformed with combinations of pGADT7 and pGBKT7 constructs and selected on SD medium lacking Leu and Trp (SD-LW). Cotransformants were then assayed for interaction and activation of the His and adenine reporter genes on SD medium lacking Leu, Trp, His, and adenine (SD-LWHA). For this, fresh colonies were grown in SD-LW at 30°C overnight to an OD600 of 1–2, the cells were pelleted and resuspended in 0.5 M sorbitol to an OD600 of 0.5, and 5 μL of each cell suspension was spotted on SD-LWHA plates using a multichannel pipette and grown at 30°C for 2–3 days.

Bimolecular Fluorescence Complementation (BiFC) Assays

The ORF sequence of ANK6 and RPS9M was cloned into the plasmid pE3308 and pE3449 using the primer pairs list in Supplementary Table S2. Protoplasts were isolated from 4 week old Arabidopsis rosette leaves. Transient protoplast expression was performed using the polyethylene glycol transformation method as described previously (Sheen, 2001).

CLSM and Central Cell Vacuole Size Calculation

The confocal observation of ovules was performed according to the method described previously (Christensen et al., 1997) with slight modifications. Inflorescences were harvested and fixed in 4% glutaraldehyde (in 12.5 mM cacodylate, pH 6.9), and a vacuum was applied for the initial 20 min, after which they were in fixative overnight at room temperature. After fixation, the tissues were dehydrated through a conventional ethanol series with 20 min per step. After the dehydration, the tissue was cleared in 2:1 (v/v) benzyl benzoate: benzyl alcohol for a minimum of 1 h. Pistils or siliques were dissected, mounted with immersion oil, and observed with a Zeiss LSM510 META laser scanning microscope (Zeiss, Jena, Germany) with a 488-nm argon laser and an LP 530 filter. Images were edited with Zeiss LSM Image Browser software and Photoshop software. The central cell vacuole size was calculated according to the method as described previously (Wu et al., 2012). Single section image was captured when scanning to the largest sectional view of the central cell vacuole, and the size of central cell vacuoles were calculated using Image J software.

Results

RPS9M Interacts with Ankyrin Protein ANK6

The ankyrin repeats are generally recognized as protein–protein interaction modules. We previously showed that mitochondrial ANK6 protein functions in double fertilization, suggesting that a protein complex mediated by this ankyrin repeat protein might participate in ovule development. We performed a Y2H screening by using ANK6 (amino acid residues 21–174) as a bait to screen a prey cDNA library. Several positive clones were obtained, including RPS9M, a bacterial-origin mitochondrial-type ribosomal protein S9 gene (AT3G49080) (Bonen and Calixte, 2006). It encodes a 430-aa protein, with a Ribosomal_S9 domain at the C terminus (amino acid residues 310–430) and a non-conserved region at the N-terminus, according to the SMART protein domain prediction program (Figure 1A). The sequence of the Ribosomal_S9 domain shows high similarity to the RPS9 protein of Escherichia coli and chloroplast ribosomal protein S9 of Arabidopsis. To identify the ANK6-interacting domain, three truncated RPS9M variants were fused with GAL4 activation domain (Figure 1A). The interaction between these variants and ANK6 were assayed by using the Y2H system (Figure 1B). ANK6 interacts with the C-terminus Ribosomal_S9 domain of RPS9M. RPS9M lacking the non-conserved N-terminus showed a reduced interaction activity with ANK6, suggesting a role for the N-terminus in regulating the interaction of RPS9M with ANK6 (Figure 1).

FIGURE 1
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FIGURE 1. Interaction between RPS9M and ANK6 determined by Y2H analysis. (A) Diagram of the full-length and truncated RPS9M constructs with specific deletions. (B) Y2H analysis of ANK6 interacting with full-length and truncated RPS9M.

