Regulation of Plant Growth and Development: A Review From a Chromatin Remodeling Perspective

In eukaryotes, genetic material is packaged into a dynamic but stable nucleoprotein structure called chromatin. Post-translational modification of chromatin domains affects the expression of underlying genes and subsequently the identity of cells by conveying epigenetic information from mother to daughter cells. SWI/SNF chromatin remodelers are ATP-dependent complexes that modulate core histone protein polypeptides, incorporate variant histone species and modify nucleotides in DNA strands within the nucleosome. The present review discusses the SWI/SNF chromatin remodeler family, its classification and recent advancements. We also address the involvement of SWI/SNF remodelers in regulating vital plant growth and development processes such as meristem establishment and maintenance, cell differentiation, organ initiation, flower morphogenesis and flowering time regulation. Moreover, the role of chromatin remodelers in key phytohormone signaling pathways is also reviewed. The information provided in this review may prompt further debate and investigations aimed at understanding plant-specific epigenetic regulation mediated by chromatin remodeling under continuously varying plant growth conditions and global climate change.


INTRODUCTION
The packaging of genetic material into nucleosomes is a distinctive evolutionary feature of eukaryotic cells. Nucleosomes are repetitive units consisting of 147 bp DNA strands tightly wrapped around a central octamer comprising one histone heterotetramer (H3/H4) and two histone heterodimers (H2A/H2B). Histones are highly conserved proteins found in all eukaryotes as core nucleosome units (Suzuki and Bird, 2008). Together, the histone octamer and DNA resemble "beads" on a string and are referred to as chromatin (Luger et al., 1997). This packaging ensures that long DNA strands are tightly condensed by supercoiling to precisely fit into the nucleus. Such compaction of nucleosomes in chromatin hinders DNA accessibility to important regulatory proteins essential for various nuclear processes. However, cells have evolved in response to this impediment through chromatin remodeling (Groth et al., 2007).
Gene regulatory mechanisms in eukaryotic cells (such as transcription, DNA repair and replication) act upon chromatin structure as a substrate. These activities induce cellular changes and regulate gene expression in a number of biological processes, including genome stability, recombination, developmental reprogramming and response to extracellular signals (Feng et al., 2010;Soria et al., 2012;Zhu et al., 2013). The regulatory precision of these fundamental genome processes relies on the high fidelity of chromatin remodeling mechanisms that permit temporal access to -or blocking of -vital DNA sequences, such as gene promoters. Histone modifications, nucleosome remodeling and DNA methylation have been shown to regulate chromatin structure and gene expression (Henikoff and Shilatifard, 2011).
There are two main players regulating chromatin dynamics: (1) chromatin remodelers that alter DNA-histone interactions by energy harnessed through ATP hydrolysis and (2) nucleosome-modifying enzymes that modulate DNA and histone residues by specifically adding or removing covalent modifications (Jerzmanowski, 2007). Organisms rely on gene expression regulation to achieve normal cell differentiation, organogenesis, growth and development. Moreover, gene expression regulation is temporally and spatially coordinated via crosstalk between chromatin remodeling complexes (CRCs) and the transcription machinery (Deem et al., 2012). In plants, such precise control of gene expression mediated by chromatin modifications in response to endogenous and environmental stimuli is fundamental for proper development and reproductive success (Sarnowski et al., 2005;Bezhani et al., 2007;Han et al., 2012;Archacki et al., 2013;Efroni et al., 2013;Sarnowska et al., 2013;Qin et al., 2014;Vercruyssen et al., 2014).
Plant development can be divided into the embryonic and postembryonic phases. The embryonic development phase includes the establishment of the seedling apical-basal axis, the shoot apical meristem (SAM) and the root apical meristem (RAM). The subsequent establishment of the leaf, stem and flower meristems occurs in the postembryonic phase. In this review, we discuss recent investigations underpinning the involvement of SWI/SNF chromatin remodeling ATPases in regulating key plant growth and development processes, including meristem establishment and maintenance, cell differentiation, organ initiation, flower morphogenesis and flowering time regulation. We also discuss the role of chromatin remodelers in the plant response to key phytohormone signals. This overview may be useful for framing the current knowledge gaps, thereby stimulating further debate and research aimed at a comprehensive understanding of epigenetic regulatory mechanisms in plant development. This in turn may guide molecularbased plant improvement techniques for desirable agronomic traits.

