Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
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
_version_ 1783471178908696576
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
work_keys_str_mv AT renruchang pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT luxiaoduo pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhaoyajie pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT weiyiming pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT wanglili pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhanglin pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhangwenting pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhangchunyi pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhangxiansheng pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize
AT zhaoxiangyu pentatricopeptiderepeatproteindek40isrequiredformitochondrialfunctionandkerneldevelopmentinmaize