Parallel evolution of TCP and B-class genes in Commelinaceae flower bilateral symmetry
© Preston and Hileman; licensee BioMed Central Ltd. 2012
Received: 12 December 2011
Accepted: 6 March 2012
Published: 6 March 2012
Flower bilateral symmetry (zygomorphy) has evolved multiple times independently across angiosperms and is correlated with increased pollinator specialization and speciation rates. Functional and expression analyses in distantly related core eudicots and monocots implicate independent recruitment of class II TCP genes in the evolution of flower bilateral symmetry. Furthermore, available evidence suggests that monocot flower bilateral symmetry might also have evolved through changes in B-class homeotic MADS-box gene function.
In order to test the non-exclusive hypotheses that changes in TCP and B-class gene developmental function underlie flower symmetry evolution in the monocot family Commelinaceae, we compared expression patterns of teosinte branched1 (TB1)-like, DEFICIENS (DEF)-like, and GLOBOSA (GLO)-like genes in morphologically distinct bilaterally symmetrical flowers of Commelina communis and Commelina dianthifolia, and radially symmetrical flowers of Tradescantia pallida.
Expression data demonstrate that TB1-like genes are asymmetrically expressed in tepals of bilaterally symmetrical Commelina, but not radially symmetrical Tradescantia, flowers. Furthermore, DEF-like genes are expressed in showy inner tepals, staminodes and stamens of all three species, but not in the distinct outer tepal-like ventral inner tepals of C. communis.
Together with other studies, these data suggest parallel recruitment of TB1-like genes in the independent evolution of flower bilateral symmetry at early stages of Commelina flower development, and the later stage homeotic transformation of C. communis inner tepals into outer tepals through the loss of DEF-like gene expression.
KeywordsB class genes Commelinaceae CYCLOIDEA homeotic change monocots tepals teosinte branched1
Evolutionary transitions between flower radial symmetry (polysymmetry and actinomorphy) and bilateral symmetry (monosymmetry and zygomorphy) have occurred multiple times independently across angiosperms, and are associated with increased pollinator specialization and speciation rates [1–6]. Indeed, some of the largest angiosperm families have species with predominantly bilaterally symmetrical flowers, including the legumes (Leguminosae, rosids, core eudicots), daisies (Asteraceae, asterids, core eudicots) and orchids (Orchidaceae, monocots) . Recent functional studies in distantly related core eudicots - including Antirrhinum majus (Plantaginaceae), Iberis amara (Brassicaceae), Pisum sativum and Lotus japonicus (Leguminosae) and Gerbera hybrida (Asteraceae) - have demonstrated a role for class II T EOSINTE BRANCHED1 (TB1)/C YCLOIDEA (CYC)/P ROLIFERATING CELL NUCLEAR ANTIGEN GENE-CONTROLLING ELEMENT BINDING FACTOR (PCF) (TCP) transcription factors in establishing flower symmetry by specifying identity to the dorsal (adaxial) region of the flower [8–13]. Since bilateral symmetry has evolved independently in these lineages, genetic data suggest parallel recruitment of class II TCP genes in the evolution of a convergent trait [11, 14–16]. Whether homologous TCP genes have been similarly utilized in monocot flower bilateral symmetry remains largely untested [but see [17, 18]].
The genetic basis of flower bilateral symmetry is best understood in the model species A. majus, and involves the action of four asymmetrically expressed transcription factors [8, 9, 19–21]. Dorsal identity is specified by the class II TCP genes CYCLOIDEA (CYC) and DICHOTOMA (DICH), and the MYB gene RADIALIS (RAD), whereas ventral (abaxial) identity is conferred by the MYB gene DICHOTOMA (DICH). CYC and DICH are derived from a recent duplication event at the base of the Antirrhineae tribe , and have distinct but overlapping functions, as inferred from their mutant phenotypes [8, 9]. Whereas wild type A. majus plants have five petals, four stamens and a dorsal staminode, cyc single mutants often have extra dorsal petals that are reduced in size, and a fully developed dorsal stamen. By contrast, dich single mutants only lack the internal asymmetry of wild type dorsal petals. Together with the fully ventralized, and, hence, radially symmetrical flowers of cyc:dich double mutants, these data demonstrate a role for CYC in dorsal stamen abortion, petal growth and organ number determination, and a role for DICH in shaping dorsal petal growth [8, 9].
