Sec. Plant Genetics and Genomics
Volume 6 - 2015 | https://doi.org/10.3389/fpls.2015.00207
Genetic control of flowering time in legumes
- School of Biological Sciences, University of Tasmania, Hobart, TAS, Australia
The timing of flowering, and in particular the degree to which it is responsive to the environment, is a key factor in the adaptation of a given species to various eco-geographic locations and agricultural practices. Flowering time variation has been documented in many crop legumes, and selection for specific variants has permitted significant expansion and improvement in cultivation, from prehistoric times to the present day. Recent advances in legume genomics have accelerated the process of gene identification and functional analysis, and opened up new prospects for a molecular understanding of flowering time adaptation in this important crop group. Within the legumes, two species have been prominent in flowering time studies; the vernalization-responsive long-day species pea (Pisum sativum) and the warm-season short-day plant soybean (Glycine max). Analysis of flowering in these species is now being complemented by reverse genetics capabilities in the model legumes Medicago truncatula and Lotus japonicus, and the emergence of genome-scale resources in a range of other legumes. This review will outline the insights gained from detailed forward genetic analysis of flowering time in pea and soybean, highlighting the importance of light perception, the circadian clock and the FT family of flowering integrators. It discusses the current state of knowledge on genetic mechanisms for photoperiod and vernalization response, and concludes with a broader discussion of flowering time adaptation across legumes generally.
Many aspects of plant growth and development are highly attuned to the environment, and this is particularly true of the transition from vegetative growth to the flowering state. Genetic variation that affects the timing of flowering and its regulation by environmental factors has clear significance for the performance of crop species. Many species have a requirement for exposure to specific photoperiods and/or temperatures in order to flower, and flowering may be significantly delayed or prevented if these requirements are not met. Genetic changes that relax or eliminate these constraints have enabled expansion to a wider latitudinal and climatic range and allowed greater flexibility in seasonal cropping practices. Conversely, delayed flowering may be an advantage in other situations, as it may reduce damage from certain abiotic stresses and lead to greater yield through increased biomass accumulation prior to flowering. Knowledge of how individual genetic variants combine to provide adaptation in specific situations can be valuable for breeding purposes, as it can accelerate introgression of new traits into adapted backgrounds and may allow the directed modification of phenology for specific target environments.
The major crop legumes fall within two sister clades that are included in the larger group of papilionoid legumes, often referred to as the galegoid and phaseoloid clades (Cronk et al., 2006). In general, species within the galegoid clade (e.g., pea, lentil, chickpea, faba bean) are from temperate regions and with respect to flowering time control are vernalization-responsive long-day plants (LDPs), whereas those in the phaseoloid clade (e.g., soybean, cowpea, pigeonpea, common bean) generally originate from lower latitudes and are short-day plants (SDPs; Summerfield and Roberts, 1985b). Two other important crop legumes, peanut (Arachis hypogaea) and lupin (Lupinus spp.) are basal to both of these clades. Not surprisingly, in view of their respective origins at low and high latitudes, peanut has characteristics of a SDP (Bagnall and King, 1991) and the commonly grown lupin species are vernalization-reponsive LDP (Summerfield and Roberts, 1985c).
While the defining feature of the vegetative-to-reproductive transition is the conversion of meristems to produce flowers rather than vegetative shoots, in a natural environment this is also accompanied by significant changes to a wide range of other developmental traits, including stem elongation, apical dominance, lateral branching, resource allocation, maturity and yield. In some species, genes and environmental factors that affect the initial flowering transition can also continue to have a significant influence on post-flowering processes affecting fertility and pod development. Thus, although flowering time can be seen from one perspective as a relatively simple trait, in reality it is linked to fundamental decisions made by the plant about when and how to allocate resources, and thus participates in a complex network of two-way interactions with other developmental processes.
Over recent years there has been a dramatic increase in the number of legume species with genome sequences and/or significant genomic resources (Young and Bharti, 2012). However, in the study of flowering time, as for other developmental processes, no one legume species has emerged as the predominant model. Most work on flowering time has focused on the two species pea (Pisum sativum) and soybean (Glycine max), which respectively represent the temperate LDP and warm-season SDP. This is partly due to the long history in the use of both of these species for flowering research and the accumulation of knowledge on its genetic control (Murfet, 1985; Summerfield and Roberts, 1985a; Weller et al., 1997b, 2009; Watanabe et al., 2012). Interestingly, the two legume model species Medicago truncatula (barrel medic) and Lotus japonicus, which have been prominent in studies of nitrogen fixation and other fundamental processes, and have genome sequences available, have so far not been deeply exploited for investigation of flowering time control.