CLASSIFICATION OF EUKARYOTIC CHROMATIN REMODELING COMPLEXES
Chromatin remodeling complexes are evolutionarily conserved multi-unit protein complexes that regulate chromatin structure by altering nucleosome composition and interactions (Narlikar et al., 2002). A common feature of all purified CRCs is that they harbor an ATPase/helicase of the SWITCHING DEFECTIVE2/SUCROSE NON-FERMENTING2 (SWI2/SNF2) family as their catalytic core. The SWI/SNF family is part of superfamily2 (SF2), a large family of helicases and translocases, and is named after the first identified CRC (Peterson et al., 1994). SWI/SNF CRCs utilize the energy derived from ATP hydrolysis to control accessibility to vital DNA sequences by influencing nucleosome structure and position and determining the kind of variant histone subspecies to be incorporated (Eisen et al., 1995;Clapier and Cairns, 2009).

SWI/SNF Subfamily Remodelers
The SWI/SNF subfamily of remodelers initially purified from Saccharomyces cerevisiae is probably the most comprehensively studied. SWI/SNF subfamily CRCs have a well-established role in gene expression regulation. The SWI/SNF subfamily remodelers contain 8-14 subunits, and the catalytic ATPases of most SWI/SNF subfamily remodelers are composed of a helicase-SANT domain, a post-HSA domain and a C-terminal bromodomain. While the fungal SWI/SNF subfamily ATPases consist of a pair of actin-related proteins (ARPs) (Cairns et al., 1998), higher orthologs of SWI/SNF subfamily complexes contain a dimer of an ARP and actin (Lessard et al., 2007). The mode of action of SWI/SNF complexes has been characterized as sliding and/or ejecting nucleosomes at many target loci, but they reportedly have no vital role in the assembly of eukaryotic chromatin structure (Clapier and Cairns, 2009). It was recently reported that the Arabidopsis SWI/SNF complex expedites its role in activating and repressing target gene expression by binding to both promoters and terminators and that it regulates the expression of both promoter-centered genes and non-coding RNAs (Archacki et al., 2017).

Imitation Switch (ISWI) Subfamily Remodelers
The ISWI subfamily remodelers have 2-4 subunits. Eukaryotic ISWI remodeler complexes typically have 1 or 2 distinct catalytic subunits and specialized attendant proteins that give rise to various domains. These domains include plant homeodomains, bromodomains, DNA-binding histone fold motifs and additional DNA-binding motifs (Clapier and Cairns, 2009). ISWI complexes were initially purified from Drosophila melanogaster. They include the nucleosome remodeling factor (dNURF), chromatin accessibility complex (dCHRAC) and ATP-utilizing chromatin assembly and remodeling factor (dACF) (Corona and Tamkun, 2004). SANT-like ISWI ATPases contain a SANT domain adjacent to a SLIDE domain in their C-terminus, which acts as a binding site for unmodified histone tails and DNA. The diversity resulting from attendant subunits is exhibited in the modes of action of the ISWI family complexes. Both ACF and CHRAC have been shown to promote chromatin assembly and transcription repression through the optimization of nucleosome spacing, whereas NURF assists RNA polymerase II (RNAPII) activation by randomizing nucleosome spacing (Corona and Tamkun, 2004).

Chromodomain Helicase DNA-Binding (CHD) Subfamily Remodelers
The CHD subfamily remodelers were first purified from Xenopus laevis and comprise 1-10 subunits. The N-terminus of their catalytic subunit consists of two chromodomains arranged tandemly, with the composition varying from monomeric in lower eukaryotes to multimeric in vertebrates (Marfella and Imbalzano, 2007). CHD subfamily remodelers vary in their structure, composition and function, due in part to the diversity of their chromodomains. One of the members of the CHD subfamily in vertebrates, the nucleosome remodeling and deacetylase (Mi-2/NuRD) complex, has repressive roles due to its inclusion of histone deacetylases (HDAC1/2) and methyl CpG-binding domain (MBD) proteins. In contrast, other CHD subfamily remodelers have been reported to promote transcription by either ejecting or sliding nucleosomes along the DNA double strand (Denslow and Wade, 2007).