A similar range of dorsal identity functions has been assigned to CYC-like genes of other core eudicots, including Linaria vulgaris, P. sativum, I. amara, Lotus japonicus, and G. hybrida[10–13, 20, 23]. Furthermore, although monocots do not have a strict CYC gene ortholog due to two separate duplication events at the base of core eudicots , the observation that the class II TCP gene RETARDED PALEA1 (REP1) in Oryza sativa (rice, Poaceae) is expressed only in the dorsally positioned palea, suggests further recruitment of TCP genes in the evolution of monocot flower bilateral symmetry . Indeed, it was recently found that bilaterally symmetrical flowers of Costus spicatus (Costaceae; Zingiberales) and Heliconia stricta (Heliconiaceae) have asymmetric TCP gene (CsTB1a and HsTBL2b, respectively) expression at early to late stages of flower development . However, in contrast to the core eudicots, CsTB1a and HsTBL2b expression is restricted to the ventral, rather than the dorsolateral, side of the flower .
In addition to a hypothesized role for TCP genes, the floral homeotic B-class genes DEFICIENS (DEF) and GLOBOSA (GLO) have been implicated in the multiple independent derivations of flower bilateral symmetry in monocots [25–29]. Evidence supporting this comes largely from the observation that DEF-like gene paralogs are differentially expressed in the morphologically distinct outer tepals, dorsolateral inner tepals and ventral inner tepal (lip or labellum) of Phalaenopsis equestris (Orchidaceae) [25, 26]. In both core eudicots and monocots, DEF- and GLO-like proteins function as obligate heterodimers to confer identity to the second and third whorls, although there are exceptions [30, 31]. In the second whorl of Arabidopsis thaliana (Brassicaceae) and A. majus APETALA3 (AP3)/DEF and PISTILLATA (PI)/GLO form tetramers with SEPALLATA (SEP) and APETALA1 (AP1)/SQUAMOSA (SQUA) MADS-box proteins, resulting in the activation of downstream genes that confer petal identity [32–36]. Thus, since DEF/GLO-, and to a lesser extent SEP- and SQUA-like, gene function is largely conserved across angiosperms [37–45], shifts between radial and bilateral perianth symmetry could be explained by changes in expression of these floral homeotic genes, resulting in the loss, gain or modification of second whorl identity.
Based on detailed analyses of flower development, and the known role of class II TCP genes in core eudicots, Hardy et al. (2009) recently hypothesized a role for TB1-like TCP genes in establishing bilateral symmetry in early developmental stages of Commelina flower development . Furthermore, we propose a second, non-exclusive hypothesis, that dorsal-specific expression of DEF/GLO-like genes defines the dorsoventral axis of symmetry in mid- to late-stage C. communis corollas. In this study, we use gene expression and micromorphological data to test three predictions of these hypotheses that: (1) TB1- like genes are asymmetrically expressed in bilaterally symmetrical C. communis and C. dianthifolia, but not radially symmetrical Tradescantia (formerly Setcreasea) pallida, corollas consistent with a role in differential organ growth, (2) DEF and GLO orthologs are co-expressed in staminodes, stamens and the dorsolateral inner tepals, but not in outer tepals or the outer tepal-like ventral inner tepal of C. communis, and (3) cellular morphology of the C. communis ventral inner tepal is more similar to outer tepals than dorsolateral inner tepals, suggesting asymmetric loss of inner tepal identity in the second whorl.
Inflorescence material was harvested from wild-collected, flowering individuals of C. communis and T. pallida in Missouri and Kansas (USA) during the summer months, and from C. dianthifolia plants grown under standard greenhouse conditions at the University of Kansas. For scanning electron microscopy (SEM) and in situ hybridization, whole inflorescences were fixed overnight in formalin acetic alcohol (FAA: 47.5% (v/v) ethanol, 5% (v/v) acetic acid, 3.7% (v/v) formaldehyde), and gradually taken through an alcohol series to 100% ethanol. For quantitative reverse transcriptase polymerase chain reaction (qRT-PCR), flower organs from 10 to 16 flowers were individually dissected twice from 3 to 5 mm long buds, pooled according to identity/position, and snap-frozen in liquid nitrogen. Total RNA was extracted using TriReagent (Applied BioSystems, Carlsbad, CA, USA), DNA contamination was removed using TURBO DNase (Applied BioSystems), and 1 μg of RNA was reverse transcribed using the iScript Select cDNA synthesis kit (Bio-Rad, Hercules, CA, USA). Genomic DNA was extracted from leaf material using the DNeasy Plant Mini Kit (Qiagen, Valencia, CA, USA).