The availability of extensive genomic resources for several legume species and well-documented synteny has enabled a comprehensive inventory of genes potentially relevant for flowering time control. This has been useful both in identification of candidate genes for flowering loci, and in exploring the molecular physiology of flowering through gene expression studies and reverse genetics. It has also dramatically improved the prospects for discovering legume-specific genes through purely positional approaches. Well over 100 genes that contribute to control of flowering time have been identified in Arabidopsis and rice, and the functions and interactions of these genes are regularly reviewed (e.g., Kim et al., 2009; Amasino and Michaels, 2010; Andres and Coupland, 2012; Pin and Nilsson, 2012; Brambilla and Fornara, 2013; Song et al., 2013). In legumes, several compendia of flowering gene homologs are already available (Hecht et al., 2005; Kim et al., 2012; Watanabe et al., 2012). While the basic genes and gene families central to pathways controlling flowering time in Arabidopsis appear to be largely conserved in legumes, there are numerous examples of gene duplication and loss. This is likely to reflect the history and consequences of genome duplications after the divergence of the Arabidopsis and legume lineages (Young and Bharti, 2012).
Photoreceptors provide primary information about the light environment that enables detection of daylength. Legumes have a standard complement of only three phytochromes (phyA, phyB, and phyE; Hecht et al., 2005), and lack a representative of the ancient phyC clade, although the phyA lineage has undergone a more recent duplication in the phasioloid legumes (Liu et al., 2008). The cryptochrome gene CRY1 has also been duplicated in the phasioloid legumes, while an older duplication of the CRY2 gene is common to all legumes (Platten et al., 2005b). In contrast, only two LOV-domain flavoprotein photoreceptors in the FKF1/ZTL family are present in legumes. The circadian clock is also important for photoperiod measurement, and while all major Arabidopsis clock genes are represented, the galegoid legumes appear to have only a single gene orthologous to the circadian-clock related MYB transcription factor genes CCA1 and LHY (Hecht et al., 2007), whereas the TOC1, GI, and ELF3 genes have variously undergone duplication in the two legume groups. The CONSTANS protein, which integrates light and circadian signaling for photoperiod-specific induction in Arabidopsis, is represented by two co-orthologs in the SD legumes, but only one in the LD legumes (Wong et al., 2014).
Another feature of legumes is the expansion of the FT/TFL1 gene family. In Arabidopsis, these genes integrate environmental signaling for induction of flowering, and guide the fate of meristems during inflorescence development. Both major crop legume groups have multiple TFL1 genes and in the galegoid legumes two of these sequences are distinctively divergent from Arabidopsis TFL1 (Foucher et al., 2003; Cronk et al., 2006; Hecht et al., 2011). Legumes also have three distinct subclades of FT genes; FTa, FTb, and FTc (Hecht et al., 2011). Within the large family of MADS domain genes, legumes have additional SVP and SOC1 genes (Hecht et al., 2005; Jaudal et al., 2014), while the FLC clade, which has an important role in vernalization response in Arabidopsis, appears to be absent in the galegoid legumes and at most vestigial in soybean (Hecht et al., 2005; Ruelens et al., 2013).
Genetic Analysis of Flowering in Legumes
Pea (Pisum sativum L.)
Over 20 loci related to flowering time and inflorescence development have been identified in pea (Table 1). Initial work on genetic control of flowering resolved several loci from existing variation among various cultivars of garden and field pea, while other loci were subsequently identified through characterization of induced mutants and specific mutant screens (Murfet, 1985; Weller et al., 1997a, 2009).
Naturally Occurring Variation
Two major loci are known that delay flowering under non-inductive SD. Recessive alleles at the HIGH RESPONSE (HR) locus cause early flowering in SD and reduce, but do not eliminate, the photoperiod response, whereas recessive alleles at the STERILE NODES (SN) locus confer complete daylength insensitivity (Murfet, 1985). Only a single, naturally occurring mutant hr allele has been identified, but for SN both naturally occurring and induced mutant alleles have been described (Liew et al., 2014). Recent work has established HR and SN as pea orthologs of Arabidopsis circadian clock genes ELF3 and LUX, respectively (Weller et al., 2012; Liew et al., 2014), and analysis of sequence diversity suggests a wide distribution of the hr allele across domesticated pea germplasm and an important and ancient role for this mutation in the spring-flowering habit (Weller et al., 2012). In contrast, the main naturally occurring sn allele has a more restricted distribution and occurs only within the subset of lines carrying hr, implying a more recent origin (Liew et al., 2014).
The third locus, LATE FLOWERING (LF), inhibits flowering in both long and short days, and was identified over 10 years ago as a divergent homolog of TFL1 (Foucher et al., 2003). Numerous allelic variants of LF are known, including both naturally occurring and induced mutant alleles. Accessions in which the LF gene is deleted or inactivated by nonsense mutation show extremely early, photoperiod-insensitive initiation of flowering (Murfet, 1985; Foucher et al., 2003), but remain responsive to photoperiod in several other respects, suggesting that LF is not involved directly in the photoperiod response mechanism.
The fourth locus, EARLY (E), is the least well-understood of the naturally variant loci. Dominant alleles of E confer early initiation of flowering in some genetic backgrounds, but this effect shows complex interactions with other loci and incomplete penetrance. Recent identification of a major-effect quantitative trait loci (QTL) for flowering time in a chromosomal location similar to E (Lejeune-Hénaut et al., 2008; Weller et al., 2012) may help in its future molecular characterization.
