Functional divergence within the APETALA3/PISTILLATA floral homeotic gene lineages

被引:179
作者
Lamb, RS
Irish, VF
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Ecol & Evolutionary Biol, New Haven, CT 06520 USA
关键词
D O I
10.1073/pnas.0631708100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Changes in homeotic gene expression patterns or in the functions of the encoded proteins are thought to play a prominent role in the evolution of new morphologies. The floral homeotic APETALA3 (AP3) and PISTILLATA (PI) genes encode MAIDS domain-containing transcription factors required to specify petal and stamen identities in Arabidopsis. We have previously shown that perianth expression of AP3 and PI homologs varies in different groups of angiosperms with diverse floral structures, suggesting that changes in expression may contribute to changing morphology. We have investigated the possibility that changes in the functions of the encoded gene products may also have played a role in the evolution of different floral morphologies. AP3 and PI are members of paralogous gene lineages and share extensive similarity along the length of the protein products. Genes within these lineages encode products with characteristic C-terminal motifs that we show are critical for functional specificity. In particular, the C terminus of AP3 is sufficient to confer AP3 functionality on the heterologous PI protein. Furthermore, we have shown that the evolution of the divergent AP3 C-terminal domain in the core eudicots is correlated with the acquisition of a role in specifying perianth structures. These results suggest that divergence in these sequence motifs has contributed to the evolution of distinct functions for these floral homeotic gene products.
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页码:6558 / 6563
页数:6
相关论文
共 60 条
[1]   Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots [J].
Ambrose, BA ;
Lerner, DR ;
Ciceri, P ;
Padilla, CM ;
Yanofsky, MF ;
Schmidt, RJ .
MOLECULAR CELL, 2000, 5 (03) :569-579
[2]   THE CAULIFLOWER MOSAIC VIRUS-35S PROMOTER - COMBINATORIAL REGULATION OF TRANSCRIPTION IN PLANTS [J].
BENFEY, PN ;
CHUA, NH .
SCIENCE, 1990, 250 (4983) :959-966
[3]   GENES DIRECTING FLOWER DEVELOPMENT IN ARABIDOPSIS [J].
BOWMAN, JL ;
SMYTH, DR ;
MEYEROWITZ, EM .
PLANT CELL, 1989, 1 (01) :37-52
[4]   Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana [J].
Clough, SJ ;
Bent, AF .
PLANT JOURNAL, 1998, 16 (06) :735-743
[5]  
DRINNAN AN, 1994, EARLY EVOLUTION FLOW, P93
[6]   Ternary complex formation between the MADS-box proteins SQUAMOSA, DEFICIENS and GLOBOSA is involved in the control of floral architecture in Antirrhinum majus [J].
Egea-Cortines, M ;
Saedler, H ;
Sommer, H .
EMBO JOURNAL, 1999, 18 (19) :5370-5379
[7]   FLORAL STRUCTURE AND EVOLUTION OF PRIMITIVE ANGIOSPERMS - RECENT ADVANCES [J].
ENDRESS, PK .
PLANT SYSTEMATICS AND EVOLUTION, 1994, 192 (1-2) :79-97
[8]   Fossil evidence of water lilies (Nymphaeales) in the Early Cretaceous [J].
Friis, EM ;
Pedersen, KR ;
Crane, PR .
NATURE, 2001, 410 (6826) :357-360
[9]   Evolution of a transcriptional repression domain in an insect Hox protein [J].
Galant, R ;
Carroll, SB .
NATURE, 2002, 415 (6874) :910-913
[10]   FUNCTION AND REGULATION OF THE ARABIDOPSIS FLORAL HOMEOTIC GENE PISTILLATA [J].
GOTO, K ;
MEYEROWITZ, EM .
GENES & DEVELOPMENT, 1994, 8 (13) :1548-1560