RPS9M Is a Mitochondrial Localized Protein and Interacts with ANK6 in Mitochondria

The RPS9M protein contains a mitochondrial pre-sequence that targets the protein to mitochondria according to SUBAcon. To investigate the subcellular location, an RPS9M-GFP gene cassette driven by the cauliflower mosaic virus 35S promoter was constructed and introduced into wild type plants (Supplementary Figure S4). The GFP fluorescent signals were detected in the roots of these transgenic plants under confocal microscopy. MitoTracker dye was used as a control to stain mitochondria of the roots. In the root epidermal cells of a 35S-RPS9M-GFP line, the green fluorescent signals were colocalized with the MitoTracker fluorescent signals (Figure 2A), indicating that RPS9M protein was targeted to mitochondria.

FIGURE 2
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FIGURE 2. The subcellular localization of RPS9M in plant and interaction between RPS9M and ANK6 determined by BiFC analysis in mesophyll protoplasts. (A) Subcellular localization of RPS9M. From left to right, MitoTracker, GFP fluorescence and merged images. (B) The interaction between RPS9M and ANK6 determined by BiFC analysis in mesophyll protoplasts. Full-length RPS9M protein was fused to C-terminal CFP (CFPC), and full-length ANK6 was fused to N-terminal Venus (VenusN). Mesophyll protoplasts were cotransfected with the RPS9M-CFPC and ANK6-VenusN fusion constructs (Upper) or with the RPS9M-CFPC fusion and VenusN construct (Lower). From left to right, YFP signals (green, observed with GFP filter), MitoTracker (red) stained mitochondria, merged images and DIC. Bars = 20 μm.

To confirm the interaction between RPS9M and ANK6, we performed bimolecular fluorescence complementation assays in plant cells. We co-expressed RPS9M tagged with C-terminal CFP and ANK6 tagged with N-terminal Venus in mesophyll protoplasts. The yellow/green fluorescence signals indicated interaction between RPS9M and ANK6. Mitochondrial dye was used to localize mitochondria. As shown in Figure 2B, the yellow/green fluorescence and the red dye signals were overlapped, supporting the notion that RPS9M and ANK6 interact with each other in mitochondria.

RPS9M Is Expressed in Both Male and Female Gametophyte

In order to reveal the function of RPS9M gene, we first examined the expression pattern of RPS9M using transgenic plants harboring the reporter construct with RPS9M promoter fused to the β-glucuronidase (GUS) gene. Seven GUS transgenic lines were selected and their GUS activities were identified with similar expression patterns. Strong GUS activities were detected in inflorescence particularly in the anthers and pistils of T2 transgenic lines (Figure 3A and Supplementary Figures S1A,B). In anthers, GUS activities were detected throughout the developmental stages, especially in the mature pollen grains (Figure 3B and Supplementary Figures S1A,B). In pistils, GUS activities were detected in female gametophytes at different developmental stages (Figures 3C–G), particularly in the mature female gametophyte stage (Figure 3F). The RPS9M promoter was also highly active during double fertilization (Figure 3G). After fertilization, GUS signals were detected in young siliques, especially in embryo and endosperms (Supplementary Figures S1B,D,E), but no GUS signal was detected in mature seeds (Supplementary Figure S1C). GUS signals were also observed in young leaves and root tips (Supplementary Figure S1F). These expression patterns suggest that RPS9M may participate in the development of male and female gametophytes as well as in embryogenesis.

FIGURE 3
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FIGURE 3. Expression patterns of RPS9M by GUS reporter analysis. Histochemical analysis of RPS9M promoter-driven GUS reporter expression in transgenic Arabidopsis plants. GUS signals (indicated in blue) were observed in inflorescence (A), pollen grains (B) and different developmental stages of female gametophytes (C–G). Inflorescence (A), mature pollen grains (B), FG1 stage (C), FG2-FG3 stage (D), FG4 stage (E), FG5–FG7 stage (F), ovule with penetrating pollen tube (PT, arrow) (G). Bars = 5 mm (A) and 20 μm (B–G).