Inositol Requiring 80 (INO80) Subfamily Remodelers
The INO80 subfamily is the most recently characterized chromatin remodeler subfamily. Many INO80 subunit homologs have been identified in yeast, fruit fly, mammals and plants, making it the most conserved subfamily. The presence of a split ATPase subunit distinguishes INO80 complexes from the SWI/SNF, CHD and ISWI subfamilies (Morrison and Shen, 2009). In S. cerevisiae, the INO80 subfamily is represented by two complexes, INO80 and Swi2/snf2-related 1 (SWR1); in mammals, it is represented by three complexes, INO80, Snf2-related CBP activator protein (SRCAP) and p400. D. melanogaster has INO80 and p400 complexes (Morrison and Shen, 2009;Bao and Shen, 2011). S. cerevisiae INO80 and SWR1 ATPases are approximately 1.2-1.5 MDa in mass and are reported to contain 15 and 14 subunits, respectively (Shen et al., 2000;Krogan et al., 2003;Mizuguchi et al., 2004). In general, the INO80 subfamily has a relatively conserved composition of individual complexes and a high degree of homology in the ATPase subunit. Studies of the S. cerevisiae SWR1 complex indicate the importance of a spacer (split) region in the ATPase subunit, as deletion of this region leads to dissociation of a number of subunits from the complex, including the RuvB-like Rvb1 and Rvb2 subunits (Wu et al., 2005). The INO80 subfamily is responsible for various functions in eukaryotic cells including transcriptional activation and DNA double-strand break (DSB) repair (Ebbert et al., 1999).

INVOLVEMENT OF SWI/SNF ATPases IN MERISTEM ESTABLISHMENT AND MAINTENANCE
Plant development is characterized by the presence of stem cells with the capacity to self-renew and transform into tissuespecific founder cells. The stem cells of the RAM and SAM have been widely studied in plants and are found at the root and shoot tips, respectively (Shen and Xu, 2009). Stem cell homeostasis and identity in both plants and mammals are associated with the activity of SWI/SNF chromatin remodeling ATPases (Ori et al., 2000;Kwon et al., 2005;Ho et al., 2009;Aichinger et al., 2011). Perturbations in the Polycomb group (PcG) repressive complex, histone acetylation or chromatin assembly may lead to improper RAM or SAM development (Phelps-Durr et al., 2005;Schubert et al., 2006;Barrero et al., 2007;Xu and Shen, 2008;Kornet and Scheres, 2009). Individual Arabidopsis SWI/SNF subfamily chromatin remodelers (BRM, SYD, CHR12 and CHR23) (Flaus et al., 2006) are also involved in regulating numerous plant developmental processes (Farrona et al., 2004;Hurtado et al., 2006;Kwon et al., 2006;Bezhani et al., 2007;Tang et al., 2008;Wu et al., 2012). SYD promotes SAM maintenance by binding to the promoter region of its target gene WUSCHEL (WUS) and activating WUS expression in the organizing center (OC) region of the SAM (Figure 1). Consistent with this function, Arabidopsis syd mutant plants exhibit reduced WUS transcript levels accompanied by abnormal SAM development (Kwon et al., 2005).
The CHR12 and CHR23 ATPases have redundant roles in plant development processes including meristem initiation and maintenance. Plants with strong double mutant chr12chr23 combinations show embryonic lethality, endosperm defects and failure to initiate stem cell populations in both roots and shoots, whereas plants with weak double mutant chr12chr23 combinations are small viable plants with noticeable defects in RAM and SAM maintenance .
A study by Wu et al. (2015) demonstrated a role of chromatin in local developmental progressions in the root and shoot. In the SAM, cells with high auxin levels initiate proteolysis of Aux/IAA leading to the dissociation of the corepressor complex TOPLESS-HISTONE DEACETYLASE 19 FIGURE 1 | Chromatin remodelers in shoot and root apical meristem establishment and maintenance. SYD binds to the promoter region of WUS in the OC region of the SAM, activating WUS expression to promote SAM maintenance. CHR12 and CHR23 have redundant roles in plant development regulation, as single mutations in either produce no obvious defects but strong double mutations lead to impaired SAM maintenance. BRM acts in the PLT pathway to regulate the expression of PIN genes, which in turn influence auxin distribution in the QC region to ensure RAM maintenance.
(TPL-HDA19). This enables the recruitment of SYD and BRM to direct the acquisition of flower primordium founder cell fate . In the RAM, a small group of mitotically inactive cells known as the quiescent center (QC) maintains the root stem cells. BRM was found to act in the PLETHORA (PLT) pathway to maintain the root stem cell niche by altering the expression of PIN-FORMED (PIN) genes responsible for auxin distribution in the RAM, as illustrated in Figure 1. brm mutants exhibit faulty root stem cell niche maintenance, reduced meristem activity and retarded root growth .
To attain continuous plant growth, cells derived from pluripotent stem cells must undergo asymmetric cell division and expansion. This allows for the generation of lateral organs and the maintenance of stem cell populations for additional growth (Jarillo et al., 2009). The role of BRM in ensuring asymmetric cell division and cell fate determination in both plant and animal stem cells was discussed extensively in a recent review (Pillitteri et al., 2016).
Our current knowledge of mechanisms involving chromatinmediated regulation of plant stem cell initiation and maintenance remains limited to the few Arabidopsis SWI/SNF complexes discussed above. However, emerging evidence suggests complex interconnections among many players including key hormone signaling pathways. This underscores the ability of plants to activate or arrest lateral organ founder cell formation in response to both internal developmental signals and external biotic and abiotic stress signals. These attributes may eventually be harnessed or targeted for crop improvement applications.