Ethanol-dehydrated inflorescences were dissected to reveal internal floral organs as necessary. Tissues were critical point dried in a Tousimis critical point drier, mounted on stubs, sputter-coated with gold and viewed with a D. Leo field emission scanning electron microscope (VTT, Espoo, Finland). For micromorphological analyses of inner and outer tepals, both adaxial and abaxial surfaces were analyzed at regions proximal, medial and distal to the floral axis.
Gene isolation and phylogenetic analysis
In order to isolate and sequence all TB1-like orthologs from genomic DNA of C. communis, C. dianthifolia and T. pallida, we used the degenerate forward primers, CYCF1, CYCF2, CYC73aaF, CYC73bF, which were previously designed to amplify CYC/TB1 genes from a wide range of angiosperm taxa, in combination with the reverse primers CYCR1 and CYCR2 [56, 57]. Amplicons were cloned into the pGEM-T vector (Bio-Rad), and 5 to 10 colonies per successful PCR reaction were sequenced. To determine if the Commelinaceae sequences corresponded to CYC/REP/TB1-like genes, and to determine orthology and copy number, amino acid sequences spanning the TCP to R domain from C. communis, C. dianthifolia and T. pallida were aligned by MAAFT [58, 59] and then by eye in MacClade  with previously designated CINCINATTA (CIN)-like, CYC-like, REP-like and TB1-like TCP genes [24, 61]. Nucleotide alignments were subjected to maximum likelihood (ML) analyses in GARLI 0.951 and Bayesian analyses in MrBayes 3.1.2 following model optimization in MrModelTest [62–64]. ML analyses were run using 10 random addition sequences with 500 bootstrap replicates. Bayesian analyses were run twice for 10 million generations, sampling every 1,000 generations, with 25% of trees discarded as burn-in. Newly generated TB1-like sequences were submitted to Genbank with accession numbers [Genbank: JQ622131-JQ622135 and JQ622142].
DEF and GLO orthologs were isolated and sequenced from cDNA of C. communis, C. dianthifolia and T. pallida using previously described degenerate primers . Amplicons were cloned and sequenced as previously described, and aligned nucleotide sequences were subjected to ML and Bayesian analyses as described for the TB1-like genes. Newly generated DEF- and GLO-like genes were submitted to Genbank with accession numbers [Genbank: JQ622136-JQ622141].
To compare patterns of TB1-like and B-class gene expression in mid-stage floral organs of T. pallida, C. dianthifolia and C. communis, qRT-PCR analyses using DyNAzyme II Hot Start DNA Polymerase (GE Healthcare, Pittsburgh, PA, USA) and SYBR Green I (Invitrogen, Carlsbad, CA, USA) were conducted on a DNA Engine Opticon 2 real-time PCR machine (MJ Research. Waltham, MA, USA) as previously described . Two primers pairs per target gene were designed in Primer 3, and the most efficient primer pair was selected for expression analysis (Additional file 1) . Where possible, primer pairs were designed to span introns to rule out DNA contamination. β-ACTIN (ACT) and EUKARYOTIC TRANSLATION ELONGATION FACTOR 1 ALPHA 1 (EF1alpha) showed little transcriptional variation across different tissues of C. communis and C. dianthifolia, and T. pallida, respectively, and were, therefore, selected as reference genes. A negative cDNA control containing RNA from dorsolateral inner tepals and lacking the reverse transcriptase enzyme was initially used as a negative control template for all qRT-PCR analyses. Furthermore, when no transcription was detected in floral material, genomic DNA was used as a positive control. For each gene the mean and standard deviation was determined for three to four technical replicates. Results were analyzed separately for one (C. dianthifolia) or two (C. communis and T. pallida) biological replicates to account for differences in developmental staging of the pooled material, and compared for consistent results between organ type and organ position. Analyses were not carried out for C. dianthifolia outer tepals due to difficulty obtaining good quality RNA from these organs.
In situ hybridization
To better determine the spatio-temporal pattern of gene expression, in situ hybridization was carried out in wax-embedded inflorescence tissues of the most closely related species, C. communis (DEF, GLO and TB1a) and C. dianthifolia (DEF and TB1a). Antisense and sense gene-specific probes of CcDEF (for both species), CcGLO (C. communis only), CcTB1a (C. communis only) and CdTB1a (C. dianthifolia only) were generated using T7 and SP6 RNA Taq polymerase (Roche Applied Science, Indianapolis, IN, USA) according to the manufacturer's instructions. Each probe spanned ca. 400 bps, and included part of the C-terminal domain and the 3'-untranscribed region. As an experimental control, an antisense probe was generated for CcHistone4 as described previously . In situ hybridization was performed as described previously [68, 69].