RPS9M Mutant Displayed Empty Seed Sets in Siliques

To determine the function of RPS9M gene in plant development, CRISPR/Cas9 gene editing approach was adopted to produce mutations in the RPS9M gene (Jiang et al., 2013; Mao et al., 2013; Zhang et al., 2014). We designed two sgRNA that targeted the coding sequence of RPS9M gene and transformed into wild type plants. A series of heterozygous mutants were obtained in the T1 generation. Most of the mutants involved insertions or deletions of a few nucleotides, with rare cases of sizable deletions of 30 or more nucleotides (Supplementary Figures S2B–D). In this study we chose two mutant lines for further research, one contain a deletion of 32 nucleotides, equivalent to the sequence of +271–+302 (named as rps9m-1) and the other contain a deletion of 5 nucleotides equivalent to the sequence of +375–+379 (named as rps9m-2) (Figure 4A). Genetic segregation in T2 generation produced mutant plants that did not contain T-DNA insertion sequences or sgRNA/Cas9 fragments. Genotyping of +/rps9m-1 and +/rps9m-2 in T3 and T4 generation led to identification of several heterozygous mutant plants, but no homozygous mutant plants. No homozygous mutant was obtained even after +/rps9m plants were selfed, implying that the rps9m mutant allele may cause gametophyte defect or homozygous embryo lethality. The heterozygous plants grew normally in the vegetative stage. However, after fertilization, about 50% ovules in both +/rps9m-1 and +/rps9m-2 siliques were aborted at early stage (Figures 4B,C). Analysis of the progeny of +/rps9m-1 and +/rps9m-2 plants and other mutant lines in T4 generation revealed a segregation ratio of wild type to heterozygous plants close to 1:0.2 (Supplementary Table S1). These data suggested that not only the female gametophyte, but also the male gametophyte were defective when RPS9M function was disrupted.

FIGURE 4
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FIGURE 4. Phenotypic observation of +/rps9m siliques. (A) Schematic diagram of RPS9M gene structure and the mutation position in rps9m-1 and rps9m-2 mutant. The ATG start codon and TGA stop codon are shown as indicated. The mutation position and deleted nucleotides was determined to the first exon by PCR and sequencing (triangle above the gene diagram). (B) Phenotype of the +/rps9m plant. In contrast to wild type (upper), half of seeds in selfed +/rps9m-1 and +/rps9m-2 siliques were aborted during development (arrowheads, middle), whereas the complemented transgenic plants of rps9m-1 and rps9m-2 (RPS9MC1 and RPS9MC2) recovered the phenotype to the wild type level (lower). (C) Frequencies (%) of the aborted seeds in per silique of wild type, +/rps9m-1, +/rps9m-2 and RPS9MC1 and RPS9MC2 plants. Error bars represent ± SD.

To further examine the function of RPS9M in reproduction, reciprocal cross-tests between the heterozygous +/rps9m-1 mutant and wild type plants were performed. When +/rps9m-1 pistils were pollinated with wild type pollens, only a few heterozygote plants were identified in the progeny, the transmission of rps9m-1 allele through female gametophyte was reduced to 3% (n = 151; P< 0.001) (Table 1). In addition, siliques resulting from this cross exhibited about 50% aborted seed sets. These observations indicate that RPS9M lose-of-function mutation almost completely disrupt the female gametophyte function. When wild type ovules were pollinated with +/rps9m-1 pollens, we found the transmission efficiency of the rps9m-1 male gametophyte was significantly reduced (TE = 21%; n = 167; P< 0.001), compared with that of the wild type allele (Table 1), indicating that the male gametophyte function is also affected, albeit to a lesser extent compared to the defect of the female gametophyte. Similar results were obtained when reciprocal cross-tests were done between +/rps9m-2 and wild type plants that the transmission of female gametophyte was almost completely blocked and the transmission of male gametophyte was reduced to 24% (Table 1). These results demonstrate that loss of RPS9M function indeed cause defects in both two gametophytes, especially the female gametophyte.

TABLE 1
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TABLE 1. Transmission of rps9m alleles to F1 progenies after reciprocal crosses.

To verify that the observed phenotypes were caused by loss-of-function of the AtRPS9M gene, we performed genetic complementation experiment by introducing 35S-RPS9M-GFP construct into +/rps9m-1 and +/rps9m-2 mutant plant. In the T2 populations, we obtained 5 independent lines that were homozygous for both the rps9m-1 allele and the RPS9M transgene, and 3 independent homozygous lines for rps9m-2 and RPS9M transgene. In the progenies of these transgenic lines, silique seed sets were fully restored to the wild type level (Figures 4B,C), demonstrating that the RPS9M transgene fully complemented the rps9m phenotype.