CHROMATIN REMODELING IN CELL DIFFERENTIATION, ORGAN INITIATION AND DEVELOPMENT
Stem cells in the SAM initiate organ founder cells that later differentiate into aboveground organ-specific tissues such as leaves and stems (Sinha, 1999;Laux, 2003). Plant roots are formed from a reservoir of undifferentiated cells in the RAM called the root stem cells. Mature plant organs usually maintain relatively undifferentiated cells as a fallback for hormonal stimuli or mechanical injury, helping to generate new tissues and organs through cellular reprogramming (Ikeuchi et al., 2015). Cellular differentiation results from global changes in gene expression patterns and these changes involve many transcription regulators and are epigenetically mediated by chromatin remodeling (Bruex et al., 2012;Taylor-Teeples et al., 2015). ANGUSTIFOLIA3 (AN3)/GRF-INTERACTING FACTOR1 (GIF1), a member of the GIF family of transcriptional coactivators, plays a key role in Arabidopsis shoot development (Kim and Kende, 2004), cotyledon identity establishment during embryogenesis (Kanei et al., 2012) and leaf size increase resulting from increased cell number (Horiguchi et al., 2005;Lee et al., 2009). Transcriptional coactivators often work together with DNA-binding transcription factors to promote transcription either by recruiting chromatin remodelers or stimulating general complex formation around RNA polymerase II (Pol II). Genetic interaction between AN3 and the Arabidopsis SWI/SNF chromatin remodeling complex BRM (Figure 2) suggests that AN3 recruits SWI/SNF complexes to promote cell division during leaf development (Vercruyssen et al., 2014). BRM is recruited to its target gene loci via association with the plant-specific H3K27 demethylase RELATIVE OF EARLY FLOWERING 6 (REF6). Through its zinc-finger (ZnF) domains, REF6 recognizes genomic loci harboring a CTCTGYTY motif . A forward genetic screen in Arabidopsis indicated that BRM and SWINGER (SWN) (a key component of Polycomb Group Repressive Complex 2 in plants) antagonistically control vegetative phase change through the temporal expression of miR156 at the nucleosome level. Specifically, the accelerated vegetative phase change of brm mutants was accompanied by reduced miR156 expression and increased levels of H3K27me3 at the MIR156A locus (Xu et al., 2016).
A study of the chromatin remodeler protein ZmCHB101, which is the core subunit of maize SWI3, revealed its key roles in normal maize growth and development. ZmCHB101 controls the transcriptional reprogramming of a set of genes involved in gene expression regulation, photosynthesis, metabolic regulation and stress response. The RNAi maize lines generated in the study exhibited improper tassel and cob development and abaxially curling leaves caused by increased bulliform cell numbers (Yu et al., 2016).
Chlorophyll biosynthesis is a critical mark of the transition from heterotrophic to autotrophic growth in plants. Physical interaction between BRM and the transcription factor PHYTOCHROME-INTERACTING FACTOR 1 (PIF1) was shown to regulate chlorophyll biosynthesis in Arabidopsis (Figure 2). When exposed to light, dark-grown brm plants exhibit higher greening rates, reduced protochlorophyllide accumulation and lower levels of reactive oxygen species (ROS) compared to wild-type plants; there is also increased expression of NADPH:protochlorophyllide oxidoreductase A (PORA), PORB and PORC, enzymes which accelerate a key step in chlorophyll biosynthesis .
The importance of chromatin remodelers for proper plant growth progression and development is exemplified by their involvement in asymmetric cell differentiation and in initiating organ founder cells. Proper plant growth also involves precise developmental phase transitions, and the antagonism between SWI/SNF ATPases and PcG repressive complex components is crucial for these shifts.

