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The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity

To generate energy efficiently, the cell is uniquely challenged to co-ordinate the abundance of electron transport chain protein subunits expressed from both nuclear and mitochondrial genomes. How an effective stoichiometry of this many constituent subunits is co-ordinated post-transcriptionally rem...

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Autores principales: Sirey, Tamara M, Roberts, Kenny, Haerty, Wilfried, Bedoya-Reina, Oscar, Rogatti-Granados, Sebastian, Tan, Jennifer Y, Li, Nick, Heather, Lisa C, Carter, Roderick N, Cooper, Sarah, Finch, Andrew J, Wills, Jimi, Morton, Nicholas M, Marques, Ana Claudia, Ponting, Chris P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542586/
https://www.ncbi.nlm.nih.gov/pubmed/31045494
http://dx.doi.org/10.7554/eLife.45051
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author Sirey, Tamara M
Roberts, Kenny
Haerty, Wilfried
Bedoya-Reina, Oscar
Rogatti-Granados, Sebastian
Tan, Jennifer Y
Li, Nick
Heather, Lisa C
Carter, Roderick N
Cooper, Sarah
Finch, Andrew J
Wills, Jimi
Morton, Nicholas M
Marques, Ana Claudia
Ponting, Chris P
author_facet Sirey, Tamara M
Roberts, Kenny
Haerty, Wilfried
Bedoya-Reina, Oscar
Rogatti-Granados, Sebastian
Tan, Jennifer Y
Li, Nick
Heather, Lisa C
Carter, Roderick N
Cooper, Sarah
Finch, Andrew J
Wills, Jimi
Morton, Nicholas M
Marques, Ana Claudia
Ponting, Chris P
author_sort Sirey, Tamara M
collection PubMed
description To generate energy efficiently, the cell is uniquely challenged to co-ordinate the abundance of electron transport chain protein subunits expressed from both nuclear and mitochondrial genomes. How an effective stoichiometry of this many constituent subunits is co-ordinated post-transcriptionally remains poorly understood. Here we show that Cerox1, an unusually abundant cytoplasmic long noncoding RNA (lncRNA), modulates the levels of mitochondrial complex I subunit transcripts in a manner that requires binding to microRNA-488-3p. Increased abundance of Cerox1 cooperatively elevates complex I subunit protein abundance and enzymatic activity, decreases reactive oxygen species production, and protects against the complex I inhibitor rotenone. Cerox1 function is conserved across placental mammals: human and mouse orthologues effectively modulate complex I enzymatic activity in mouse and human cells, respectively. Cerox1 is the first lncRNA demonstrated, to our knowledge, to regulate mitochondrial oxidative phosphorylation and, with miR-488-3p, represent novel targets for the modulation of complex I activity.
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spelling pubmed-65425862019-06-12 The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity Sirey, Tamara M Roberts, Kenny Haerty, Wilfried Bedoya-Reina, Oscar Rogatti-Granados, Sebastian Tan, Jennifer Y Li, Nick Heather, Lisa C Carter, Roderick N Cooper, Sarah Finch, Andrew J Wills, Jimi Morton, Nicholas M Marques, Ana Claudia Ponting, Chris P eLife Biochemistry and Chemical Biology To generate energy efficiently, the cell is uniquely challenged to co-ordinate the abundance of electron transport chain protein subunits expressed from both nuclear and mitochondrial genomes. How an effective stoichiometry of this many constituent subunits is co-ordinated post-transcriptionally remains poorly understood. Here we show that Cerox1, an unusually abundant cytoplasmic long noncoding RNA (lncRNA), modulates the levels of mitochondrial complex I subunit transcripts in a manner that requires binding to microRNA-488-3p. Increased abundance of Cerox1 cooperatively elevates complex I subunit protein abundance and enzymatic activity, decreases reactive oxygen species production, and protects against the complex I inhibitor rotenone. Cerox1 function is conserved across placental mammals: human and mouse orthologues effectively modulate complex I enzymatic activity in mouse and human cells, respectively. Cerox1 is the first lncRNA demonstrated, to our knowledge, to regulate mitochondrial oxidative phosphorylation and, with miR-488-3p, represent novel targets for the modulation of complex I activity. eLife Sciences Publications, Ltd 2019-05-02 /pmc/articles/PMC6542586/ /pubmed/31045494 http://dx.doi.org/10.7554/eLife.45051 Text en © 2019, Sirey et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Sirey, Tamara M
Roberts, Kenny
Haerty, Wilfried
Bedoya-Reina, Oscar
Rogatti-Granados, Sebastian
Tan, Jennifer Y
Li, Nick
Heather, Lisa C
Carter, Roderick N
Cooper, Sarah
Finch, Andrew J
Wills, Jimi
Morton, Nicholas M
Marques, Ana Claudia
Ponting, Chris P
The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title_full The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title_fullStr The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title_full_unstemmed The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title_short The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity
title_sort long non-coding rna cerox1 is a post transcriptional regulator of mitochondrial complex i catalytic activity
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542586/
https://www.ncbi.nlm.nih.gov/pubmed/31045494
http://dx.doi.org/10.7554/eLife.45051
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