Female Gametophyte Development Is Affected in rps9m Mutants

Genetic analysis of the rps9m mutant suggested a defect in female gametophyte function. To further examine this defect, we monitored ovule development in wild type and +/rps9m plants by using whole-mount clearing and confocal laser scanning microscopy (CLSM). We first analyzed female gametophytes at the terminal development stage (stage FG7). We emasculated the wild type, +/rps9m-1 and +/rps9m-2 flowers (stage 12c) and kept them growing for 24 h, then fixed the ovule tissues for confocal analysis. Wild type female gametophytes at this stage have one egg cell, one central cell, and two synergid cells, whereas the three antipodal cells were undetected. The two polar nuclei have fused to form a diploid nucleus in most of the central cells (Figure 5A).

FIGURE 5
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FIGURE 5. The observation of central cell development in rps9m female gametophyte by CLSM. (A) Wild type female gametophyte at FG7 stage. The female gametophyte contains two synergid nucleus, one egg nucleus and a secondary central cell nucleus. (B) The rps9m-1 female gametophyte at the same pistil. The two polar nucleus still unfused and the central cell vacuole is smaller compared to that in wild type. (C) The rps9m-2 female gametophyte at the same stage. (D) Frequencies (%) of unfused polar nuclei in wild type, +/rps9m-1, +/rps9m-2 and the complemented transgenic plants of +/rps9m-1 and +/rps9m-2 at this stage. (E) The central cell vacuole size of wild type, rps9m-1 and rps9m-2. CN, central cell nucleus; EN, egg cell nucleus; PN, polar nucleus; SN, synergid nucleus; V, vacuole. Error bars represent ± SD. Bars = 10 μm. ∗∗P< 0.05, Student’s t-test.

On the other hand, ovules in +/rps9m-1 and +/rps9m-2 heterozygous flowers at the same stage showed differences from the wild type. Specifically, about 47% (n = 720) ovules in +/rps9m-1 plants and 45% (n = 630) embryo sacs in +/rps9m-2 pistils contained unfused polar nuclei (Figures 5B–D), indicating defections of polar nuclei fusion in rps9m female gametophytes. In addition, we measured the central cell vacuole size in the embryo sacs, as shown in Figure 5E, the wild type central cell vacuole size at this stage usually developed to about 510 μm2, but in rps9m sacs, the size of central cell vacuole was only about 390 μm2 in rps9m-1 and 365 μm2 in rps9m-2 which were significantly smaller than those of wild type. We next observed the morphology of egg cells and synergid cells, no obvious difference was found among rps9m-1, rps9m-2 and wild type (Figures 5A–C and Supplementary Table S4). These observations suggesting that disruption of RPS9M inhibited fusion of polar nuclei and affected central cell maturation. To further exclude the possibility that RPS9M affects the earlier developmental stages of female gametophyte, we examined female gametophytes from flowers at earlier development stages. No phenotypic variations appeared between wild type and rps9m ovules during nuclear mitosis stages (Supplementary Figure S3 and Supplementary Table S3), indicating that macrospore nuclear proliferations and migrations were not affected in rps9m female gametophytes.

Together, the data above indicate that the mutation of RPS9M specifically affects the final maturation process of the central cell during female gametophyte development.