Flower development and perianth micromorphology
Comparative morphological analyses revealed a similar progression of flower development for C. communis and C. dianthifolia at early to mid stages. In both species, development proceeded asymmetrically, with the ventral/lateroventral organs developing more rapidly than the dorsal/dorsolateral organs (Figure 2J, K). In the outer tepal and stamen whorls, this asymmetry was maintained into late stage development for both species (Figure 2D, E, G, J, K). By contrast, at mid to late stages of development the ventral inner tepal of C. communis, but not C. dianthifolia, arrested prematurely. This resulted in strong asymmetry in the mature corolla of C. communis, with the ventral inner tepal resembling the small colorless outer tepals (Figure 2D, G versus 2E, H). Unlike C. communis and C. dianthifolia, flowers of T. pallida were radially symmetrical from early to late stages of development (Figure 2F, I, L).
Gene duplication in the TB1-like gene lineage
Differential expression of TB1-like genes
Unlike tepals, the correlation between TB1a expression and stamen differentiation was only weakly supported. In C. communis, although TB1a was asymmetrically expressed in dorsal staminodes versus ventral stamens, the direction of differential expression contrasted between replicates (Figure 5 and Additional file 2). This suggests dynamic expression of TB1a at mid stage stamen development. By contrast, TB1a expression was weak but consistently higher in dorsal staminodes versus ventral stamens of C. dianthifolia (2.3-fold difference for biological replicate one (Figure 5); detectable in dorsal staminodes but undetectable in ventral stamens for biological replicate two (data not shown)), and was not significantly different between dorsal and ventral stamens of T. pallida (1.2-fold difference for one biological replicate) (Figure 5). In contrast to qRT-PCR analyses, no TB1a expression was detectable in early to late stage flowers of C. communis, C. dianthifolia or T. pallida using in situ hybridization (data not shown). This suggests that TB1a transcripts are below the level of detection using this method.
QRT-PCR analyses of TB1b genes revealed different expression patterns relative to TB1a paralogs (Figure 5 and Additional file 2). In T. pallida, TB1b was undetectable in all floral organs and leaves, despite amplification of genomic DNA (Figure 5 and Additional file 2). In C. communis, TB1b expression was highest in leaves, with low (Figure 5) to no (Additional file 2) detectable expression in all other organs. For both replicates, no significant differences in transcript levels were detected between dorsal and ventral organs (Figure 5 and Additional file 2). Finally, for C. dianthifolia, no TB1b expression was detected in any floral organ, again despite amplification of genomic DNA (Figure 5).
Differential expression of B-class genes
To test the prediction that B-class gene expression is exclusively reduced or absent from the outer tepal-like ventral inner tepal of C. communis, DEF and GLO genes were isolated from all three focal species, and both qRT-PCR and in situ hybridization analyses were carried out on inflorescence tissues. ML and Bayesian analyses supported the isolation of both DEF and GLO orthologs from each species, and relationships among a larger set of DEF and GLO genes largely tracked the known species tree for monocots (Additional file 3). As predicted, GLO was expressed in inner tepals and stamens of C. communis, C. dianthifolia and T. pallida (Figure 5 and Additional file 2). Furthermore, analyses revealed low (T. pallida based on one biological replicate) to no (C. communis based on two biological replicates) expression in outer tepals of representative Tradescantia and Commelina species (Figure 5 and Additional file 2). In C. communis, GLO was expressed similarly in dorsolateral and ventral inner tepals, with expression being significantly higher in dorsal staminodes than ventral stamens (2.1-fold difference for two biological replicates (SD = 0.27)) (Figure 5 and Additional file 2). A similar asymmetric expression pattern was detected in the stamen whorls of C. dianthifolia (Figure 5). However, in T. pallida there was no significant difference in expression between ventral versus dorsal inner tepals and stamens for one biological replicate (Figure 5 and Additional file 2).