Allelic differences at the HR, SN, LF, and E loci interact to specify an extremely wide range of flowering times in plants in non-inductive conditions. This range extends from the genotype lf sn which may flower as early as node 7 and is completely insensitive to photoperiod, to genotype LF SN HR e which flowers relatively late under LD and may not flower at all under SD (Murfet, 1985; Weller et al., 2012). Interestingly, most mutagenesis programs in pea have been conducted in spring-flowering (hr) cultivars, and in some cases in lines that also carry sn or lf alleles, and many are also likely to carry derived alleles at the E locus. Mutants isolated from these programs therefore carry at least one additional mutation affecting flowering time, and potentially as many as four.
Induced Mutants – Photoperiod Response
In addition to the SN and HR loci, several other photoperiod response loci have been identified through analysis of induced mutants. Two of these, DIE NEUTRALIS (DNE) and PHOTOPERIOD (PPD) have a role similar to SN, as recessive dne and ppd mutants show early flowering in SD. In the presence of hr, these mutations confer complete photoperiod insensitivity for flowering and other traits (King and Murfet, 1985; Arumingtyas and Murfet, 1994). DNE is the pea ortholog of another circadian clock gene, ELF4 (Liew et al., 2009), but PPD has not yet been identified. In Arabidopsis, the proteins encoded by ELF3, ELF4, and LUX genes participate in the so-called evening loop of the circadian clock and work together in a complex termed the evening complex (EC; Nagel and Kay, 2012), which may provide a mechanistic explanation for the fact that mutants for HR/PsELF3, DNE/PsELF4, and SN/PsLUX have similar phenotypes.
Loci involved in promoting flowering in pea under inductive (LD) conditions have also been identified. Mutants for the phyA photoreceptor were first identified in screens for seedling photomorphogenesis and subsequently shown to have a LD-specific late-flowering phenotype (Weller et al., 1997a). The phyA mutants are largely insensitive to LD, although day extensions with artificial light rich in blue or far-red wavelengths can result in earlier flowering, implying a contribution from other photoreceptors (Weller et al., 1997a; Platten et al., 2005a). While phyB and cry1 might seem plausible candidates for this activity, evidence from phyB and cry1 mutants suggests that neither is fundamentally involved in promotion of flowering (Weller et al., 2001; Platten et al., 2005a). The importance of PHYA is underlined by the dominant early flowering photoperiod-insensitive phyA-3D mutant, which has a higher level of phyA protein due to increased protein stability (Weller et al., 2004). Other loci LATE1 and LATE2 have been identified in specific mutant screens (Hecht et al., 2007). LATE2 has not yet been identified, but LATE1 is an ortholog of Arabidopsis circadian-clock-related gene GIGANTEA (GI; Hecht et al., 2007). The late1 mutants are similar to phyA mutants with respect to their effect on flowering and photoperiod responsiveness, but have only mild photomorphogenic defects. Similar to Arabidopsis GI, LATE1 shows strongly rhythmic expression, and late1 mutants affect the expression rhythms of key circadian clock genes, confirming that LATE1 has a role in clock function (Hecht et al., 2007; Kim et al., 2012; Weller et al., 2012; Liew et al., 2014).
Mutations at other pea loci affect the flowering transition without significantly interfering with the overall ability of the plant to respond to daylength. Under LD, gigas and vegetative1 (veg1) and veg2 mutants do not produce flowers, but instead show a profuse outgrowth of aerial vegetative branches (Murfet, 1985; Hecht et al., 2011; Berbel et al., 2012; Sussmilch et al., 2015). This phenotype appears to represent a failure to specify the identity of secondary inflorescences and to induce the expression of the floral meristem identity gene PROLIFERATING INFLORESCENCE MERISTEM (PIM), a co-ortholog of AP1 (Taylor et al., 2002; Berbel et al., 2012). GIGAS and VEG1 have been respectively identified as an FT homolog and as a divergent member of the AP1 clade of MADS-domain genes (Hecht et al., 2011; Berbel et al., 2012), and VEG2 was recently shown to be the pea ortholog of FD, an BZIP transcription factor that is an important signaling partner of FT proteins (Sussmilch et al., 2015).
Soybean [Glycine max (L.) Merr.]
At least 10 loci that affect flowering-related characteristics in the SDP soybean have now been described (Table 1). Variation at these loci is responsible for a major proportion of the latitudinal adaptation in soybean, which is grown from tropical regions to 50°N. Cultivars grown at lower latitudes experience a longer growing season and are relatively late to mature, whereas expansion to higher latitudes and completion of the growth cycle within the short summer growing season have required a reduction in sensitivity to the inhibitory effects of LD.