CHROMATIN REMODELER-MEDIATED FLOWERING AND FLOWER MORPHOGENESIS
The precise regulation of the transition from vegetative growth to flowering is paramount for plant reproductive success. This process is characterized by the transition of the vegetative SAM into an inflorescence meristem (IM) and the initiation of floral meristems (FMs) (Sablowski, 2007;Kaufmann et al., 2010). While SAM maintenance ensures indeterminate plant growth, the determinate nature of FMs determines reproductive success, seed development and the yield of agricultural crops (Liu et al., 2011). Complex regulatory networks of transcription factors and chromatin remodelers guide flowering time and flower development while integrating both internal and external signals (Wils and Kaufmann, 2017). These networks comprise photoperiod, vernalization and thermo-sensory pathways for sensing long days, cold winter and ambient temperature, respectively, together with pathways responsive to internal factors, such as the age pathway and the gibberellins (GA) signaling pathway (He, 2012).
In Arabidopsis, a repressor complex that consists of the two MADS box transcription factors MADS AFFECTING FLOWERING 4/5 (MAF4/5), FLOWERING LOCUS C (FLC) and SHORT VEGETATIVE PHASE (SVP) serves as a negative regulator of flowering time. The components directly repress the expression of the floral pathway integrators FLOWERING LOCUS T (FT) and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1) Li et al., 2008;He, 2012). FRIGIDA (FRI) promotes higher FLC levels that inhibit flowering (Michaels and Amasino, 2001) through the recruitment of multiple active chromatin modifications at the FLC locus (Choi et al., 2011). Vernalization overrides the FRI-mediated activation of FLC expression and thereby enables flowering Crevilleńn and Dean, 2011).
The core subunit components of the Arabidopsis SWR1 chromatin remodeling complex (including PHOTOPERIOD-INDEPENDENT EARLY FLOWERING 1 (PIE1), ACTIN RELATED PROTEIN 6 (ARP6) and SWR1 COMPLEX 6 (SWC6)/SERRATED LEAVES AND EARLY FLOWERING (SEF)) have been shown to play important roles in regulating the proper growth and development of most plant organs. Importantly, SWR1 controls plant development by generating a balance between microRNAs and target mRNAs at the transcriptional level (Choi et al., 2016). It was recently demonstrated that SWR1 regulates gene expression by establishing lowly accessible and highly accessible nucleosome structure at the first nucleosome upstream and downstream of the transcription start site (TSS), respectively (Dai et al., 2017). SWR1 subunit loss-offunction mutants exhibit pleiotropic phenotypes including early flowering, serrated leaves, frequent absence of inflorescence internodes, bushy growth and flowers with altered organ number and size (Choi et al., 2005;Deal et al., 2005;Martin-Trillo et al., 2006;March-Diaz et al., 2007;Qin et al., 2014). H2A.Z deposition around the FLC TSS by SWR1 is necessary for FRI-meditated activation of FLC (Figure 3). One line of evidence is that functional disruption of SWR1 prevents H2A.Z deposition at FLC chromatin, suppressing its expression and leading to early flowering (Choi et al., 2007;Deal et al., 2007). Additionally, PIE1 mutations were earlier shown to substantially reduce FLC transcript levels, with a concomitant conversion of the winter-annual habit to the rapid flowering summer-annual habit (Noh and Amasino, 2003). A recent study revealed an Arabidopsis homolog of the yeast SANT domain protein Swc4/Eaf2 as a novel SWR1-C subunit. SWC4 is a DNA-binding protein that contributes to the recruitment SWR1-C through specific recognition of AT-rich DNA segments in chromatin regions of target genes to deposit H2A.Z. Further, knock-out and knockdown studies showed that SWC4 is essential for both embryo viability and the control of postembryonic processes, including flowering time, by repressing transcription of a number of genes including the floral integrator FT and key transcription factors (Gomez-Zambrano et al., 2018).
The AtINO80 complex is required for somatic homologous recombination (HR) and expression regulation of FLC and MAF4/5 by facilitating the enrichment of H2A.Z at their ends. Independent Atino80-5 and Atino80-6 mutant alleles display similar pleiotropic phenotypes of small plant size, reduced organ size and late flowering. These observations provide a link between plant responses to environmental and developmental signals and epigenetic mechanisms involved in plant chromatin stability (Zhang et al., 2015).
The SWP73B (BAF60) subunit of the Arabidopsis SWI/SNF complex has also been implicated in flowering time control through its involvement in chromatin loop formation at the FLC locus (Jegu et al., 2014). SWP73A has been shown to be confined to flowering time modulation under short day conditions, with functional overlap between SWP73A and SWP73B during embryogenesis (Sacharowski et al., 2015).
SVP, another key flowering repressor, is highly expressed during the vegetative phase to promote growth (Hartmann et al., 2000) but is down-regulated during the floral transition by the autonomous and GA signaling pathways (Li et al., 2008). FT and SOC1 are subsequently activated to promote flowering (Figure 3). One study proposed that BRM controls flowering time in Arabidopsis by directly activating SVP expression . Genome-wide analysis of H3K27me3, a histone mark associated with gene repression, in brm mutant seedlings revealed increased H3K27me3 deposition at several genes including SVP, indicating an antagonism between BRM and PcG repressor proteins .
Another key flowering time regulator in Arabidopsis activated by CONSTANS (CO) under long days to induce flowering is the FT-encoded florigen protein (FT) (Corbesier et al., 2007). FT moves from the phloem to the SAM and forms a complex with the bZIP transcription factor FD to activate the expression of the FM identity genes LEAFY (LFY) and APETALA1 (AP1). This activation leads to the formation of the floral primordium, which sequentially generates three types of lateral floral organs (sepals, petals and stamens) (Zik and Irish, 2003;Abe et al., 2005;Wigge et al., 2005). LFY recruits SYD and BRM ATPases to induce the expression of the floral homeotic regulator AGAMOUS (AG) by removing H3K27me3 marks on its second intron (Figure 3) . The SWR1 complex is also involved in FT expression regulation, with functional disruption of SWR1 leading to temperatureinsensitive FT activation and early flowering. An ambient temperature increase from 17 to 27 • C causes eviction of the H2A.Z nucleosomes, which enables FT transcription by Pol II (Kumar and Wigge, 2010).
Studies of the CHD3 chromatin remodeler PICKLE (PKL) have highlighted its role in plant reproductive development by promoting crosstalk between the sporophytic and gametophytic generations. Loss of PKL in the maternal sporophyte leads to improper development of the Arabidopsis female gametophyte, integument and pollen tube, accompanied by delayed ovule and embryo development (Carter et al., 2016).
It was recently shown that during megasporogenesis, somatic cells cooperatively use SWR1 to restrict female reproductive founder cell specification to a single cell in the ovule primordia by incorporating H2A.Z at a particular WRKY28 nucleosome and promoting expression of the gene (Zhao et al., 2018). The WRKY28 transcription factor is exclusively expressed in hypodermal somatic cells surrounding the megasporocyte and represses those cells from differentiating into functional megasporocytes (Zhao et al., 2018). Other separate findings demonstrated that both BRM and SWR1 are involved in determining inflorescence architecture in response to developmental cues Cai et al., 2017).
The above findings reveal mechanisms involving the recruitment of SWI/SNF ATPases to specific flower development regulatory pathways at an appropriate time. They also emphasize the centrality of SWI/SNF complexes in shaping plant growth and ensuring the continuity of plant viability through generations by precise spatiotemporal control of the relevant developmental processes. Nevertheless, these conclusions about important regulatory mechanisms are generally based on findings from model plants such as Arabidopsis. Thus, the understanding of such regulatory mechanisms in agriculturally important crop species remains inadequate and will require further investigation.

