Literature DB >> 11231153

Conversion of leaves into petals in Arabidopsis.

S Pelaz1, R Tapia-López, E R Alvarez-Buylla, M F Yanofsky.   

Abstract

More than 200 years ago, Goethe proposed that each of the distinct flower organs represents a modified leaf [1]. Support for this hypothesis has come from genetic studies, which have identified genes required for flower organ identity. These genes have been incorporated into the widely accepted ABC model of flower organ identity, a model that appears generally applicable to distantly related eudicots as well as monocot plants. Strikingly, triple mutants lacking the ABC activities produce leaves in place of flower organs, and this finding demonstrates that these genes are required for floral organ identity [2]. However, the ABC genes are not sufficient for floral organ identity since ectopic expression of these genes failed to convert vegetative leaves into flower organs. This finding suggests that one or more additional factors are required [3, 4]. We have recently shown that SEPALLATA (SEP) represents a new class of floral organ identity genes since the loss of SEP activity results in all flower organs developing as sepals [5]. Here we show that the combined action of the SEP genes, together with the A and B genes, is sufficient to convert leaves into petals.

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Year:  2001        PMID: 11231153     DOI: 10.1016/s0960-9822(01)00024-0

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  90 in total

1.  Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana).

Authors:  Akira Kanno; Hiroshi Saeki; Toshiaki Kameya; Heinz Saedler; Günter Theissen
Journal:  Plant Mol Biol       Date:  2003-07       Impact factor: 4.076

2.  An antirrhinum ternary complex factor specifically interacts with C-function and SEPALLATA-like MADS-box factors.

Authors:  Barry Causier; Holly Cook; Brendan Davies
Journal:  Plant Mol Biol       Date:  2003-07       Impact factor: 4.076

3.  Functional analysis of the rice AP3 homologue OsMADS16 by RNA interference.

Authors:  Han Xiao; Yun Wang; Daofeng Liu; Wemming Wang; Xiaobing Li; Xianfeng Zhao; Jichen Xu; Wenxue Zhai; Lihuang Zhu
Journal:  Plant Mol Biol       Date:  2003-07       Impact factor: 4.076

Review 4.  Regulation of ovule development.

Authors:  Debra J Skinner; Theresa A Hill; Charles S Gasser
Journal:  Plant Cell       Date:  2004-05-06       Impact factor: 11.277

Review 5.  Molecular and genetic mechanisms of floral control.

Authors:  Thomas Jack
Journal:  Plant Cell       Date:  2004-03-12       Impact factor: 11.277

6.  Fruit development in Arabidopsis.

Authors:  Adrienne H K Roeder; Martin F Yanofsky
Journal:  Arabidopsis Book       Date:  2006-02-22

Review 7.  Distinct and dynamic auxin activities during reproductive development.

Authors:  Eva Sundberg; Lars Østergaard
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-10-14       Impact factor: 10.005

8.  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

9.  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

10.  A gene regulatory network model for cell-fate determination during Arabidopsis thaliana flower development that is robust and recovers experimental gene expression profiles.

Authors:  Carlos Espinosa-Soto; Pablo Padilla-Longoria; Elena R Alvarez-Buylla
Journal:  Plant Cell       Date:  2004-10-14       Impact factor: 11.277

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