The well-known E series of maturity loci (E1 to E9) confer early flowering and maturity, particularly under non-inductive (LD) conditions (Cober and Morrison, 2010; Watanabe et al., 2012; Kong et al., 2014). With the exception of E6 and the recently described E9 locus, the early flowering alleles at the E loci are recessive (Watanabe et al., 2012; Kong et al., 2014). Addition of early flowering alleles at these loci results in incrementally earlier flowering under LD and improved adaptation to short summers at high latitudes. In contrast, “delayed juvenile” soybean lines are conspicuously later to flower under inductive SD conditions, a trait useful for adaptation to low latitudes generally and spring sowings at middle latitudes (Tomkins and Shipe, 1997). Genetic control of the delayed juvenile trait is not currently clear. One study proposed a single locus (J), with recessive alleles conferring late flowering in SD (Ray et al., 1995), whereas other analyses point to a more complex genetic control involving up to two other genes, one of which may be E6 (Cober, 2011). Flowering time in soybean has also been analyzed as a quantitative trait, and several QTL have been identified, many of which are likely to correspond to known maturity loci (Watanabe et al., 2012). The E1, E2, and E3 loci in particular appear to have been detected in a number of QTL studies and have also been referred to as Flowering Time 1 (FT1), FT2, and FT3, respectively (Yamanaka et al., 2000).
Several of the E loci have been characterized physiologically. As in pea, the effects of individual soybean loci have mostly been examined in genetic backgrounds already carrying hypomorphic alleles at other loci, making it difficult to gain a full picture of the action and interactions of any given locus. Nevertheless, five of the eight loci (E1, E3, E4, E7, E8) appear to specifically affect photoperiod responsiveness (Cober et al., 1996a, 2001, 2010; Cober and Voldeng, 2001). In particular, differential sensitivity of E3 and E4 loci to light quality of an artificial LD implicated them in the phytochrome system (Cober et al., 1996b), and both genes have subsequently been shown to encode phyA-type photoreceptors (Liu et al., 2008; Watanabe et al., 2009). Soybean contains four PHYA genes that consist of two pairs of homeologs, with E3 and E4 representing different homeolog pairs. The homeolog of E4, PHYA1, is apparently functional, whereas the homeolog of E3 carries a deletion and is probably a pseudogene (Watanabe et al., 2009). In most plant systems, phyA is important for de-etiolation under continuous far-red (FR) light. Interestingly, loss of E4 function reduced but did not abolish de-etiolation under FR, whereas loss of E3 function had no effect on this response, even in the absence of E4 (Liu et al., 2008). This suggests that the FR-sensing role during de-etiolation has become subfunctionalized to the E4/PHYA1 pair, and implies that phyA1 may also contribute to photomorphogenic responses. The presence of phyA1 may also explain why the e3 e4 mutant still shows delayed flowering in response to photoperiod extensions rich in far-red light. However, it is clear that three other loci, E1, E7, and E8 also contribute to this response (Cober and Voldeng, 2001; Cober et al., 2010).
Like the pea LATE1 locus, soybean E2/FT2 was also identified as an ortholog of GIGANTEA, through a strategy involving fine mapping, candidate gene analysis and reverse genetics (Watanabe et al., 2011). Although recessive e2 alleles can promote flowering under both LD and SD, E2 is also reported to enhance the photoperiod response and clearly contributes to early flowering and latitudinal adaptation (Jiang et al., 2014). However, one of the most significant developments to emerge from analysis of soybean flowering loci has been the recent molecular characterization of the E1 gene. E1 has a major role in natural variation for flowering in soybean and has the largest effect among the E loci (Yamanaka et al., 2000). Positional cloning of E1 revealed that it possesses a region of weak similarity to the plant-specific B3 domain, in addition to a helix-turn-helix domain and a nuclear localization signal, all suggesting a probable role as a transcription factor (Xia et al., 2012). E1 essentially appears to define a legume-specific gene family, but it is distantly related to the RAV subfamily of B3 domain proteins, which includes the Arabidopsis TEMPRANILLO genes that are also transcriptional repressors of FT (Castillejo and Pelaz, 2008).
Flowering Pathways in Legumes
The FT Gene Family
FT genes are of particular interest for understanding flowering time control, in view of their well-documented roles in integration of environmental signals for flowering and in signaling from the site of photoperiod detection in the leaf to the site of flower formation at the shoot apex (Pin and Nilsson, 2012). The FT gene family has been studied in detail in pea, Medicago, Lotus, and soybean (Kong et al., 2010; Laurie et al., 2011; Yamashino et al., 2013; Zhai et al., 2014). Most species have at least five FT-like genes that comprise three distinct clades unique to legumes; FTa, FTb, and FTc (Hecht et al., 2011). Genes in the FTc group are the most divergent, and are distinguished from Arabidopsis FT and most other FT genes by substitution of several conserved residues.