CHROMATIN REMODELERS IN PHYTOHORMONE SIGNALING PATHWAYS
Plant hormones are critical for the proper regulation of plant growth and development processes including seed germination, vegetative and reproductive growth and abiotic stress response. The biosynthesis and degradation of plant hormones are also tightly controlled through the transcriptional regulation of target genes. SWI/SNF ATPases are involved in plant hormone responses through physical interaction with hormone signaling pathway components and transcriptional regulators of genes involved in hormone biosynthesis and perception (Sarnowska et al., 2016).
Abscisic acid (ABA) is an important phytohormone that promotes seed dormancy and arrests growth in postgermination embryos under water stress conditions. In the absence of stress stimuli, BRM was initially implicated in repressing the activity of the ABA pathway, with adult brm mutants exhibiting increased drought tolerance . It was later revealed that important ABA signaling pathway components physically interact with BRM, leading to post-translational phosphorylation/dephosphorylation of BRM. For example, phosphorylation of BRM by SnRK2 kinases leads to its inhibition, while PP2CA-mediated dephosphorylation restores the ability of BRM to repress the ABA response (Figure 4). Moreover, the phosphomimetic BRM mutant shows hypersensitivity to ABA (Peirats-Llobet et al., 2016).
BRM has also been shown to play a direct role in the positive regulation of GA biosynthesis by binding to chromatin near the GA3ox1 promoter, thereby activating the gene (Figure 4). Arabidopsis brm null mutants exhibit a significant decrease in active GA levels (Archacki et al., 2013). Furthermore, transcriptional profiling revealed that most genes involved in the GA and auxin signaling pathways are affected in both syd and brm null mutants (Bezhani et al., 2007). Previous studies showed that plants over-expressing CHR12 had enhanced growth arrest when exposed to drought or heat stress (Mlynarova et al., 2007). In addition, SYD was linked to ethylene (ET)-and jasmonic acid (JA)-dependent gene regulation (Walley et al., 2008), and the SWI3B subunit was found to interact with a negative regulator of ABA signaling, the PP2C-type phosphatase HAB1 (Saez et al., 2008).
During development, plants transition from the embryonic stage to the seedling stage. Previous studies have characterized the joint effects of PKL and GA in repressing embryonic traits during plant development transitions (Zhang et al., 2008;Zhang et al., 2012). Specifically, PKL expression represses the embryonic state by controlling a significant number of GA-responsive genes. pkl seedlings exhibit a semi-dwarf phenotype similar to that of GA-response mutants and are able to express embryonic traits under GA-biosynthesis inhibition. In contrast, treatment of pkl mutants with GA greatly decreases their characteristic pickleroot phenotype (Henderson et al., 2004). Both PKL and BRM CRCs have been proposed to act as positive regulators of the GA pathway possibly through distinct mechanisms. Unlike brm mutants, pkl mutant plants have an increased abundance of active GA (Archacki et al., 2013). Recently, PKL was found to positively regulate most GA-mediated developmental processes including promoting vegetative growth (hypocotyl, leaf, and inflorescence stem elongation) and phase transitions (i.e., the juvenile-toadult and vegetative-to-reproductive transitions) (Park et al., 2017).
Excess cytokinin (CK) production inhibits primary root elongation and weakens lateral root development (Kuderova et al., 2008). SWP73B is one of the accessory subunits of Arabidopsis SWI/SNF complexes shown to positively regulate root development and cell cycle progression in the root meristem by suppressing CK biosynthesis (Figure 4). SWP73B negatively regulates the CK biosynthesis genes ADENOSINE PHOSPHATE-ISOPENTENYLTRANSFERASE (IPT3) and (IPT7) and the CKregulated cell cycle inhibitor KIP-RELATED PROTEIN7 (KRP7) by hindering the deposition of active histone marks on their gene bodies (Jegu et al., 2015).
In aggregate, these findings indicate that both phytohormone biosynthesis and degradation in response to extracellular and intracellular cues partly depend on SWI/SNF chromatin remodeling ATPases. The findings also suggest the role of SWI/SNF ATPases as a hub in plant perception and response to phytohormone signaling as well as hormone crosstalk through direct physical interactions with hormone signaling pathway components. The outcomes of these interactions influence the plant response to abiotic stress, enabling plant adaptability under changing climates.