QRT-PCR analyses revealed DEF gene transcripts in inner tepals and stamens of C. communis, C. dianthifolia and T. pallida (Figure 5 and Additional file 2), with low to no expression of DEF in outer tepals and gynoecia of C. communis and T. pallida (Figure 5 and Additional file 2). In C. communis, DEF expression was significantly higher in dorsal staminodes versus ventral stamens (3.5-fold difference for two biological replicates (SD = 0.32)), and in contrast to dorsolateral inner tepals, was completely absent from ventral inner tepals for two biological replicates (Figure 5 and Additional file 2). In C. dianthifolia, DEF expression was not significantly different between dorsal staminodes and ventral stamens. However, in striking contrast to C. communis, DEF was significantly higher in ventral versus dorsolateral inner tepals (2.3-fold difference for one biological replicate). Finally, in T. pallida, DEF expression was not significantly different between dorsal and ventral stamens, and was highly variable in dorsolateral versus ventral inner tepals between two biological replicates (Figure 5 and Additional file 2).
Consistent with qRT-PCR, in situ hybridization analyses of DEF showed much higher expression levels in dorsal compared to ventral inner tepals of early to late stage C. communis flower buds (Figure 6D-I). However, in the stamen whorls, this dorsoventral gradient of DEF expression only became evident following late-stage differentiation of the ventral stamens (Figure 6D-I). Comparable analyses in C. dianthifolia revealed DEF expression in both dorsolateral and ventral inner tepals, dorsal staminodes and ventral stamens during early to midstages of development (Figure 6J-M). Strong expression was maintained in both the dorsolateral and ventral inner tepals into late development (Figure 5N). However, DEF expression became gradually weaker in ventral stamens relative to dorsal staminodes during late stage anther differentiation (Figure 6M, N). No antisense transcripts of DEF were detectable in outer tepals or gynoecia of C. communis or C. dianthifolia. Furthermore, no staining was observed in control sections of either species using DEF or GLO sense probes (Figure 6O and data not shown).
A major conclusion from this study is that TB1-like genes have been independently recruited in establishing Commelinaceae corolla bilateral symmetry in early development, similar to several core eudicot lineages and rice [8–13, 17]. Furthermore, micromorphological evidence and expression of the B-class MADS-box gene CcDEF suggests that late stage asymmetry between the dorsolateral and ventral inner tepals of C. communis is due to a homeotic transformation of the ventral inner tepal into an outer tepal. In the sections below, we discuss the implications of these results as they relate to our understanding of convergent trait evolution.
Parallel evolution of TB1-like genes across angiosperms
Bilateral flower symmetry can be achieved through the asymmetric loss or reduction of organs (structural zygomorphy) or the modification of organs (presentation zygomorphy) within one or more whorls, and can be present in early and/or late stages of development . Although both types of zygomorphy are found within the monocots, structural zygomorphy is particularly prevalent within the Asparagales (for example, Orchidaceae), Arecaceae, Dasypogonaceae, Zingiberales (for example, Zingiberaceae), Commelinales (for example, Commelinaceae) and Poales (for example, Poaceae) [18, 27, 29, 48, 70]. In most cases, bilateral symmetry affects the inner tepals and stamen whorls. However, outer tepal, inner tepal, stamen and gynoecial zygomorphy have all evolved in the monocots multiple times independently .
Maximum parsimony character state reconstructions support a gain of tepal bilateral symmetry within the Commelina-containing Commelineae clade of Commelinaceae (Figure 1). Available data suggest that members of the Commelineae have flowers that are strongly bilaterally symmetrical in early development, but vary in the strength of structural tepal zygomorphy in late development [54, 71] (this study). For example, although all are strongly zygomorphic in early development, at anthesis C. communis inner tepals are highly differentiated along the dorsoventral axis, whereas C. dianthifolia and Murdannia nudiflora inner tepals are only slightly differentiated in size and shape. Based on evidence from core eudicots, it has been hypothesized that asymmetric expression of CYC/TB1-like genes underlies early stage structural zygomorphy in the Commelineae . Consistent with this hypothesis, TB1a is expressed asymmetrically in tepals of C. communis and C. dianthifolia, but not T. pallida, at mid stages of flower development. However, in contrast to the asymmetric expression of CYC and DICH in the model core eudicot A. majus and REP1 in O. sativa, expression is significantly higher in the ventral, as opposed to dorsolateral, tepals [8, 9, 17] (this study). It is predicted that the asymmetrical expression of TB1a in C. communis and C. dianthifolia is initiated in early flower development and has no effect on late stage development when the ventral inner tepal of C. communis arrests growth (see next section).