In pea and Medicago, study of expression patterns and mutant phenotypes suggest that FTa and FTb genes are expressed in leaves and may be important for targets of vernalization and photoperiod responses respectively, whereas FTc genes are expressed only in the shoot apex and may contribute to the integration signals from leaf-expressed FT genes (Hecht et al., 2011; Laurie et al., 2011). All pea FT genes can promote flowering to some extent when expressed in transgenic Arabidopsis (Hecht et al., 2011) but one in particular, FTb2, meets the characteristics of the classical “florigen.” It is expressed specifically in leaves under LD, and its upregulation correlates closely with the physiological induction of flowering and precedes the induction of all other FT genes. In addition, its expression correlates strongly with production of a graft-transmissible flowering stimulus (Hecht et al., 2011). Another pea FT gene, FTa1/GIGAS, is also expressed in leaves, and grafting experiments suggest that it may also generate a mobile flowering signal (Beveridge and Murfet, 1996; Hecht et al., 2011). However, the timing of FTa1 induction is delayed relative to FTb2, and gigas mutants have inflorescence identity defects but respond strongly to daylength. This suggests that the two main FT genes expressed in leaves in pea may both signal to the shoot apex but have different developmental roles. In addition, it appears that pea FT genes may regulate each other (Hecht et al., 2011; Figure 1).
FIGURE 1. Models summarizing interactions between flowering genes in control of flowering time in pea and soybean. Genes that promote flowering are shown in green, and those that inhibit flowering are shown in red. LDs, long days; SDs, short days.
In soybean, two FT genes have been singled out as important promoters of flowering; FT2a (an FTa gene) and FT5a (an FTc gene). Expression of both genes is induced in leaves under inductive (SD) photoperiods, and both promote flowering when overexpressed in either Arabidopsis or soybean itself (Kong et al., 2010; Nan et al., 2014). Whereas FT2a appears to be qualitatively regulated by photoperiod, FT5a is expressed to some extent even in LD suggesting its role may not be restricted to photoperiod response (Kong et al., 2010). Two other FTa genes (FT3a and FT3b) also show significant expression in leaves in SD suggesting they may also participate in promotion of flowering (Kong et al., 2010). Surprisingly, one of the four soybean FTb genes, FT4, shows an opposite pattern of regulation and appears to act as a repressor of flowering. FT4 is induced in leaves in LD, and is able to delay flowering when overexpressed in Arabidopsis (Zhai et al., 2014). Interestingly, FT4 carries a substitution of a highly conserved glycine (G133R) in an important functional region, and the significance of this is supported by the fact that the same residue is also substituted in another FT known to repress flowering; FT1 in sugar beet (Pin et al., 2010). However, within the legumes the existence of a repressive FT may be unique to soybean, as all other legume FTb-type sequences known to date carry the canonical glycine in this position.
Response to Photoperiod
In species as diverse as Arabidopsis and rice, the photoperiod-dependent induction of FT genes relies on interactions between light perception and the circadian clock (Andres and Coupland, 2012; Brambilla and Fornara, 2013; Song et al., 2013). It is likely that this is also the case in legumes, in view of the fact that orthologs of PHYA (a photoreceptor) and GI (a gene affecting clock function) are important regulators of photoperiodic flowering in both pea and soybean (Weller et al., 1997a; Hecht et al., 2007; Liu et al., 2008; Watanabe et al., 2009, 2011). The importance of the clock for legume photoperiod responsiveness is further reinforced by the fact that the pea HR, DNE, and SN genes are all orthologs of clock genes and influence clock function (Liew et al., 2009, 2014; Weller et al., 2012). In both soybean and pea, functional variation in PHYA and GI orthologs is clearly associated with differences in the expression of FT genes. Expression of soybean FT2a is elevated by e2, e3, and e4 alleles under long days (Kong et al., 2010; Watanabe et al., 2011) indicating that all three of these E loci participate in a pathway for photoperiod response that converges on FT2a. In the pea late1 and phyA mutants, expression of FTb2 is not detected and other FT genes are more weakly expressed (Hecht et al., 2011), whereas expression of multiple FT genes is elevated in dne and sn mutants (Liew et al., 2009, 2014). These interactions are summarized in Figure 1.
Unfortunately, we do not yet have a clear picture of how these clock and photoreceptor inputs are integrated to provide photoperiod-specific regulation of FT genes. The paradigm for integration of light and clock signals in photoperiod measurement has been established in Arabidopsis and centers on the B-box transcription factor CONSTANS (CO), which is a direct transcriptional activator of FT (Tiwari et al., 2010). LD-specific induction of FT is achieved through transcriptional and post-translational regulation of CO. GI associates with the blue-light photoreceptor FKF1 to provide light-dependent promotion of CO transcription via degradation of the CDF family of CO transcriptional repressors (Andres and Coupland, 2012; Song et al., 2013). In contrast, phyA acts at the post-translational level by stabilizing CO protein under FR light, possibly through antagonism of CO degradation by the COP1 ubiquitin ligase complex (Andres and Coupland, 2012; Song et al., 2013) Although the GI-CO-FT regulatory relationship is also functionally significant in the SDP rice (Brambilla and Fornara, 2013), evidence for the more general conservation of this mechanism across flowering plants is limited (Ballerini and Kramer, 2011), which raises the question of whether it may operate in legumes.