Pollen Tube Guidance and Fertilization Is Not Impaired in rps9m

Several studies show that central cell defects sometimes affect other processes, such as pollen tube guidance and fertilization (Christensen et al., 2002; Portereiko et al., 2006b; Chen et al., 2007). In order to test whether rps9m embryo sacs affect pollen tube guidance, pollens from a transgenic line expressing pLAT52-GUS were used as donors to pollinate wild type, +/rps9m-1 and +/rps9m-2 pistils (Twell et al., 1989). The ovules were collected and GUS activities were analyzed at 24 h after pollination. Almost all ovules in wild type (96%, n = 190), +/rps9m-1 (93%, n = 240) and +/rps9m-2 (94%, n = 220) pistils had a pollen tube entered (Figure 6A), indicating that pollen tube guidance was not impaired in rps9m female gametophyte. To further investigate whether mutation of RPS9M in female gametophyte impact fertilization process, a transgenic line expressing pHTR10-mRFP1, a sperm-nuclear protein labeling monomeric red fluorescent protein, was used as pollen donors (Ingouff et al., 2007). We pollinated wild type, +/rps9m-1 and +/rps9m-2 pistils with pHTR10-RFP1 pollens. By 12 h after pollination, the RFP signals can be detected in 93% (n = 96) ovules of wild type, 89% (n = 117) ovules of +/rps9m-1 and 90% (n = 120) ovules of +/rps9m-2 plants at positions of the egg cell and central cell (Figure 6B), indicating disruption of RPS9M in female gametophyte does not impact pollen tube reception and sperm cell migration. The possibility of fertilization was evaluated by duration of RFP signals in rps9m female gametophyte after pollination, since the RFP signals elapsed quickly as soon as the fertilization was completed. About 1–2 days after pollination, no RFP signals can be detected in both wild type and rps9m female gametophytes, suggesting the double fertilization process is completed in not only wild type but rps9m female gametophytes as well. To ascertain that the double fertilization occurred in rps9m female gametophyte, a transgenic line expressing DNA LIGASE 1 nuclear protein and green fluorescent protein (GFP) fusion protein is used as paternal line (Ingouff et al., 2009). We therefore pollinated +/rps9m-1, +/rps9m-2 and wild type pistils with pollens containing LIG1-GFP. Up to 1 days after pollination (DAP), the paternal expression of LIG1-GFP labeled both the embryo and endosperm in seeds produced from WT (95%, n = 135), +/rps9m-1 (94%, n = 170) and +/rps9m-2 (96%, n = 174) pistils (Figure 6C), indicating double fertilization is not affected in rps9m female gametophyte.

FIGURE 6
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FIGURE 6. The observation of the pollen tube guidance of rps9m female gametophytes. (A) The attraction of rps9m female gametophyte to pollen tube determined by GUS reporter. Wild type and +/rps9m pistils were pollinated with LAT52-GUS pollens. Pollen tube entry into the female gametophytes was visualized by GUS staining at 1 DAP (black arrowheads). The percentages of GUS positive ovules per pistil in wild type and +/rps9m are shown. (B) The attraction of rps9m female gametophyte to pollen tube determined by RFP reporter. The pistils of wild type and +/rps9m plant were pollinated with pollens expressing sperm-specific marker HTR10-mRFP. Ovules were dissected from the pistils and observed by CLSM at 8–10 h after pollination. The arrowheads show two fertilized sperm nuclei. And the percentages of RFP positive ovules per pistils in wild type and +/rps9m were shown. (C) The fertilization of rps9m female gametophyte to sperms determined by GFP reporter. The pistils of wild type and +/rps9m plant were pollinated with LIG1-GFP pollens. Ovules were dissected from the pistils and observed at 24 h after pollination. The fertilized embryo or zygote are shown (white arrowheads) and endosperm nuclei are visible (red arrowheads). PT, pollen tube. Error bars represent ± SD. Bars = 20 μm.