CONCLUDING REMARKS AND FUTURE PERSPECTIVES
Chromatin remodeling has been extensively studied in the context of various regulatory and developmental processes in a number of eukaryotic organisms, including humans, mice, yeast, fruit fly and Arabidopsis. Phylogenetic analysis suggests that the chromatin remodeling machinery and their modes of operation are evolutionarily conserved across eukaryotes. However, SWI/SNF subunit loss-of-function studies have uncovered varied organism-specific phenotypes. These phenotypes also depend on the strength of a given mutation, leading to phenotypic differences among single and double mutants of SWI/SNF subunit genes. The functional redundancy of some SWI/SNF complex subunits also necessitates further in-depth analyses of their interaction patterns in different plant development pathways.
As discussed above, a number of plant regulatory and developmental transitions are controlled by chromatin modifiers through complex pathways in response to both endogenous and environmental factors. These precisely orchestrated mechanisms are heritable, underscoring their importance for plant survival in changing habitats. Moreover, the dynamics of these epigenetic controls go hand in hand with changes in plant growth conditions. Positive attributes that could potentially be integrated into plant breeding schemes are of interest to many plant scientists and breeders insofar as they may yield varieties that can withstand adverse weather conditions, early flowering or various biotic stresses and maximize nutrient utilization for improved yield. High-throughput technologies together with the vast genomic data presently available in public repositories should facilitate comparative and functional studies aimed at plant improvement. Future studies in other species of interest (e.g., rice and other crops) will likely build upon the findings on ATP-dependent CRCs in Arabidopsis and more recently in maize. Plant-specific molecular and genetic approaches should also characterize regulatory differences between developmental stages and under different growth conditions for a more comprehensive understanding of the involvement of SWI/SNF chromatin modifiers in plant growth and development.

