Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation

Abstract ClpXP is the major protease in the mitochondrial matrix in eukaryotes, and is well conserved among species. ClpXP is composed of a proteolytic subunit, ClpP, and a chaperone-like subunit, ClpX. Although it has been proposed that ClpXP is required for the mitochondrial unfolded protein respo...

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Autores principales: Yuichi Matsushima, Yuta Hirofuji, Masamune Aihara, Song Yue, Takeshi Uchiumi, Laurie S. Kaguni, Dongchon Kang
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:847eacac284e4d42bb307b9085029b502021-12-02T11:53:01ZDrosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation10.1038/s41598-017-08088-62045-2322https://doaj.org/article/847eacac284e4d42bb307b9085029b502017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08088-6https://doaj.org/toc/2045-2322Abstract ClpXP is the major protease in the mitochondrial matrix in eukaryotes, and is well conserved among species. ClpXP is composed of a proteolytic subunit, ClpP, and a chaperone-like subunit, ClpX. Although it has been proposed that ClpXP is required for the mitochondrial unfolded protein response, additional roles for ClpXP in mitochondrial biogenesis are unclear. Here, we found that Drosophila leucine-rich pentatricopeptide repeat domain-containing protein 1 (DmLRPPRC1) is a specific substrate of ClpXP. Depletion or introduction of catalytically inactive mutation of ClpP increases DmLRPPRC1 and causes non-uniform increases of mitochondrial mRNAs, accumulation of some unprocessed mitochondrial transcripts, and modest repression of mitochondrial translation in Drosophila Schneider S2 cells. Moreover, DmLRPPRC1 over-expression induces the phenotypes similar to those observed when ClpP is depleted. Taken together, ClpXP regulates mitochondrial gene expression by changing the protein level of DmLRPPRC1 in Drosophila Schneider S2 cells.Yuichi MatsushimaYuta HirofujiMasamune AiharaSong YueTakeshi UchiumiLaurie S. KaguniDongchon KangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yuichi Matsushima
Yuta Hirofuji
Masamune Aihara
Song Yue
Takeshi Uchiumi
Laurie S. Kaguni
Dongchon Kang
Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
description Abstract ClpXP is the major protease in the mitochondrial matrix in eukaryotes, and is well conserved among species. ClpXP is composed of a proteolytic subunit, ClpP, and a chaperone-like subunit, ClpX. Although it has been proposed that ClpXP is required for the mitochondrial unfolded protein response, additional roles for ClpXP in mitochondrial biogenesis are unclear. Here, we found that Drosophila leucine-rich pentatricopeptide repeat domain-containing protein 1 (DmLRPPRC1) is a specific substrate of ClpXP. Depletion or introduction of catalytically inactive mutation of ClpP increases DmLRPPRC1 and causes non-uniform increases of mitochondrial mRNAs, accumulation of some unprocessed mitochondrial transcripts, and modest repression of mitochondrial translation in Drosophila Schneider S2 cells. Moreover, DmLRPPRC1 over-expression induces the phenotypes similar to those observed when ClpP is depleted. Taken together, ClpXP regulates mitochondrial gene expression by changing the protein level of DmLRPPRC1 in Drosophila Schneider S2 cells.
format article
author Yuichi Matsushima
Yuta Hirofuji
Masamune Aihara
Song Yue
Takeshi Uchiumi
Laurie S. Kaguni
Dongchon Kang
author_facet Yuichi Matsushima
Yuta Hirofuji
Masamune Aihara
Song Yue
Takeshi Uchiumi
Laurie S. Kaguni
Dongchon Kang
author_sort Yuichi Matsushima
title Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
title_short Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
title_full Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
title_fullStr Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
title_full_unstemmed Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation
title_sort drosophila protease clpxp specifically degrades dmlrpprc1 controlling mitochondrial mrna and translation
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/847eacac284e4d42bb307b9085029b50
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