Literature DB >> 12244239

Homeotic Transformation of Ovules into Carpel-like Structures in Arabidopsis.

Z. Modrusan1, L. Reiser, K. A. Feldmann, R. L. Fischer, G. W. Haughn.   

Abstract

Ovules are specialized reproductive organs that develop within the carpels of higher plants. In Arabidopsis, mutations in two genes, BELL1 (BEL1) and APETALA2 (AP2), disrupt ovule development. In Bel1 ovules, the inner integument fails to form, the outer integument develops abnormally, and the embryo sac arrests at a late stage of megagametogenesis. During later stages of ovule development, cells of the outer integument of a Bel1 ovule sometimes develop into a carpel-like structure with stigmatic papillae and second-order ovules. The frequency of carpel-like structures was highest when plants were grown under conditions that normally induced flowering and was correlated with ectopic expression in the ovule of AGAMOUS (AG), an organ-identity gene required for carpel formation. Together, these results suggested that BEL1 negatively regulates AG late in ovule development. Likewise, mutants homozygous for the strong AP2 allele ap2-6 sometimes displayed structures with carpel-like features in place of ovules. However, such abnormal Ap2 ovules are much less ovulelike in morphology and form earlier than the Bel1 carpel-like structures. Because one role of the AP2 gene is to negatively regulate AG expression early in flower development, it is possible that AP2 works in a similar manner in the ovule. A novel ovule phenotype observed in Bel1/Ap2-6 double mutants suggested that BEL1 and AP2 genes function independently during ovule development.

Entities:  

Year:  1994        PMID: 12244239      PMCID: PMC160437          DOI: 10.1105/tpc.6.3.333

Source DB:  PubMed          Journal:  Plant Cell        ISSN: 1040-4651            Impact factor:   11.277


  15 in total

1.  Negative regulation of the Arabidopsis homeotic gene AGAMOUS by the APETALA2 product.

Authors:  G N Drews; J L Bowman; E M Meyerowitz
Journal:  Cell       Date:  1991-06-14       Impact factor: 41.582

2.  Ovule Development in Wild-Type Arabidopsis and Two Female-Sterile Mutants.

Authors:  K. Robinson-Beers; R. E. Pruitt; C. S. Gasser
Journal:  Plant Cell       Date:  1992-10       Impact factor: 11.277

3.  Selection-expression plasmid vectors for use in genetic transformation of higher plants.

Authors:  J Velten; J Schell
Journal:  Nucleic Acids Res       Date:  1985-10-11       Impact factor: 16.971

4.  LINKAGE-1: a PASCAL computer program for the detection and analysis of genetic linkage.

Authors:  K A Suiter; J F Wendel; J S Case
Journal:  J Hered       Date:  1983 May-Jun       Impact factor: 2.645

5.  Early flower development in Arabidopsis.

Authors:  D R Smyth; J L Bowman; E M Meyerowitz
Journal:  Plant Cell       Date:  1990-08       Impact factor: 11.277

6.  Manipulation of flower structure in transgenic tobacco.

Authors:  M A Mandel; J L Bowman; S A Kempin; H Ma; E M Meyerowitz; M F Yanofsky
Journal:  Cell       Date:  1992-10-02       Impact factor: 41.582

7.  Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum.

Authors:  D Bradley; R Carpenter; H Sommer; N Hartley; E Coen
Journal:  Cell       Date:  1993-01-15       Impact factor: 41.582

8.  The FLO10 Gene Product Regulates the Expression Domain of Homeotic Genes AP3 and PI in Arabidopsis Flowers.

Authors:  E. A. Schultz; F. B. Pickett; G. W. Haughn
Journal:  Plant Cell       Date:  1991-11       Impact factor: 11.277

9.  AP2 Gene Determines the Identity of Perianth Organs in Flowers of Arabidopsis thaliana.

Authors:  L. Kunst; J. E. Klenz; J. Martinez-Zapater; G. W. Haughn
Journal:  Plant Cell       Date:  1989-12       Impact factor: 11.277

10.  Bracteomania, an inflorescence anomaly, is caused by the loss of function of the MADS-box gene squamosa in Antirrhinum majus.

Authors:  P Huijser; J Klein; W E Lönnig; H Meijer; H Saedler; H Sommer
Journal:  EMBO J       Date:  1992-04       Impact factor: 11.598

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  85 in total

1.  Isolation and characterization of mutants defective in seed coat mucilage secretory cell development in Arabidopsis.

Authors:  T L Western; J Burn; W L Tan; D J Skinner; L Martin-McCaffrey; B A Moffatt; G W Haughn
Journal:  Plant Physiol       Date:  2001-11       Impact factor: 8.340

2.  Separation of genetic functions controlling organ identity in flowers.

Authors:  Emma Keck; Paula McSteen; Rosemary Carpenter; Enrico Coen
Journal:  EMBO J       Date:  2003-03-03       Impact factor: 11.598

3.  SHORT INTEGUMENTS 2 promotes growth during Arabidopsis reproductive development.

Authors:  J Broadhvest; S C Baker; C S Gasser
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

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

5.  The phenotype of Arabidopsis ovule mutants mimics the morphology of primitive seed plants.

Authors:  Sung Ok Park; Soon Hwang; Bernard A Hauser
Journal:  Proc Biol Sci       Date:  2004-02-07       Impact factor: 5.349

6.  Molecular mapping of four ovule lethal mutants in soybean.

Authors:  K K Kato; R G Palmer
Journal:  Theor Appl Genet       Date:  2003-11-11       Impact factor: 5.699

Review 7.  Regulation of protein function by 'microProteins'.

Authors:  Annica-Carolin Staudt; Stephan Wenkel
Journal:  EMBO Rep       Date:  2010-12-10       Impact factor: 8.807

8.  Flower development.

Authors:  Elena R Alvarez-Buylla; Mariana Benítez; Adriana Corvera-Poiré; Alvaro Chaos Cador; Stefan de Folter; Alicia Gamboa de Buen; Adriana Garay-Arroyo; Berenice García-Ponce; Fabiola Jaimes-Miranda; Rigoberto V Pérez-Ruiz; Alma Piñeyro-Nelson; Yara E Sánchez-Corrales
Journal:  Arabidopsis Book       Date:  2010-03-23

9.  Arabidopsis TSO1 regulates directional processes in cells during floral organogenesis.

Authors:  B A Hauser; J M Villanueva; C S Gasser
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

10.  The Arabidopsis BEL1-LIKE HOMEODOMAIN proteins SAW1 and SAW2 act redundantly to regulate KNOX expression spatially in leaf margins.

Authors:  Ravi Kumar; Kumuda Kushalappa; Dietmute Godt; Mark S Pidkowich; Sandro Pastorelli; Shelley R Hepworth; George W Haughn
Journal:  Plant Cell       Date:  2007-09-14       Impact factor: 11.277

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