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Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize
Pentatricopeptide repeat (PPR) proteins are one of the largest protein families, which consists of >400 members in most species. However, the molecular functions of many PPR proteins are still uncharacterized. Here, we isolated a maize mutant, defective kernel 40 (dek40). Positional cloning, and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859738/ https://www.ncbi.nlm.nih.gov/pubmed/31598687 http://dx.doi.org/10.1093/jxb/erz391 |
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author | Ren, Ru Chang Lu, Xiaoduo Zhao, Ya Jie Wei, Yi Ming Wang, Li Li Zhang, Lin Zhang, Wen Ting Zhang, Chunyi Zhang, Xian Sheng Zhao, Xiang Yu |
author_facet | Ren, Ru Chang Lu, Xiaoduo Zhao, Ya Jie Wei, Yi Ming Wang, Li Li Zhang, Lin Zhang, Wen Ting Zhang, Chunyi Zhang, Xian Sheng Zhao, Xiang Yu |
author_sort | Ren, Ru Chang |
collection | PubMed |
description | Pentatricopeptide repeat (PPR) proteins are one of the largest protein families, which consists of >400 members in most species. However, the molecular functions of many PPR proteins are still uncharacterized. Here, we isolated a maize mutant, defective kernel 40 (dek40). Positional cloning, and genetic and molecular analyses revealed that DEK40 encodes a new E+ subgroup PPR protein that is localized in the mitochondrion. DEK40 recognizes and directly binds to cox3, nad2, and nad5 transcripts and functions in their processing. In the dek40 mutant, abolishment of the C-to-U editing of cox3-314, nad2-26, and nad5-1916 leads to accumulated reactive oxygen species and promoted programmed cell death in endosperm cells due to the dysfunction of mitochondrial complexes I and IV. Furthermore, RNA sequencing analysis showed that gene expression in some pathways, such as glutathione metabolism and starch biosynthesis, was altered in the dek40 mutant compared with the wild-type control, which might be involved in abnormal development of the maize mutant kernels. Thus, our results provide solid evidence on the molecular mechanism underlying RNA editing by DEK40, and extend our understanding of PPR-E+ type protein in editing functions and kernel development in maize. |
format | Online Article Text |
id | pubmed-6859738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68597382019-11-21 Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize Ren, Ru Chang Lu, Xiaoduo Zhao, Ya Jie Wei, Yi Ming Wang, Li Li Zhang, Lin Zhang, Wen Ting Zhang, Chunyi Zhang, Xian Sheng Zhao, Xiang Yu J Exp Bot Research Papers Pentatricopeptide repeat (PPR) proteins are one of the largest protein families, which consists of >400 members in most species. However, the molecular functions of many PPR proteins are still uncharacterized. Here, we isolated a maize mutant, defective kernel 40 (dek40). Positional cloning, and genetic and molecular analyses revealed that DEK40 encodes a new E+ subgroup PPR protein that is localized in the mitochondrion. DEK40 recognizes and directly binds to cox3, nad2, and nad5 transcripts and functions in their processing. In the dek40 mutant, abolishment of the C-to-U editing of cox3-314, nad2-26, and nad5-1916 leads to accumulated reactive oxygen species and promoted programmed cell death in endosperm cells due to the dysfunction of mitochondrial complexes I and IV. Furthermore, RNA sequencing analysis showed that gene expression in some pathways, such as glutathione metabolism and starch biosynthesis, was altered in the dek40 mutant compared with the wild-type control, which might be involved in abnormal development of the maize mutant kernels. Thus, our results provide solid evidence on the molecular mechanism underlying RNA editing by DEK40, and extend our understanding of PPR-E+ type protein in editing functions and kernel development in maize. Oxford University Press 2019-11-01 2019-09-06 /pmc/articles/PMC6859738/ /pubmed/31598687 http://dx.doi.org/10.1093/jxb/erz391 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Papers Ren, Ru Chang Lu, Xiaoduo Zhao, Ya Jie Wei, Yi Ming Wang, Li Li Zhang, Lin Zhang, Wen Ting Zhang, Chunyi Zhang, Xian Sheng Zhao, Xiang Yu Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title | Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title_full | Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title_fullStr | Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title_full_unstemmed | Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title_short | Pentatricopeptide repeat protein DEK40 is required for mitochondrial function and kernel development in maize |
title_sort | pentatricopeptide repeat protein dek40 is required for mitochondrial function and kernel development in maize |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859738/ https://www.ncbi.nlm.nih.gov/pubmed/31598687 http://dx.doi.org/10.1093/jxb/erz391 |
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