Embryogenesis and Endosperm Proliferation Are Defective in rps9m Mutants

In wild type ovules, fertilized egg cell (zygote) undergoes mitosis to form the embryo and the fertilized central cell gives rise to endosperm following fertilization, ultimately developing into mature seeds. But in +/rps9m-1 siliques approximately 50% seeds aborted, the observed seed abortion phenotype was probably due to abnormal development of the embryo and/or the endosperm (Yadegari and Drews, 2004; Berger et al., 2006). We therefore analyzed embryo and endosperm development in +/rps9m-1 siliques at different time points after pollination. Briefly, the +/rps9m-1 flowers were self-pollinated. By 2 days after pollination (DAP), 91.2% of the young seeds (n = 437) contained both an embryo and endosperms. However, 41.5% of the seeds were quite different from the other half in size and endosperm cavity (Table 2). The wild type endosperm usually had 16 or more endosperm nuclei. In contrast, majority of the mutant endosperms only had two (19.5%) or four (14.6%) nuclei, and about 7.4% mutant endosperm arrested immediately. The mutant embryo development was also arrested, about 22% of the embryos arrested at the zygote stage, and 19.6% of them divided once to produce a 2-cell embryo before arrested in +/rps9m-1 silique (Figures 7A–D and Table 2). At 3 DAP, the aborted seeds collapsed. Similar results were observed from the analysis of +/rps9m-2 plants that half of seeds were aborted, and the endosperms arrested at two (17%) or four (21%) nuclei stage in the aborted seeds (Table 2). When we pollinated +/rps9m-1 and wild type ovules with LIG1-GFP pollens, at 2 DAP, the paternal expression of LIG1-GFP was detected in both the embryo and endosperms in seeds produced from wild type and +/rps9m-1 plants. But in +/rps9m-1 siliques, nearly half of seeds were aborted at the same stage as we observed in +/rps9m-1 self-pollination siliques (Figures 7E–H and Table 2). On the other hands, when +/rps9m-1 pollens were used to pollinate wild type stigmas, embryo and endosperm developed normally (Figures 7I,J and Table 2). These results suggest that defects in female gametophyte lead to seed abortion in +/rps9m-1 plants. When we pollinated WT and +/rps9m-1 pistils with pRPS9M-GUS pollens. The paternally derived pRPS9M-GUS was expressed in the zygote and endosperms soon after fertilization in both wild type and rps9m-1 ovules (Figures 7K,L), indicating the expression of the RPS9M allele in +/rps9m-1 ovule is not silenced epigenetically.

TABLE 2
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TABLE 2. Percentage of aborted endosperm and embryo in rps9m mutant.

FIGURE 7
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FIGURE 7. The zygote and early endosperm development in rps9m ovules after fertilization. (A–D) Observation of embryo and endosperm development in +/rps9m-1 siliques after fertilization. Pistils of +/rps9m-1 plant were pollinated with +/rps9m-1 pollens, and the seeds were observed at 2 DAP by CLSM. (A) Wild type seed showed normal embryo development and endosperm proliferation. (B) The seed arrested immediately after fertilization in +/rps9m-1 silique. (C) The seed arrested at zygotic embryo stage contain two endosperms in +/rps9m-1 silique. (D) The seed arrested at two-celled proembryo stage with four endosperms from +/rps9m-1 siliques. (E–H) Pistils of +/rps9m-1 plant were pollinated with wild type pollen expressing nucleus-specific marker LIG1-GFP. Ovules were dissected from the pistils and observed by CLSM at 2 DAP. GFP signals can be detected in all fertilized ovules. The RPS9M ovules developed normally (E), but rps9m-1 ovules arrested at different stages (F–H). (I,J) Seeds development after wild type female gametophytes were fertilized with +/rps9m-1 pollens. Both embryo and endosperms developed normally in wild type (I) and +/rps9m-1 (J) seeds. (K,L) GUS staining of paternal expression of pRPS9M-GUS in the developing seeds. The wild type (K) or rps9m-1 (L) female gametophyte were pollinated with pRPS9M-GUS pollens, and observed at 1 DAP. The red arrows indicate the embryos; the white arrowheads indicate the endosperm nuclei. Bars = 20 μm.

Discussion

In plants and animals, mutants of ribosomal protein genes display various specific developmental defects (Byrne, 2009; Gilbert, 2011; Horiguchi et al., 2011, 2012; Terzian and Box, 2013). Phenotypic diversity of ribosomal protein mutants may result from different patterns of gene expression or extraribosomal function of some ribosomal proteins (Ferreyra et al., 2010). Mitochondrion as a semi-autonomous organelle also contains ribosome to translate proteins encoded by mitochondrial genome. In Arabidopsis, several mutants in mitochondrial ribosomal protein genes have been reported (Portereiko et al., 2006b; Zhang et al., 2015). However, most of the mitochondrial ribosomal protein genes are still not functionally characterized. Here, we identified a mitochondrial ribosomal protein RPS9M that plays an important role in polar nuclei fusion, central cell development and endosperm proliferation. RPS9M physically interacts with ANK6, an ankyrin-repeat protein in mitochondria previously reported to be required for female gametophyte development and fertilization (Yu et al., 2010), suggesting that RPS9M may work together with ANK6 in controlling female gametophyte development.

