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Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant
BACKGROUND: Male sterility is an efficient trait for hybrid seed production and germplasm innovation. Until now, most studies on male sterility were on cytoplasmic and recessive genic sterility, with few on dominant genic male sterility, especially in cotton, due to lack of such mutant. RESULTS: We...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333317/ https://www.ncbi.nlm.nih.gov/pubmed/32620078 http://dx.doi.org/10.1186/s12870-020-02522-0 |
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author | Cheng, Xin-Qi Zhang, Xin-Yu Xue, Fei Zhu, Shou-Hong Li, Yan-Jun Zhu, Qian-Hao Liu, Feng Sun, Jie |
author_facet | Cheng, Xin-Qi Zhang, Xin-Yu Xue, Fei Zhu, Shou-Hong Li, Yan-Jun Zhu, Qian-Hao Liu, Feng Sun, Jie |
author_sort | Cheng, Xin-Qi |
collection | PubMed |
description | BACKGROUND: Male sterility is an efficient trait for hybrid seed production and germplasm innovation. Until now, most studies on male sterility were on cytoplasmic and recessive genic sterility, with few on dominant genic male sterility, especially in cotton, due to lack of such mutant. RESULTS: We discovered a natural male sterile (MS) Sea Island cotton (G. barbadense) mutant. Genetic analysis showed the mutation was caused by a dominant mutation in a single nuclear gene. Comparative cytological observation of anther sections from MS and wild-type (WT) uncovered cellular differences in anther at and after the tetrad stage of pollen mother cells (PMC). In the MS anthers, the outer wall of pollen grains was free of spinules, the tapetum was vacuolated and showed delayed degradation, consequently, no functional pollen grains. Comparison of transcriptomes from meiosis, tetrad, mononuclear and binuclear pollen, and pollen maturation stages identified 13,783 non-redundant differentially expressed genes (DEGs) between MS and WT. Based on the number of DEGs, analyses of enriched GO terms and KEGG pathways, it was evident that significant transcriptomic changes occurred at and after the tetrad stage, consistent with cytological observation, and that the major differences were on metabolism of starch, sucrose, ascorbate, aldarate, alanine, aspartate and glutamate, and biosynthesis of cutin, suberine and wax. WGCNA analysis identified five modules containing 920 genes highly related to anther development, especially the greenyellow module with 54 genes that was highly associated with PMC meiosis and tetrad formation. A NAC transcription factor (Gh_D11G2469) was identified as a hub gene for this module, which warrants further functional characterization. CONCLUSIONS: We demonstrated that the MS trait was controlled by a single dominant nuclear gene and caused by delayed tapetum degradation at the tetrad stage. Comparative transcriptome analysis and gene network construction identified DEGs, enriched GO terms and metabolic pathways, and hub genes potentially associated with anther development and the MS trait. These results contribute to our understanding of dominant genic male sterility (DGMS) and provided source for innovation of cotton germplasm. |
format | Online Article Text |
id | pubmed-7333317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73333172020-07-06 Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant Cheng, Xin-Qi Zhang, Xin-Yu Xue, Fei Zhu, Shou-Hong Li, Yan-Jun Zhu, Qian-Hao Liu, Feng Sun, Jie BMC Plant Biol Research Article BACKGROUND: Male sterility is an efficient trait for hybrid seed production and germplasm innovation. Until now, most studies on male sterility were on cytoplasmic and recessive genic sterility, with few on dominant genic male sterility, especially in cotton, due to lack of such mutant. RESULTS: We discovered a natural male sterile (MS) Sea Island cotton (G. barbadense) mutant. Genetic analysis showed the mutation was caused by a dominant mutation in a single nuclear gene. Comparative cytological observation of anther sections from MS and wild-type (WT) uncovered cellular differences in anther at and after the tetrad stage of pollen mother cells (PMC). In the MS anthers, the outer wall of pollen grains was free of spinules, the tapetum was vacuolated and showed delayed degradation, consequently, no functional pollen grains. Comparison of transcriptomes from meiosis, tetrad, mononuclear and binuclear pollen, and pollen maturation stages identified 13,783 non-redundant differentially expressed genes (DEGs) between MS and WT. Based on the number of DEGs, analyses of enriched GO terms and KEGG pathways, it was evident that significant transcriptomic changes occurred at and after the tetrad stage, consistent with cytological observation, and that the major differences were on metabolism of starch, sucrose, ascorbate, aldarate, alanine, aspartate and glutamate, and biosynthesis of cutin, suberine and wax. WGCNA analysis identified five modules containing 920 genes highly related to anther development, especially the greenyellow module with 54 genes that was highly associated with PMC meiosis and tetrad formation. A NAC transcription factor (Gh_D11G2469) was identified as a hub gene for this module, which warrants further functional characterization. CONCLUSIONS: We demonstrated that the MS trait was controlled by a single dominant nuclear gene and caused by delayed tapetum degradation at the tetrad stage. Comparative transcriptome analysis and gene network construction identified DEGs, enriched GO terms and metabolic pathways, and hub genes potentially associated with anther development and the MS trait. These results contribute to our understanding of dominant genic male sterility (DGMS) and provided source for innovation of cotton germplasm. BioMed Central 2020-07-03 /pmc/articles/PMC7333317/ /pubmed/32620078 http://dx.doi.org/10.1186/s12870-020-02522-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Cheng, Xin-Qi Zhang, Xin-Yu Xue, Fei Zhu, Shou-Hong Li, Yan-Jun Zhu, Qian-Hao Liu, Feng Sun, Jie Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title | Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title_full | Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title_fullStr | Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title_full_unstemmed | Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title_short | Characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
title_sort | characterization and transcriptome analysis of a dominant genic male sterile cotton mutant |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333317/ https://www.ncbi.nlm.nih.gov/pubmed/32620078 http://dx.doi.org/10.1186/s12870-020-02522-0 |
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