Literature DB >> 15687268

The evolution of the SEPALLATA subfamily of MADS-box genes: a preangiosperm origin with multiple duplications throughout angiosperm history.

Laura M Zahn1, Hongzhi Kong, James H Leebens-Mack, Sangtae Kim, Pamela S Soltis, Lena L Landherr, Douglas E Soltis, Claude W Depamphilis, Hong Ma.   

Abstract

Members of the SEPALLATA (SEP) MADS-box subfamily are required for specifying the "floral state" by contributing to floral organ and meristem identity. SEP genes have not been detected in gymnosperms and seem to have originated since the lineage leading to extant angiosperms diverged from extant gymnosperms. Therefore, both functional and evolutionary studies suggest that SEP genes may have been critical for the origin of the flower. To gain insights into the evolution of SEP genes, we isolated nine genes from plants that occupy phylogenetically important positions. Phylogenetic analyses of SEP sequences show that several gene duplications occurred during the evolution of this subfamily, providing potential opportunities for functional divergence. The first duplication occurred prior to the origin of the extant angiosperms, resulting in the AGL2/3/4 and AGL9 clades. Subsequent duplications occurred within these clades in the eudicots and monocots. The timing of the first SEP duplication approximately coincides with duplications in the DEFICIENS/GLOBOSA and AGAMOUS MADS-box subfamilies, which may have resulted from either a proposed genome-wide duplication in the ancestor of extant angiosperms or multiple independent duplication events. Regardless of the mechanism of gene duplication, these pairs of duplicate transcription factors provided new possibilities of genetic interactions that may have been important in the origin of the flower.

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Year:  2005        PMID: 15687268      PMCID: PMC1449606          DOI: 10.1534/genetics.104.037770

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  87 in total

1.  The root of angiosperm phylogeny inferred from duplicate phytochrome genes.

Authors:  S Mathews; M J Donoghue
Journal:  Science       Date:  1999-10-29       Impact factor: 47.728

2.  Plant biology. Floral quartets.

Authors:  G Theissen; H Saedler
Journal:  Nature       Date:  2001-01-25       Impact factor: 49.962

3.  Independent and combined analyses of sequences from all three genomic compartments converge on the root of flowering plant phylogeny.

Authors:  T J Barkman; G Chenery; J R McNeal; J Lyons-Weiler; W J Ellisens; G Moore; A D Wolfe; C W dePamphilis
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

Review 4.  Missing links: the genetic architecture of flowers [correction of flower] and floral diversification.

Authors:  Douglas E Soltis; Pamela S Soltis; Victor A Albert; David G Oppenheimer; Claude W dePamphilis; Hong Ma; Michael W Frohlich; Günter Theissen
Journal:  Trends Plant Sci       Date:  2002-01       Impact factor: 18.313

Review 5.  Preservation of duplicate genes by complementary, degenerative mutations.

Authors:  A Force; M Lynch; F B Pickett; A Amores; Y L Yan; J Postlethwait
Journal:  Genetics       Date:  1999-04       Impact factor: 4.562

6.  Adaptive evolution in the Arabidopsis MADS-box gene family inferred from its complete resolved phylogeny.

Authors:  León Patricio Martinez-Castilla; Elena R Alvarez-Buylla
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-03       Impact factor: 11.205

7.  Ternary complex formation between the MADS-box proteins SQUAMOSA, DEFICIENS and GLOBOSA is involved in the control of floral architecture in Antirrhinum majus.

Authors:  M Egea-Cortines; H Saedler; H Sommer
Journal:  EMBO J       Date:  1999-10-01       Impact factor: 11.598

8.  Analysis of MADS box protein-protein interactions in living plant cells.

Authors:  Richard G H Immink; Theodorus W J Gadella; Silvia Ferrario; Marco Busscher; Gerco C Angenent
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-19       Impact factor: 11.205

9.  MADS-box protein complexes control carpel and ovule development in Arabidopsis.

Authors:  Rebecca Favaro; Anusak Pinyopich; Raffaella Battaglia; Maarten Kooiker; Lorenzo Borghi; Gary Ditta; Martin F Yanofsky; Martin M Kater; Lucia Colombo
Journal:  Plant Cell       Date:  2003-10-10       Impact factor: 11.277

10.  Functional divergence within the APETALA3/PISTILLATA floral homeotic gene lineages.

Authors:  Rebecca S Lamb; Vivian F Irish
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-13       Impact factor: 11.205

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  118 in total

1.  Poppy APETALA1/FRUITFULL orthologs control flowering time, branching, perianth identity, and fruit development.

Authors:  Natalia Pabón-Mora; Barbara A Ambrose; Amy Litt
Journal:  Plant Physiol       Date:  2012-01-27       Impact factor: 8.340

2.  Phylogenetic and evolutionary analysis of A-, B-, C- and E-class MADS-box genes in the basal eudicot Platanus acerifolia.

Authors:  Zhineng Li; Jiaqi Zhang; Guofeng Liu; Xiaomei Li; Chen Lu; Junwei Zhang; Manzhu Bao
Journal:  J Plant Res       Date:  2011-11-09       Impact factor: 2.629

3.  Genome-wide expression profiling and identification of gene activities during early flower development in Arabidopsis.

Authors:  Xiaohong Zhang; Baomin Feng; Qing Zhang; Diya Zhang; Naomi Altman; Hong Ma
Journal:  Plant Mol Biol       Date:  2005-06       Impact factor: 4.076

4.  Reconstructing the evolutionary history of paralogous APETALA1/FRUITFULL-like genes in grasses (Poaceae).

Authors:  Jill C Preston; Elizabeth A Kellogg
Journal:  Genetics       Date:  2006-07-02       Impact factor: 4.562

5.  Phylogenetic analysis of the "ECE" (CYC/TB1) clade reveals duplications predating the core eudicots.

Authors:  Dianella G Howarth; Michael J Donoghue
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-05       Impact factor: 11.205

Review 6.  Molecular mechanisms underlying origin and diversification of the angiosperm flower.

Authors:  Guenter Theissen; Rainer Melzer
Journal:  Ann Bot       Date:  2007-07-31       Impact factor: 4.357

7.  MADS box genes in oil palm (Elaeis guineensis): patterns in the evolution of the SQUAMOSA, DEFICIENS, GLOBOSA, AGAMOUS, and SEPALLATA subfamilies.

Authors:  Hélène Adam; Stefan Jouannic; Fabienne Morcillo; Frédérique Richaud; Yves Duval; James W Tregear
Journal:  J Mol Evol       Date:  2005-11-30       Impact factor: 2.395

Review 8.  The ABC model and its applicability to basal angiosperms.

Authors:  Douglas E Soltis; André S Chanderbali; Sangtae Kim; Matyas Buzgo; Pamela S Soltis
Journal:  Ann Bot       Date:  2007-07-06       Impact factor: 4.357

9.  Loss of LOFSEP Transcription Factor Function Converts Spikelet to Leaf-Like Structures in Rice.

Authors:  Di Wu; Wanqi Liang; Wanwan Zhu; Mingjiao Chen; Cristina Ferrándiz; Rachel A Burton; Ludovico Dreni; Dabing Zhang
Journal:  Plant Physiol       Date:  2017-12-07       Impact factor: 8.340

10.  APETALA2 negatively regulates multiple floral organ identity genes in Arabidopsis by recruiting the co-repressor TOPLESS and the histone deacetylase HDA19.

Authors:  Naden T Krogan; Kendra Hogan; Jeff A Long
Journal:  Development       Date:  2012-10-03       Impact factor: 6.868

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