Soybean contains four genes orthologous to Arabidopsis CO (Wong et al., 2014) and all four are reported to promote flowering in transgenic Arabidopsis (Wu et al., 2014), but their endogenous role has not yet been determined. In addition, although the GmCOL1a and GmCOL1b genes showed higher expression levels under SD (Wu et al., 2014) and show some overlap with FT genes in their diurnal expression pattern, it is still unclear whether these genes are transcriptionally regulated by any of the E loci or whether they in turn regulate any of the FT genes. The situation in the galegoid legumes is simpler, with only a single CO ortholog (COLa) known to be present (Hecht et al., 2005; Yamashino et al., 2013; Wong et al., 2014). While the function of this gene has not been directly investigated in pea, its expression is not misregulated in either late1 (Psgi) or dne (Pself4) mutants, despite strong defects in FT regulation, flowering and photoperiod responsiveness in both mutants (Hecht et al., 2007, 2011; Liew et al., 2009). In addition, expression analyses, transgenic studies and characterization of specific mutants in M. truncatula also indicate that COLa does not have any substantial role in flowering time regulation, and suggest that the same is probably true for other COL genes (Wong et al., 2014).
The available evidence so far thus indicates that legume CO-like genes may not have a major role in integration of responses to photoperiod in the temperate legume group, and suggests that some alternative mechanism must be operating. One possibility is that the E1 gene may participate in this role. Analysis of soybean e1 mutants and E1 overexpression lines clearly show that E1 regulates expression of FT genes, including repression of FT2a and FT5a (Thakare et al., 2011; Xia et al., 2012) and induction of the repressive FT4 (Zhai et al., 2014; Figure 1). E1 is specifically expressed under LD, where it shows a strong diurnal expression rhythm, and is also transcriptionally regulated by E4 (Xia et al., 2012), suggesting that regulation by light and the circadian clock may be important for its function. In future, it will be interesting to learn whether E1 is also regulated by E2 and E3, and whether E1 orthologs also regulate flowering in the temperate legumes. However, even if E1 does participate as a key integrator in the soybean photoperiod response mechanism, the fact that it is a repressor of FT suggests that there still may be undiscovered components required for upregulation of FT genes in inductive conditions.
One possible scenario for CO-independent FT induction in legumes is provided by a recent study in Arabidopsis which showed that GI can bind directly to the FT promoter to activate FT transcription in a CO-independent manner (Sawa and Kay, 2011), and it can also interact physically with TEM proteins, which are direct transcriptional repressors of FT distantly related to E1 (Castillejo and Pelaz, 2008; Sawa and Kay, 2011). It is possible that legume E1 and GI orthologs might interact in a similar way. Another scenario may be that the DNA binding and protein-interacting properties of CO may be partitioned into two separate proteins, as has recently been suggested in sugarbeet, where a CCT-domain pseudo-response regulator (PRR) protein (similar to the C-terminal domain of CO) and a B-box zinc finger protein (similar to the N-terminal domain of CO) may interact to confer CO function (Dally et al., 2014).
In addition, the fact that PHYA and GI orthologs are central components of the photoperiod response mechanism in both LDP pea and SDP soybean, but show opposite effects on flowering and FT expression in these two species, implies that the SD/LD difference results from a reversed regulatory interaction at some point downstream of both genes. The relatively close taxonomic relationship between these two species make them an attractive model for understanding the evolution of this difference in photoperiod response mode.
Response to Vernalization
Regulation of flowering by vernalization is a phenomenon widespread across annual species from temperate regions, but is thought to have evolved independently in different plant lineages. As a result, the genes and genetic mechanisms conferring vernalization responsiveness are likely to differ across different groups (Kim et al., 2009). In legumes, the first insight into the genetic control of vernalization response has come from work in M. truncatula, where a survey of Medicago FT genes showed that two tandemly arranged FT genes (FTa1 and FTa2) are induced by vernalization but have different temporal patterns of response (Laurie et al., 2011). FTa2 is induced during exposure to cold, but FTa1 is only expressed following return to warm conditions. Loss-of-function FTa1 insertion mutants are insensitive to vernalization but retain sensitivity to photoperiod, indicating that FTa1 is necessary for response to vernalization, and may be the key target in the legume vernalization pathway (Figure 1; Laurie et al., 2011). Interestingly, lines carrying insertions close to but not within FTa1 coding regions show dominant inheritance of early, vernalization-independent flowering, which suggests that FTa1 is normally subject to repression by adjacent regulatory regions and that this repression is normally overcome by vernalization (Jaudal et al., 2013).
Control of Flowering in Other Legumes
Flowering time control is a key issue in adaptation of many other crop legumes (Summerfield and Roberts, 1985b; Nelson et al., 2010), and loci controlling flowering time and other flowering-related traits have now been identified in most crop and model legumes (Table 2). The majority of these loci have been detected as QTL, but in some cases they have been amenable to classical genetic analyses and Mendelian inheritance has been defined. It is likely that some of the same loci have been detected in different studies but it is difficult to assess this due to the lack of markers in common and/or sequence information.
