Literature DB >> 11179662

Characterization of three GLOBOSA-like MADS-box genes from maize: evidence for ancient paralogy in one class of floral homeotic B-function genes of grasses.

T Münster1, L U Wingen, W Faigl, S Werth, H Saedler, G Theissen.   

Abstract

Floral homeotic B-function genes are involved in specifying the identity of petals and stamens during flower development in higher eudicotyledonous plants. Monocotyledonous plants belonging to the grass family (Poaceae) have very similar B-function genes, except that these genes specify lodicules rather than petals. All B-function genes known so far are members of the MADS-box gene family encoding transcription factors. In some eudicot model systems such as Arabidopsis and Antirrhinum, the B-function is provided by heterodimeric protein complexes encoded by one DEF- and one GLO-like gene. In several different lineages of flowering plant species, however, more than one DEF- or GLO-like gene is found. A known example is the monocot model system rice, which contains two GLO-like genes, termed OSMADS2 and OSMADS4. Duplications of floral homeotic genes may have played a critical role in the diversification of floral homeotic functions and thus the evolution of flowers. In order to date the gene duplication event that gave rise to these two genes, we cloned cDNAs of three different GLO-like genes from maize, a distant relative of rice within the Poaceae family. Phylogeny reconstructions and chromosomal mapping indicate that one of these genes, named ZMM16, is orthologous to OSMADS2, and that the other two, ZMM18 and ZMM29, are probably orthologous to OSMADS4. The gene duplication which gave rise to OSMADS2- and OSMADS4-like genes occurred probably after the split of the lineages that resulted in extant Liliaceae and Poaceae, but before the separation of the lineages that gave rise to extant maize and rice about 50 MYA. Northern and in situ hybridization studies demonstrated that the maize genes are expressed in lodicules, stamens and carpels throughout spikelet development in male and female inflorescences. The GLO-like genes from rice have very similar patterns of mRNA accumulation. In addition, ZMM16 shows also weak expression in vegetative organs. Conservation of the expression in lodicules and stamens is in perfect agreement with a floral homeotic B-function of the GLO-like genes in grasses. The conserved expression in carpels is discussed. Moreover, circumstantial evidence for a functional diversification of GLO-like genes in grasses is provided.

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Year:  2001        PMID: 11179662     DOI: 10.1016/s0378-1119(00)00556-4

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  39 in total

1.  Double-stranded RNA interference of a rice PI/GLO paralog, OsMADS2, uncovers its second-whorl-specific function in floral organ patterning.

Authors:  Kalika Prasad; Usha Vijayraghavan
Journal:  Genetics       Date:  2003-12       Impact factor: 4.562

2.  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

3.  Morphological alterations by ectopic expression of the rice OsMADS4 gene in tobacco plants.

Authors:  Hong-Gyu Kang; Gynheung An
Journal:  Plant Cell Rep       Date:  2005-02-10       Impact factor: 4.570

4.  Conservation of B class gene expression in the second whorl of a basal grass and outgroups links the origin of lodicules and petals.

Authors:  Clinton J Whipple; Michael J Zanis; Elizabeth A Kellogg; Robert J Schmidt
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-08       Impact factor: 11.205

5.  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

6.  A shotgun phosphoproteomics analysis of embryos in germinated maize seeds.

Authors:  Tian-Cong Lu; Ling-Bo Meng; Chuan-Ping Yang; Gui-Feng Liu; Guan-Jun Liu; Wei Ma; Bai-Chen Wang
Journal:  Planta       Date:  2008-08-23       Impact factor: 4.116

7.  Gain of function mutation in tobacco MADS box promoter switch on the expression of flowering class B genes converting sepals to petals.

Authors:  Monika Mahajan; Sudesh Kumar Yadav
Journal:  Mol Biol Rep       Date:  2013-12-22       Impact factor: 2.316

8.  B-class MADS-box genes in trioecious papaya: two paleoAP3 paralogs, CpTM6-1 and CpTM6-2, and a PI ortholog CpPI.

Authors:  Christine M Ackerman; Qingyi Yu; Sangtae Kim; Robert E Paull; Paul H Moore; Ray Ming
Journal:  Planta       Date:  2007-11-06       Impact factor: 4.116

9.  Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid.

Authors:  Yu-Yun Chang; Nai-Hsuan Kao; Jen-Ying Li; Wei-Han Hsu; Yu-Ling Liang; Jia-Wei Wu; Chang-Hsien Yang
Journal:  Plant Physiol       Date:  2009-12-16       Impact factor: 8.340

10.  Pistillody is caused by alterations to the class-B MADS-box gene expression pattern in alloplasmic wheats.

Authors:  Eriko Hama; Shigeo Takumi; Yasunari Ogihara; Koji Murai
Journal:  Planta       Date:  2003-12-02       Impact factor: 4.116

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