Genetic characterization of heterozygous +/rps9m mutant plants indicates that rps9m mutation affects female gametophyte development. At the last development stage of rps9m female gametophyte, the two polar nuclei fail to fuse into one and the central cell vacuole is smaller than that in wild type (Figure 5). Lacking RPS9M probably leads to general dysfunction of mitochondria. Besides RPS9M, mutations in several other mitochondrial ribosomal proteins also caused gametophytic or seed development defects. These include HUELLENLOS (Skinner et al., 2001), RPS11 (NFD3) (Portereiko et al., 2006b), RPL21M (NFD1) (Portereiko et al., 2006b) and RPL18 (HEART STOPPER, HES) (Zhang et al., 2015). HUELLENLOS encode a mitochondrial ribosomal protein L14 that is homologous to eubacterial ribosome protein L14 and containing high similarity to cytosolic L23 and chloroplast ribosome L14 protein in Arabidopsis; mutation of HUELLENLOS lead to integuments reduced or absent, and ovule primordia collapse. Disruption of RPS11 and RPL21M both cause polar nuclei fusion defection; moreover, rpl21m female gametophyte have a defect in fusion of sperm nuclei in both the egg cell and the central cell during fertilization. HEART STOPPER (HES) encode a mitochondrial ribosomal L18 protein, hes mutant showed no defections during gametophyte development but seed development was affected, embryos were arrested at the late globular stage and endosperms uncellularized in homozygous hes mutant seeds. Silencing of the nuclear RPS10 gene disturbs the ratio between the small and large subunits of mitochondrial ribosome and changes the efficiency of translation of mRNAs for OXPHOS and ribosomal proteins (Kwasniak et al., 2013). Considering that RPS9M is a component of the mitoribosome, disruption of RPS9M may impact the integrity or stability of mitoribosome and thereby reducing the translation efficiency of some mitochondrial genes involved in mitochondrial function such as ATP synthesis, and ultimately affecting gametophyte development.

Although RPS9M is expressed in female gametophyte tissues throughout the developmental stages (Figure 3), disruption of RPS9M only impacts central cell development. No obvious morphological defects are observed in other cells such as egg cell and synergid cells of the rps9m female gametophyte (Figure 5). One plausible explanation for this phenomenon is that mutation of RPS9M impacts energy supply from mitochondria. The early development of rps9m female gametophyte is normal as the wild type mitochondria from the diploid MMC provide sufficient nutrients (ATPs, carbon skeletons) to the mutant female gametophyte. However, along with the further development of the rps9m female gametophyte, the new-born mitochondria have defect in energy supply. Inside the wild type embryo sac, the distribution of mitochondria is not uniform but largely concentrated in the central cell, whereas the egg cell and synergid cells contain only a few of mitochondria (Martin et al., 2014), suggesting that the central cell may need more energy for its development. The mutant central cell suffers more severely than other cells in the rps9m female gametophyte possibly due to defects in mitochondria failing to produce enough energy for polar nuclei fusion and central cell development.

Our data show that rps9m female gametophytes can be successfully fertilized (Figure 6), but the endosperm proliferation and embryo initiation were arrested after fertilization even when rps9m ovules were fertilized with wild type pollens (Figure 7), indicating that central cell development is critical for early endosperm development and embryo initiation. Recent studies provide evidence for the maternal control over embryogenesis and endosperm development in plant (Xin et al., 2012; Baroux and Grossniklaus, 2015). During central cell maturation, high levels of metabolic activities, large number of mitochondria, and enriched starch and lipid reserves are detected (Liu et al., 2010), suggesting that the central cell is primed for the immediate endosperm proliferation upon sperm cell delivery. But in rps9m ovules, the central cell maturation processes are defective and these may directly affect this “priming” process for endosperm development. Our data showed that the paternal-derived de novo RPS9M transcripts were detected in the zygote and endosperm cells immediately after fertilization in both rps9m ovules and wild type ovules, indicating that embryo initiation and endosperm development are independent of paternal source of RPS9M protein. Thus, the seed development defect in rps9m mutant may suffer from early defects in rps9m female gametes, which cannot be compensated by later supply of the RPS9M protein(s).