TABLE 2. List of flowering time QTL in legumes, indicating the linkage group (LG) on which they occur.
While all of this variation is naturally arising and therefore likely to be adaptive, several loci can be singled out for a particularly significant contribution to adaptation and range expansion. One example is the SDP common bean (Phaseolus vulgaris), where, like soybean, expansion to higher latitudes has been accompanied by earlier flowering under LD and a reduction in photoperiod responsiveness (Gepts and Debouck, 1991). A significant proportion of this variation can be attributed to PPD, a mendelized locus on LG1, where recessive alleles confer reduced photoperiod response and early flowering under LD (Koinange et al., 1996). A second example is narrow-leafed lupin (Lupinus angustifolius), where the acquisition of early, vernalization insensitive flowering conditioned by dominant alleles at the the Ku locus has been integral to deployment of this crop for Mediterranean climates with mild winters in which a vernalization requirement would not be met (Nelson et al., 2010). A third example is lentil (Lens culinaris), where an early flowering variant at the Sn locus has had an important role in developing early flowering cultivars for water-limited environments and broadening the genetic base of lentil in south Asia (Sarker and Erskine, 2006).
There is significant potential for translation of insights from the pea and soybean systems to achieve a better understanding of other legume species. This potential reflects advances in two areas. First, functional and phylogenetic analyses of flowering genes and gene families in pea and soybean can improve the identification of plausible candidate genes for particular loci. Second, availability of sequenced genomes and gene-based genetic maps have improved the technical ability to identify and evaluate candidate genes under QTL, and to identify those QTL that may have conserved locations across several species. In addition the fact that certain desirable traits such as early, photoperiod-insensitive flowering or determinate growth can result from simple monogenic loss-of-function mutations means that in species where such variants do not already exist it may be feasible to generate them through mutagenesis.
Within the legumes the value of a comparative approach is most clearly shown by recent findings that in several species, determinate inflorescence architecture is conferred by mutation of specific TFL1 genes [described by Benlloch et al. (2015) in this Research Topic]. A second example is the recent identification of the lentil SN locus as the ortholog of pea HR (Weller et al., 2012), suggesting that the nature of flowering time adaptation may be widely conserved. In addition to these well-established examples, it is now also possible to identify other potentially conserved QTL and to begin to speculate about their nature (Figure 2).
FIGURE 2. Relative locations of flowering time gene homologs and quantitative trait loci (QTL) in the chickpea genome. Chromosomes are represented as bold vertical lines with marker/gene positions indicated in Mbp. QTL are shown as vertical bars, and the markers delimiting them are indicated by gray boxes. References for each QTL can be found in Table 2.
The most prominent case is the existence of a conserved major flowering time QTL in a region syntenic with a section of Medicago chromosome 7 containing a tandem array of FTa and FTc genes. This region is now implicated in control of flowering time in numerous members of the temperate legume clade, including M. truncatula itself (Pierre et al., 2008), faba bean (Cruz-Izquierdo et al., 2012), chickpea (Cobos et al., 2009; Aryamanesh et al., 2010), narrow-leafed lupin (Nelson et al., 2006), L. japonicus (Gondo et al., 2007) and alfalfa (Robins et al., 2007). As described above, functional studies in Medicago and pea have demonstrated the importance of FT genes in this cluster for vernalization responsiveness and other aspects of flowering (Laurie et al., 2011), and this implies that disruption to one or more of these genes is the most likely molecular basis for these QTL. Evidence from Medicago and pea indicates that FTa and FTc genes promote flowering, and a simple loss-of-function mutation would therefore be expected to be recessive and late-flowering. However, for several of these QTL the “derived” form appears to be early flowering, as the later-flowering variant is much more widespread and likely to be ancestral (faba bean, chickpea, lupin), and at least in lupin and chickpea the early flowering trait has been reported to show dominant inheritance (Aryamanesh et al., 2010; Nelson et al., 2010). These observations suggest that if genes in the FTa/c cluster are the basis for these QTL, the genetic changes are likely to be gain-of-function mutations, and it might also be expected that one or more of the FT genes in the cluster would show high and/or de-regulated expression. This also suggests that the causal genetic changes could be varied and complex, potentially involving variation in copy number or alteration to promoter or other regulatory regions, as observed for gain-of-function mutations affecting flowering time genes in cereals (e.g., Beales et al., 2007; Nitcher et al., 2013).
