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The pentatricopeptide repeat protein EMP603 is required for the splicing of mitochondrial Nad1 intron 2 and seed development in maize

Fan, Kaijian ; Ren, Zhenjing ; Zhang, Xiaofeng ; Liu, Yan ; Fu, Junjie ; Qi, Chunlai ; Tatar, Wurinile ; Rasmusson, Allan G. LU ; Wang, Guoying and Liu, Yunjun (2021) In Journal of Experimental Botany 72(20). p.6933-6948
Abstract

Intron splicing is an essential event in post-transcriptional RNA processing in plant mitochondria, which requires the participation of diverse nuclear-encoded splicing factors. However, it is presently unclear how these proteins cooperatively take part in the splicing of specific introns. In this study, we characterized a nuclear-encoded mitochondrial P-type pentatricopeptide repeat (PPR) protein named EMP603. This protein is essential for splicing of intron 2 in the Nad1 gene and interacts with the mitochondria-localized DEAD-box RNA helicase PMH2-5140, the RAD52-like proteins ODB1-0814 and ODB1-5061, and the CRM domain-containing protein Zm-mCSF1. Further study revealed that the N-terminal region of EMP603 interacts with the DEAD-box... (More)

Intron splicing is an essential event in post-transcriptional RNA processing in plant mitochondria, which requires the participation of diverse nuclear-encoded splicing factors. However, it is presently unclear how these proteins cooperatively take part in the splicing of specific introns. In this study, we characterized a nuclear-encoded mitochondrial P-type pentatricopeptide repeat (PPR) protein named EMP603. This protein is essential for splicing of intron 2 in the Nad1 gene and interacts with the mitochondria-localized DEAD-box RNA helicase PMH2-5140, the RAD52-like proteins ODB1-0814 and ODB1-5061, and the CRM domain-containing protein Zm-mCSF1. Further study revealed that the N-terminal region of EMP603 interacts with the DEAD-box of PMH2-5140, the CRM domain of Zm-mCSF1, and OBD1-5061, but not with OBD1-0814, whereas the PPR domain of EMP603 can interact with ODB1-0814, ODB1-5061, and PMH2-5140, but not with Zm-mCSF1. Defects in EMP603 severely disrupt the assembly and activity of mitochondrial complex I, leading to impaired mitochondrial function, and delayed seed development. The interactions revealed between EMP603 and PMH2-5140, ODB1-0814, ODB1-5061, and Zm-mCSF1 indicate a possible involvement of a dynamic 'spliceosome-like' complex in intron splicing, and may accelerate the elucidation of the intron splicing mechanism in plant mitochondria.

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author
; ; ; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Emp603, intron splicing, mitochondrion, PPR protein, seed development, Zea mays
in
Journal of Experimental Botany
volume
72
issue
20
pages
16 pages
publisher
Oxford University Press
external identifiers
  • pmid:34279607
  • scopus:85117181552
ISSN
0022-0957
DOI
10.1093/jxb/erab339
language
English
LU publication?
yes
id
0e344b7e-9334-4856-8d16-50f3d98d8329
date added to LUP
2022-02-08 12:48:37
date last changed
2024-04-18 06:24:51
@article{0e344b7e-9334-4856-8d16-50f3d98d8329,
  abstract     = {{<p>Intron splicing is an essential event in post-transcriptional RNA processing in plant mitochondria, which requires the participation of diverse nuclear-encoded splicing factors. However, it is presently unclear how these proteins cooperatively take part in the splicing of specific introns. In this study, we characterized a nuclear-encoded mitochondrial P-type pentatricopeptide repeat (PPR) protein named EMP603. This protein is essential for splicing of intron 2 in the Nad1 gene and interacts with the mitochondria-localized DEAD-box RNA helicase PMH2-5140, the RAD52-like proteins ODB1-0814 and ODB1-5061, and the CRM domain-containing protein Zm-mCSF1. Further study revealed that the N-terminal region of EMP603 interacts with the DEAD-box of PMH2-5140, the CRM domain of Zm-mCSF1, and OBD1-5061, but not with OBD1-0814, whereas the PPR domain of EMP603 can interact with ODB1-0814, ODB1-5061, and PMH2-5140, but not with Zm-mCSF1. Defects in EMP603 severely disrupt the assembly and activity of mitochondrial complex I, leading to impaired mitochondrial function, and delayed seed development. The interactions revealed between EMP603 and PMH2-5140, ODB1-0814, ODB1-5061, and Zm-mCSF1 indicate a possible involvement of a dynamic 'spliceosome-like' complex in intron splicing, and may accelerate the elucidation of the intron splicing mechanism in plant mitochondria. </p>}},
  author       = {{Fan, Kaijian and Ren, Zhenjing and Zhang, Xiaofeng and Liu, Yan and Fu, Junjie and Qi, Chunlai and Tatar, Wurinile and Rasmusson, Allan G. and Wang, Guoying and Liu, Yunjun}},
  issn         = {{0022-0957}},
  keywords     = {{Emp603; intron splicing; mitochondrion; PPR protein; seed development; Zea mays}},
  language     = {{eng}},
  month        = {{10}},
  number       = {{20}},
  pages        = {{6933--6948}},
  publisher    = {{Oxford University Press}},
  series       = {{Journal of Experimental Botany}},
  title        = {{The pentatricopeptide repeat protein EMP603 is required for the splicing of mitochondrial Nad1 intron 2 and seed development in maize}},
  url          = {{http://dx.doi.org/10.1093/jxb/erab339}},
  doi          = {{10.1093/jxb/erab339}},
  volume       = {{72}},
  year         = {{2021}},
}