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The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm

Many homeotic MADS-box genes have been identified as controllers of the floral transition and floral development. However, information regarding B(sister) (B(s))-function genes in monocots is still limited. Here, we describe the functional characterization of a B(s)-group MADS-box gene FEMALE-STERIL...

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Autores principales: Lee, Dong Sun, Chen, Li Juan, Li, Cheng Yun, Liu, Yongsheng, Tan, Xue Lin, Lu, Bao-Rong, Li, Juan, Gan, Shu Xian, Kang, Sang Gu, Suh, Hak Soo, Zhu, Youyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602522/
https://www.ncbi.nlm.nih.gov/pubmed/23527017
http://dx.doi.org/10.1371/journal.pone.0058748
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author Lee, Dong Sun
Chen, Li Juan
Li, Cheng Yun
Liu, Yongsheng
Tan, Xue Lin
Lu, Bao-Rong
Li, Juan
Gan, Shu Xian
Kang, Sang Gu
Suh, Hak Soo
Zhu, Youyong
author_facet Lee, Dong Sun
Chen, Li Juan
Li, Cheng Yun
Liu, Yongsheng
Tan, Xue Lin
Lu, Bao-Rong
Li, Juan
Gan, Shu Xian
Kang, Sang Gu
Suh, Hak Soo
Zhu, Youyong
author_sort Lee, Dong Sun
collection PubMed
description Many homeotic MADS-box genes have been identified as controllers of the floral transition and floral development. However, information regarding B(sister) (B(s))-function genes in monocots is still limited. Here, we describe the functional characterization of a B(s)-group MADS-box gene FEMALE-STERILE (FST), whose frame-shift mutation (fst) results in abnormal ovules and the complete abortion of zygotic embryos and endosperms in rice. Anatomical analysis showed that the defective development in the fst mutant exclusively occurred in sporophytic tissues including integuments, fertilized proembryos and endosperms. Analyses of the spatio-temporal expression pattern revealed that the prominent FST gene products accumulated in the inner integument, nucellar cell of the micropylar side, apical and base of the proembryos and free endosperm nuclei. Microarray and gene ontology analysis unraveled substantial changes in the expression level of many genes in the fst mutant ovules and seeds, with a subset of genes involved in several developmental and hormonal pathways appearing to be down-regulated. Using both forward and reverse genetics approaches, we demonstrated that rice FST plays indispensable roles and multiple functions during ovule and early seed development. These findings support a novel function for the B(s)-group MADS-box genes in plants.
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spelling pubmed-36025222013-03-22 The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm Lee, Dong Sun Chen, Li Juan Li, Cheng Yun Liu, Yongsheng Tan, Xue Lin Lu, Bao-Rong Li, Juan Gan, Shu Xian Kang, Sang Gu Suh, Hak Soo Zhu, Youyong PLoS One Research Article Many homeotic MADS-box genes have been identified as controllers of the floral transition and floral development. However, information regarding B(sister) (B(s))-function genes in monocots is still limited. Here, we describe the functional characterization of a B(s)-group MADS-box gene FEMALE-STERILE (FST), whose frame-shift mutation (fst) results in abnormal ovules and the complete abortion of zygotic embryos and endosperms in rice. Anatomical analysis showed that the defective development in the fst mutant exclusively occurred in sporophytic tissues including integuments, fertilized proembryos and endosperms. Analyses of the spatio-temporal expression pattern revealed that the prominent FST gene products accumulated in the inner integument, nucellar cell of the micropylar side, apical and base of the proembryos and free endosperm nuclei. Microarray and gene ontology analysis unraveled substantial changes in the expression level of many genes in the fst mutant ovules and seeds, with a subset of genes involved in several developmental and hormonal pathways appearing to be down-regulated. Using both forward and reverse genetics approaches, we demonstrated that rice FST plays indispensable roles and multiple functions during ovule and early seed development. These findings support a novel function for the B(s)-group MADS-box genes in plants. Public Library of Science 2013-03-19 /pmc/articles/PMC3602522/ /pubmed/23527017 http://dx.doi.org/10.1371/journal.pone.0058748 Text en © 2013 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Dong Sun
Chen, Li Juan
Li, Cheng Yun
Liu, Yongsheng
Tan, Xue Lin
Lu, Bao-Rong
Li, Juan
Gan, Shu Xian
Kang, Sang Gu
Suh, Hak Soo
Zhu, Youyong
The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title_full The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title_fullStr The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title_full_unstemmed The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title_short The B(sister) MADS Gene FST Determines Ovule Patterning and Development of the Zygotic Embryo and Endosperm
title_sort b(sister) mads gene fst determines ovule patterning and development of the zygotic embryo and endosperm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602522/
https://www.ncbi.nlm.nih.gov/pubmed/23527017
http://dx.doi.org/10.1371/journal.pone.0058748
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