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Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica

BACKGROUND: The phenomenon of male sterility widely occurs in Prunus sibirica and has a serious negative impact on yield. We identified the key stage and cause of male sterility and found differentially expressed genes related to male sterility in Prunus sibirica, and we analyzed the expression patt...

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Autores principales: Chen, Jianhua, Xu, Hao, Zhang, Jian, Dong, Shengjun, Liu, Quangang, Wang, Ruoxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541319/
https://www.ncbi.nlm.nih.gov/pubmed/34722001
http://dx.doi.org/10.7717/peerj.12349
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author Chen, Jianhua
Xu, Hao
Zhang, Jian
Dong, Shengjun
Liu, Quangang
Wang, Ruoxi
author_facet Chen, Jianhua
Xu, Hao
Zhang, Jian
Dong, Shengjun
Liu, Quangang
Wang, Ruoxi
author_sort Chen, Jianhua
collection PubMed
description BACKGROUND: The phenomenon of male sterility widely occurs in Prunus sibirica and has a serious negative impact on yield. We identified the key stage and cause of male sterility and found differentially expressed genes related to male sterility in Prunus sibirica, and we analyzed the expression pattern of these genes. This work aimed to provide valuable reference and theoretical basis for the study of reproductive development and the mechanisms of male sterility in Prunus sibirica. METHOD: The microstructures of male sterile flower buds and male fertile flower buds were observed by paraffin section. Transcriptome sequencing was used to screen genes related to male sterility in Prunus sibirica. Quantitative real-time PCR analysis was performed to verify the transcriptome data. RESULTS: Anther development was divided into the sporogenous cell stage, tetrad stage, microspore stage, and pollen maturity stage. Compared with male fertile flower buds, in the microspore stage, the pollen sac wall tissue in the male sterile flower buds showed no signs of degeneration. In the pollen maturity stage, the tapetum and middle layer were not fully degraded, and anther development stopped. Therefore, the microspore stage was the key stage for anther abortion , and the pollen maturity stage was the post stage for anther abortion. A total of 4,108 differentially expressed genes were identified by transcriptome analysis. Among them, 1,899 were up-regulated, and 2,209 were down-regulated in the transcriptome of male sterile flower buds. We found that “protein kinase activity”, “apoptosis process”, “calcium binding”, “cell death”, “cytochrome c oxidase activity”, “aspartate peptidase activity”, “cysteine peptidase activity” and other biological pathways such as “starch and sucrose metabolism” and “proteasome” were closely related to male sterility in Prunus sibirica. A total of 331 key genes were preliminarily screened. CONCLUSION: The occurrence of male sterility in Prunus sibirica involved many biological processes and metabolic pathways. According to the results of microstructure observations, related physiological indexes determination and transcriptome analysis, we reveal that the occurrence of male sterility in Prunus sibirica may be caused by abnormal metabolic processes such as the release of cytochrome c in the male sterile flower buds, the imbalance of the antioxidant system being destroyed, and the inability of macromolecular substances such as starch to be converted into soluble small molecules at the correct stage of reproductive development, resulting in energy loss. As a result, the tapetum cannot be fully degraded, thereby blocking anther development, which eventually led to the formation of male sterility.
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spelling pubmed-85413192021-10-29 Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica Chen, Jianhua Xu, Hao Zhang, Jian Dong, Shengjun Liu, Quangang Wang, Ruoxi PeerJ Developmental Biology BACKGROUND: The phenomenon of male sterility widely occurs in Prunus sibirica and has a serious negative impact on yield. We identified the key stage and cause of male sterility and found differentially expressed genes related to male sterility in Prunus sibirica, and we analyzed the expression pattern of these genes. This work aimed to provide valuable reference and theoretical basis for the study of reproductive development and the mechanisms of male sterility in Prunus sibirica. METHOD: The microstructures of male sterile flower buds and male fertile flower buds were observed by paraffin section. Transcriptome sequencing was used to screen genes related to male sterility in Prunus sibirica. Quantitative real-time PCR analysis was performed to verify the transcriptome data. RESULTS: Anther development was divided into the sporogenous cell stage, tetrad stage, microspore stage, and pollen maturity stage. Compared with male fertile flower buds, in the microspore stage, the pollen sac wall tissue in the male sterile flower buds showed no signs of degeneration. In the pollen maturity stage, the tapetum and middle layer were not fully degraded, and anther development stopped. Therefore, the microspore stage was the key stage for anther abortion , and the pollen maturity stage was the post stage for anther abortion. A total of 4,108 differentially expressed genes were identified by transcriptome analysis. Among them, 1,899 were up-regulated, and 2,209 were down-regulated in the transcriptome of male sterile flower buds. We found that “protein kinase activity”, “apoptosis process”, “calcium binding”, “cell death”, “cytochrome c oxidase activity”, “aspartate peptidase activity”, “cysteine peptidase activity” and other biological pathways such as “starch and sucrose metabolism” and “proteasome” were closely related to male sterility in Prunus sibirica. A total of 331 key genes were preliminarily screened. CONCLUSION: The occurrence of male sterility in Prunus sibirica involved many biological processes and metabolic pathways. According to the results of microstructure observations, related physiological indexes determination and transcriptome analysis, we reveal that the occurrence of male sterility in Prunus sibirica may be caused by abnormal metabolic processes such as the release of cytochrome c in the male sterile flower buds, the imbalance of the antioxidant system being destroyed, and the inability of macromolecular substances such as starch to be converted into soluble small molecules at the correct stage of reproductive development, resulting in energy loss. As a result, the tapetum cannot be fully degraded, thereby blocking anther development, which eventually led to the formation of male sterility. PeerJ Inc. 2021-10-20 /pmc/articles/PMC8541319/ /pubmed/34722001 http://dx.doi.org/10.7717/peerj.12349 Text en ©2021 Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Developmental Biology
Chen, Jianhua
Xu, Hao
Zhang, Jian
Dong, Shengjun
Liu, Quangang
Wang, Ruoxi
Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title_full Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title_fullStr Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title_full_unstemmed Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title_short Transcriptomic analysis reveals candidate genes for male sterility in Prunus sibirica
title_sort transcriptomic analysis reveals candidate genes for male sterility in prunus sibirica
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541319/
https://www.ncbi.nlm.nih.gov/pubmed/34722001
http://dx.doi.org/10.7717/peerj.12349
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