RPS9M physically interacts with ANK6 both in vitro and in vivo (Figures 1, 2B), suggesting that they are members of a protein complex in mitochondria during female gametophyte development. As an adaptor protein, ANK6 is presumed to mediate protein–protein interactions through its ANK repeat motifs, suggesting that more mitoribosomal proteins or other proteins may be recruited by ANK6 to work together with RPS9M during gametophyte developmental processes. In our previous work, an RNA polymerase transcription initiation factor, SIG5, was proven to physically interact with ANK6 in mitochondria, and the sig5 ovules also show female gametophyte defections as ank6, indicating they are essential proteins in female gametophyte development (Yu et al., 2010). In eubacteria, the transcription of mRNAs and translation of protein processes are coupled, and some proteins and complexes including RNA polymerase subunits and cofactors may be involved in both transcription and protein synthesis (Kaczanowska and Ryden-Aulin, 2007). Future work will test the hypothesis that coupled transcription/translation processes in plant mitochondria may be operated by an complex, including SIG5 and RPS9M working together, to control the transcription and translation of some mitochondrial gene(s) during gametophyte development and fertilization.

Accession Numbers

The accession numbers for the genes used for this article are as follows: At3g49080 (AtRPS9M), At5g61230 (AtANK6), and At5g24120 (AtSIG5).

Author Contributions

CL, FY, LC, SL, and DL designed the research. CL, FY, LT, XyH, HT, ZX, and XhH performed the research. CL, FY, LT, DL, SL, and LC analyzed data and wrote the paper.

Funding

This work was supported by grants of NSFC (31570316; 31371244), HNNSF (2016JJ2089), Project of Hunan Provincial Education Department (13C638), Hunan Provincial Construct Program of the Key Discipline in Ecology (0713), Hunan Provincial Cooperative Innovation Center of Engineering and New Products for Developmental Biology (20134486), and Hunan Provincial Innovation Foundation for Postgraduate (CX2014B197).

Conflict of Interest Statement

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.

Acknowledgments

The authors are grateful to Jiankang Zhu for providing CRISPR/Cas9 system. They thank Dr. Weicai Yang and Dr. Dongqiao Shi for assistance in CLSM assay, and Dr. Legong Li for assistance in BiFC analysis.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2017.02171/full#supplementary-material

Footnotes

  1. ^ www.sigmaaldrich.com

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Keywords: Arabidopsis thaliana, central cell, embryo, endosperm, female gametophyte, mitochondrion, ribosomal protein

Citation: Lu C, Yu F, Tian L, Huang X, Tan H, Xie Z, Hao X, Li D, Luan S and Chen L (2017) RPS9M, a Mitochondrial Ribosomal Protein, Is Essential for Central Cell Maturation and Endosperm Development in Arabidopsis. Front. Plant Sci. 8:2171. doi: 10.3389/fpls.2017.02171

Received: 21 October 2017; Accepted: 11 December 2017;
Published: 22 December 2017.

Edited by:

José Manuel Pérez-Pérez, Universidad Miguel Hernández de Elche, Spain

Reviewed by:

Gabriela Carolina Pagnussat, National University of Mar del Plata, Argentina
Daisuke Maruyama, Yokohama City University, Japan

Copyright © 2017 Lu, Yu, Tian, Huang, Tan, Xie, Hao, Li, Luan and Chen. 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) or licensor 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: Dongping Li, dli@hunnu.edu.cn Sheng Luan, sluan@berkeley.edu Liangbi Chen, chenliangbi@126.com

These authors have contributed equally to this work.