In A. majus expression of CYC in the dorsal floral meristem represses growth; a similar repressive function has been assigned to IaCYC of the rosid core eudicot Iberis amara (Brassicaceae) in mid to late stage dorsal petal development [8, 9, 11]. By contrast, at mid to late stages of A. majus flower development, CYC expression in the dorsal petals actually increases cell proliferation and elongation relative to the ventral petal [8, 9]. Together with results from Commelinaceae, these data support developmentally and taxonomically distinct roles for CYC in establishing early to late stage perianth organ growth, and suggest that parallel recruitment of CYC/TB1 genes in floral bilateral symmetry is not limited to the dorsal side of the flower. Indeed, a ventral pattern of expression was recently demonstrated for CsTBL1a in bilaterally symmetrical C. spicatus (Costaceae, monocot) flowers .
Further studies testing the involvement of CYC/TB1 genes in transitions from radial to bilateral flower symmetry will require functional tests, and should aim to elucidate whether changes in CYC/TB1 expression are due to cis-regulatory or upstream changes. In A. majus, the NAC family protein CUPULIFORMIS (CUP) has been implicated in the positive regulation of CYC. Thus, expression analyses of CUP-like genes in perianth organs of Commelinaceae and other monocots varying in flower symmetry might be a good starting point to address this question.
Parallel evolution of B-class genes in monocots
It has been hypothesized that changes in the expression of organ identity genes can explain the evolution of flower bilateral symmetry in certain monocots by altering the identity of a subset of organs within a floral whorl. In the case of orchids, one of several DEF-like genes evolved an asymmetric expression pattern following gene duplication, and is implicated in modification of the ventrally positioned inner tepal into the characteristic lip [25, 27, 73–75]. Our data also support a role for DEF-like gene evolution in modification of the C. communis ventral inner tepal. However, unlike orchids, the modification of DEF-like gene expression in C. communis was not preceded by gene duplication and is presumably not associated with changes in protein function at the biochemical level. Furthermore, unlike C. dianthifolia and T. pallida, the ventral inner tepals of C. communis flowers have stomata on their abaxial surface similar to outer tepals. This micromorphological marker correlates both with the general outer tepal-like appearance of the ventral inner tepal and the complete absence of DEF-like gene expression during early to late stages of development.
Together, these studies suggest parallel evolution of DEF-like genes in the independent origins of monocot flower bilateral symmetry. Future studies in other monocot families will be required to determine the generality of these results, and to test whether evolution of DEF-like gene expression can explain petaloidy in the stamen whorl . Furthermore, a key question remains as to whether evolution of DEF-like gene expression can be explained by cis-regulatory or upstream changes. In A. thaliana, SUPERMAN (SUP), FLORAL ORGAN NUMBER1 (FON1), CUP-SHAPED COTYLEDON1 (CUC1), and CUC2 proteins negatively regulate both B-class genes in the sepal whorl . Thus, expression of these proteins in the ventral inner tepal of C. communis could explain the loss of DEF-like expression in this organ. However, this scenario would require that SUP-, FON1- and CUC1/2-like proteins do not regulate the C. communis GLO-like gene, which is expressed normally in the ventral inner tepal.
Together with other studies, our gene expression data on three morphologically diverse species of Commelinaceae suggest a parallel role for two major transcription factors in the independent evolution of angiosperm flower bilateral symmetry. In the case of class II TCP genes, changes in expression are correlated with early developmental shifts from radial to bilateral flower symmetry in several core eudicots and commelinid monocots (rice, Costus and Commelina). This supports a conserved role for class II TCP genes in organ growth across angiosperms, and suggests either evolutionary constraint on the flower symmetry gene network or the involvement of few genes in the establishment of floral meristem symmetry. Evolution of DEF-like genes is also implicated in shifts from radial to bilateral flower symmetry, at least within divergent monocots (Phaelaenopsis and C. communis). However, in contrast to class II TCP genes, changes in both function (Phaelaenopsis) and regulation (C. communis) of B-class genes are implicated in late developmental shifts in within-whorl organ identity. Further studies are required to test the generality of class II TCP and B-class gene evolution in diversification of monocot flowers, and to decipher whether/why the same genes have been the targets of repeated selection across millions of years of angiosperm diversification.
EUKARYOTIC TRANSLATION ELONGATION FACTOR 1 ALPHA 1
FON1 FLORAL ORGAN NUMBER1
PCF PROLIFERATING CELL NUCLEAR ANTIGEN GENE-CONTROLLING ELEMENT BINDING FACTOR
Bayesian posterior probability
quantitative reverse transcriptase polymerase chain reaction
RETARDED PALEA 1
TB1 teosinte branched1
We thank Iván Jiménez for help collecting Commelina communis material and two anonymous reviewers for comments on a previous version of the manuscript. This work was supported by a National Science Foundation grant (IOS-0616025) to LCH.
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