Molecular Biology and Evolution 19:587-596 (2002)
© 2002 Society for Molecular Biology and Evolution
Evolution of Class B Floral Homeotic Proteins: Obligate Heterodimerization Originated from Homodimerization
Max-Planck-Institut für Züchtungsforschung, Abteilung Molekulare Pflanzengenetik, Köln, Germany
The class B floral homeotic genes from the higher eudicot model systems Arabidopsis and Antirrhinum are involved in specifying the identity of petals and stamens during flower development. These genes exist in two different types termed DEF- and GLO-like genes. The proteins encoded by the class B genes are stable and functional in the cell only as heterodimeric complexes of a DEF- and a GLO-like protein. In line with this, heterodimerization is obligate for DNA binding in vitro. The genes whose products have to heterodimerize to be stable and functional are each other's closest relatives within their genomes. This suggests that the respective genes originated by gene duplication, and that heterodimerization is of relative recent origin and evolved from homodimerization. To test this hypothesis we have investigated the dimerization behavior of putative B proteins from phylogenetic informative taxa, employing electrophoretic mobility shift assays and the yeast two-hybrid system. We find that an ancestral B protein from the gymnosperm Gnetum gnemon binds DNA in a sequence-specific manner as a homodimer. Of the two types of B proteins from the monocot Lilium regale, the GLO-like protein is still able to homodimerize, whereas the DEF-like protein binds to DNA only as a heterodimeric complex with the GLO-like protein. These data suggest that heterodimerization evolved in two steps after a gene duplication that gave rise to DEF- and GLO-like genes. Heterodimerization may have originated after the gymnosperm-angiosperm split about 300 MYA but before the monocot-eudicot split 140200 MYA. Heterodimerization may have become obligate for both types of flowering plant B proteins in the eudicot lineage after the monocot-eudicot split.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
Y.-Y. Chang, N.-H. Kao, J.-Y. Li, W.-H. Hsu, Y.-L. Liang, J.-W. Wu, and C.-H. Yang Characterization of the Possible Roles for B Class MADS Box Genes in Regulation of Perianth Formation in Orchid Plant Physiology, February 1, 2010; 152(2): 837 - 853. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. F. Irish Evolution of petal identity J. Exp. Bot., July 1, 2009; 60(9): 2517 - 2527. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Melzer, W. Verelst, and G. Theissen The class E floral homeotic protein SEPALLATA3 is sufficient to loop DNA in 'floral quartet'-like complexes in vitro Nucleic Acids Res., January 1, 2009; 37(1): 144 - 157. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. C. Hileman and V. F. Irish More is better: the uses of developmental genetic data to reconstruct perianth evolution Am. J. Botany, January 1, 2009; 96(1): 83 - 95. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-K. Chen, I-C. Lin, and C.-H. Yang Functional Analysis of Three Lily (Lilium longiflorum) APETALA1-like MADS Box Genes in Regulating Floral Transition and Formation Plant Cell Physiol., May 1, 2008; 49(5): 704 - 717. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-C. Tsai, Z.-J. Pan, Y.-Y. Hsiao, M.-F. Jeng, T.-F. Wu, W.-H. Chen, and H.-H. Chen Interactions of B-class complex proteins involved in tepal development in Phalaenopsis orchid Plant Cell Physiol., May 1, 2008; 49(5): 814 - 824. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Drea, L. C. Hileman, G. de Martino, and V. F. Irish Functional analyses of genetic pathways controlling petal specification in poppy Development, December 1, 2007; 134(23): 4157 - 4166. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Piwarzyk, Y. Yang, and T. Jack Conserved C-Terminal Motifs of the Arabidopsis Proteins APETALA3 and PISTILLATA Are Dispensable for Floral Organ Identity Function Plant Physiology, December 1, 2007; 145(4): 1495 - 1505. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Theissen and R. Melzer Molecular Mechanisms Underlying Origin and Diversification of the Angiosperm Flower Ann. Bot., September 1, 2007; 100(3): 603 - 619. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Adam, S. Jouannic, F. Morcillo, J.-L. Verdeil, Y. Duval, and J. W. Tregear Determination of Flower Structure in Elaeis guineensis: Do Palms use the Same Homeotic Genes as Other Species? Ann. Bot., July 1, 2007; 100(1): 1 - 12. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. M. Kramer, L. Holappa, B. Gould, M. A. Jaramillo, D. Setnikov, and P. M. Santiago Elaboration of B Gene Function to Include the Identity of Novel Floral Organs in the Lower Eudicot Aquilegia PLANT CELL, March 1, 2007; 19(3): 750 - 766. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. S. Veron, K. Kaufmann, and E. Bornberg-Bauer Evidence of Interaction Network Evolution by Whole-Genome Duplications: A Case Study in MADS-Box Proteins Mol. Biol. Evol., March 1, 2007; 24(3): 670 - 678. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Hernandez-Hernandez, L. P. Martinez-Castilla, and E. R. Alvarez-Buylla Functional Diversification of B MADS-Box Homeotic Regulators of Flower Development: Adaptive Evolution in Protein-Protein Interaction Domains after Major Gene Duplication Events Mol. Biol. Evol., February 1, 2007; 24(2): 465 - 481. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. Kater, L. Dreni, and L. Colombo Functional conservation of MADS-box factors controlling floral organ identity in rice and Arabidopsis J. Exp. Bot., October 1, 2006; 57(13): 3433 - 3444. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Zahn, J. Leebens-Mack, C. W. dePamphilis, H. Ma, and G. Theissen To B or Not to B a Flower: The Role of DEFICIENS and GLOBOSA Orthologs in the Evolution of the Angiosperms J. Hered., May 1, 2005; 96(3): 225 - 240. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Zahn, H. Kong, J. H. Leebens-Mack, S. Kim, P. S. Soltis, L. L. Landherr, D. E. Soltis, C. W. dePamphilis, and H. Ma The Evolution of the SEPALLATA Subfamily of MADS-Box Genes: A Preangiosperm Origin With Multiple Duplications Throughout Angiosperm History Genetics, April 1, 2005; 169(4): 2209 - 2223. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. Whipple, P. Ciceri, C. M. Padilla, B. A. Ambrose, S. L. Bandong, and R. J. Schmidt Conservation of B-class floral homeotic gene function between maize and Arabidopsis Development, December 15, 2004; 131(24): 6083 - 6091. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Kim, M.-J. Yoo, V. A. Albert, J. S. Farris, P. S. Soltis, and D. E. Soltis Phylogeny and diversification of B-function MADS-box genes in angiosperms: evolutionary and functional implications of a 260-million-year-old duplication Am. J. Botany, December 1, 2004; 91(12): 2102 - 2118. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. A. Benedito, P. B. Visser, J. M. van Tuyl, G. C. Angenent, S. C. de Vries, and F. A. Krens Ectopic expression of LLAG1, an AGAMOUS homologue from lily (Lilium longiflorum Thunb.) causes floral homeotic modifications in Arabidopsis J. Exp. Bot., June 1, 2004; 55(401): 1391 - 1399. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. V. Shchennikova, O. A. Shulga, R. Immink, K. G. Skryabin, and G. C. Angenent Identification and Characterization of Four Chrysanthemum MADS-Box Genes, Belonging to the APETALA1/FRUITFULL and SEPALLATA3 Subfamilies Plant Physiology, April 1, 2004; 134(4): 1632 - 1641. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-H. Park, Y. Ishikawa, T. Ochiai, A. Kanno, and T. Kameya Two GLOBOSA-Like Genes are Expressed in Second and Third Whorls of Homochlamydeous Flowers in Asparagus officinalis L. Plant Cell Physiol., March 15, 2004; 45(3): 325 - 332. [Abstract] [Full Text] [PDF] |
||||
![]() |
T.-Y. Tzeng, H.-C. Liu, and C.-H. Yang The C-terminal Sequence of LMADS1 Is Essential for the Formation of Homodimers for B Function Proteins J. Biol. Chem., March 12, 2004; 279(11): 10747 - 10755. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. M. Stellari, M. A. Jaramillo, and E. M. Kramer Evolution of the APETALA3 and PISTILLATA Lineages of MADS-Box-Containing Genes in the Basal Angiosperms Mol. Biol. Evol., March 1, 2004; 21(3): 506 - 519. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Tsuchisaka and A. Theologis Heterodimeric interactions among the 1-amino-cyclopropane-1-carboxylate synthase polypeptides encoded by the Arabidopsis gene family PNAS, February 24, 2004; 101(8): 2275 - 2280. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Vandenbussche, G. Theissen, Y. Van de Peer, and T. Gerats Structural diversification and neo-functionalization during floral MADS-box gene evolution by C-terminal frameshift mutations Nucleic Acids Res., August 1, 2003; 31(15): 4401 - 4409. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. S. Lamb and V. F. Irish Functional divergence within the APETALA3/PISTILLATA floral homeotic gene lineages PNAS, May 27, 2003; 100(11): 6558 - 6563. [Abstract] [Full Text] [PDF] |
||||