A closer look at individual species provides additional illustrations of a comparative approach to candidate gene identification. The first example is common bean where, in addition to several flowering time QTL (Table 2), two loci controlling photoperiod response have also been characterized; Ppd and Hr (Gu et al., 1998). The Ppd locus has been mapped to within 5 cM of the FIN locus controlling shoot determinacy (Kwak et al., 2008), and the molecular identity of FIN as a TFL1 co-ortholog (Repinski et al., 2012) therefore indicates the approximate genomic region in which PPD is located. This region is syntenic with the region in soybean containing the E3/PHYA3 gene (McClean et al., 2010) and, as expected, contains the bean E3 ortholog, suggesting this as an attractive candidate for the PPD locus. A second bean locus contributing to photoperiod sensitivity, Hr, is less well-defined but is positioned toward the other end of the same linkage group (Gu et al., 1998), a region that contains homologs of ELF3 and the FTa/c cluster. A third locus identified as a QTL in LG9 is located near the bean ortholog of ZEITLUPE, a gene important for circadian clock regulation in Arabidopsis (Tar’an et al., 2002; Kwak et al., 2008).
The second example is chickpea, where classical genetic analyses have distinguished four Mendelian loci, named Early flowering 1 (Efl1) to Efl4 (Gaur et al., 2015). Recessive alleles at these loci confer early flowering and at least two are likely to be widespread within the chickpea germplasm and have a major impact on flowering time adaptation. In addition, many linkage studies have been performed in chickpea, and six flowering time QTL have been defined in LG1, 2, 3, 4, and 8 (Table 2). Some of these studies have involved parents known to carry efl1 or efl2, suggesting that QTL may correspond to major loci in some cases. This, together with the availability of the chickpea genome sequence (Jain et al., 2013; Varshney et al., 2013) enables an assessment of approximate co-location between flowering gene homologs and flowering time loci or QTL (Figure 2). For example, Efl1 was defined in a cross using the early flowering line ICCV2 (Kumar and van Rheenen, 2000), which has also been used as a common parent in several studies reporting a major QTL (Cho et al., 2002; Vadez et al., 2012; Jamalabadi et al., 2013). Although its genomic location is still uncertain (as markers near the QTL have been variously assigned to LG3, 4, 5, 6, and 8), the clearest and most recent indication is given by Jamalabadi et al. (2013) who placed a major QTL between markers TA117 and STMS22, which both map to LG5 (Radhika et al., 2007; Hiremath et al., 2012). The latter is physically located near genes responsible for flowering time variation in other species such as ELF3 or ELF4, but also LEAFY (LFY), which is involved in flower initiation and inflorescence development (Hofer et al., 1997). Recessive alleles at the photoperiod response locus Efl2 are present in the cultivar ICC5810 (Or et al., 1999), a line also used as a parent by Lichtenzveig et al. (2006), who found a major QTL in LG1 explaining 60% of the flowering time variation. This chromosomal region contains several genes with the potential to explain these differences, including orthologs of PHYB and TFL1.
For the remaining reported QTL, there is no clear relationship to major flowering loci, but some potential candidates can be identified, including PHYA and GI for the LG4 QTL, another member of the FT family (FTa3) for the LG2 QTL, and a FD-like gene for the LG8 QTL (Figure 2). The QTL in the central region of LG3 deserves special attention as it has been reported several times (Table 2). The presence of the FTa/c cluster as the most likely candidate has been already mentioned, but other genes within the interval are also noteworthy, including, two CYCLING DOF FACTOR (CDF) homologs, a LUX-like gene, and an ortholog of the CO-like gene COLh. This last gene has also been highlighted as a candidate near the chromosome 7 QTL in M. truncatula (Pierre et al., 2011). A second QTL close to the bottom of chickpea LG3 has also been described (Aryamanesh et al., 2010), in a region containing genes involved in circadian clock and light signaling, including PRR and phytochrome-interacting factor (PIF) homologs, a PHYA paralog, and the ortholog of LATE ELONGATED HYPOCOTYL (LHY).
Detailed genetic studies in model legumes are bringing rapid progress to our understanding of flowering time control, and have identified significant similarities and differences with other plant groups. At the same time, new genome sequences and dense, gene-based genetic maps are accelerating the translation of these insights to a range of other legume species, and giving new insight into how flowering time gene functions may be conserved or diversified within this important group of crops. It now seems reasonable to expect that genes underlying most of the major flowering time loci in legumes will be identified within the next 5–10 years, which will help improve our understanding of how they work together to provide adaptation to specific locations and agronomic constraints.
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.
We thank F. Sussmilch and R. Macknight for helpful comments on the manuscript, and the Australian Research Council for financial support through Discovery Project and Future Fellowship grants (JLW).
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Keywords: legume, flowering, photoperiod, pea, soybean
Citation: Weller JL and Ortega R (2015) Genetic control of flowering time in legumes. Front. Plant Sci. 6:207. doi: 10.3389/fpls.2015.00207
Received: 04 February 2015; Accepted: 15 March 2015;
Published online: 09 April 2015.
Edited by:Rafael Lozano, University of Almeria, Spain
Reviewed by:Steven B. Cannon, United States Department of Agriculture – Agricultural Research Service, USA
Matthew Nicholas Nelson, University of Western Australia, Australia
Michael Grillo, University of Illinois, USA
Copyright © 2015 Weller and Ortega. 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: James L. Weller, School of Biological Sciences, University of Tasmania, Private Bag 55, Hobart, TAS 7001, Australia firstname.lastname@example.org