GENERAL OUTLOOK
The following research questions and topics are of particular interest in terms of how CRCs may be involved in various processes either directly or indirectly related to plant development.
(1) Involvement of SWI/SNF ATPases in flowering regulation in the temperate legume model plant Medicago truncatula, whose flowering is prompted by winter cold and long-day photoperiods despite the absence of an FLC gene.
(2) The role played by chromatin remodelers in oxidative stress remediation processes resulting from various metabolic activities in plant cells other than DNA double-strand break repair.
(3) Besides their known function in the phosphate starvation response, there is a need to ascertain other roles of SWI/SNF remodelers in mediating the uptake of essential micro-and macronutrients from the soil in conjunction with nutrient transporter gene families and rhizosphere microbial activities. (4) The mechanism by which the chromatin remodeling complex SWR1 mediates chromatin structural dynamics by replacing the core H2A-H2B histone dimer with the H2A.Z-H2B dimer in octamers is well characterized. However, the molecular mechanisms underlying the reverse process remain elusive. (5) The specific roles of accessory subunits of Arabidopsis SWI/SNF CRCs in regulating plant development are only beginning to be understood. The latest example is SWP73 involvement in the cell cycle, leaf development, flowering time and embryogenesis. Much remains to be uncovered in this regard.

AUTHOR CONTRIBUTIONS
SO and SC conceived the idea, wrote the manuscript, and drafted the figures. SP designed and organized figures and revised the manuscript. WL, MY, MA, and HZ revised the manuscript and organized the figures. YQ conceived the idea and revised and organized the manuscript.

FUNDING
This work was supported by NSFC (31761130074, U1605212, and 31470284) and a Newton Advanced Fellowship to YQ.

ACKNOWLEDGMENTS
We extend our apologies to all our colleagues whose work could not be reviewed here owing to space limitations. We are indebted to Fujian Agriculture and Forestry University for its financial support and to members of the Qin Lab (Haixia Institute of Science and Technology, Centre for Genomics and Biotechnology) for their motivation and suggestions for this manuscript.