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The S. pombe mitochondrial transcriptome

Mitochondrial gene expression is largely controlled through post-transcriptional processes including mitochondrial RNA (mt-RNA) processing, modification, decay, and quality control. Defective mitochondrial gene expression results in mitochondrial oxidative phosphorylation (OXPHOS) deficiency and has...

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Autores principales: Shang, Jinjie, Yang, Yanmei, Wu, Lin, Zou, Mengting, Huang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097661/
https://www.ncbi.nlm.nih.gov/pubmed/29954949
http://dx.doi.org/10.1261/rna.064477.117
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author Shang, Jinjie
Yang, Yanmei
Wu, Lin
Zou, Mengting
Huang, Ying
author_facet Shang, Jinjie
Yang, Yanmei
Wu, Lin
Zou, Mengting
Huang, Ying
author_sort Shang, Jinjie
collection PubMed
description Mitochondrial gene expression is largely controlled through post-transcriptional processes including mitochondrial RNA (mt-RNA) processing, modification, decay, and quality control. Defective mitochondrial gene expression results in mitochondrial oxidative phosphorylation (OXPHOS) deficiency and has been implicated in human disease. To fully understand mitochondrial transcription and RNA processing, we performed RNA-seq analyses of mt-RNAs from the fission yeast Schizosaccharomyces pombe. RNA-seq analyses show that the abundance of mt-RNAs vary greatly. Analysis of data also reveals mt-RNA processing sites including an unusual RNA cleavage event by mitochondrial tRNA (mt-tRNA) 5′-end processing enzyme RNase P. Additionally, this analysis reveals previously unknown mitochondrial transcripts including the rnpB-derived fragment, mitochondrial small RNAs (mitosRNAs) such as mt-tRNA-derived fragments (mt-tRFs) and mt-tRNA halves, and mt-tRNAs marked with 3′-CCACCA/CCACC in S. pombe. Finally, RNA-seq reveals that inactivation of trz2 encoding S. pombe mitochondrial tRNA 3′-end processing enzyme globally impairs mt-tRNA 3′-end processing, inhibits mt-mRNA 5′-end processing, and causes accumulation of unprocessed transcripts, demonstrating the feasibility of using RNA-seq to examine the protein known or predicted to be involved in mt-RNA processing in S. pombe. Our work uncovers the complexity of a fungal mitochondrial transcriptome and provides a framework for future studies of mitochondrial gene expression using S. pombe as a model system.
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spelling pubmed-60976612019-09-01 The S. pombe mitochondrial transcriptome Shang, Jinjie Yang, Yanmei Wu, Lin Zou, Mengting Huang, Ying RNA Article Mitochondrial gene expression is largely controlled through post-transcriptional processes including mitochondrial RNA (mt-RNA) processing, modification, decay, and quality control. Defective mitochondrial gene expression results in mitochondrial oxidative phosphorylation (OXPHOS) deficiency and has been implicated in human disease. To fully understand mitochondrial transcription and RNA processing, we performed RNA-seq analyses of mt-RNAs from the fission yeast Schizosaccharomyces pombe. RNA-seq analyses show that the abundance of mt-RNAs vary greatly. Analysis of data also reveals mt-RNA processing sites including an unusual RNA cleavage event by mitochondrial tRNA (mt-tRNA) 5′-end processing enzyme RNase P. Additionally, this analysis reveals previously unknown mitochondrial transcripts including the rnpB-derived fragment, mitochondrial small RNAs (mitosRNAs) such as mt-tRNA-derived fragments (mt-tRFs) and mt-tRNA halves, and mt-tRNAs marked with 3′-CCACCA/CCACC in S. pombe. Finally, RNA-seq reveals that inactivation of trz2 encoding S. pombe mitochondrial tRNA 3′-end processing enzyme globally impairs mt-tRNA 3′-end processing, inhibits mt-mRNA 5′-end processing, and causes accumulation of unprocessed transcripts, demonstrating the feasibility of using RNA-seq to examine the protein known or predicted to be involved in mt-RNA processing in S. pombe. Our work uncovers the complexity of a fungal mitochondrial transcriptome and provides a framework for future studies of mitochondrial gene expression using S. pombe as a model system. Cold Spring Harbor Laboratory Press 2018-09 /pmc/articles/PMC6097661/ /pubmed/29954949 http://dx.doi.org/10.1261/rna.064477.117 Text en © 2018 Shang et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Article
Shang, Jinjie
Yang, Yanmei
Wu, Lin
Zou, Mengting
Huang, Ying
The S. pombe mitochondrial transcriptome
title The S. pombe mitochondrial transcriptome
title_full The S. pombe mitochondrial transcriptome
title_fullStr The S. pombe mitochondrial transcriptome
title_full_unstemmed The S. pombe mitochondrial transcriptome
title_short The S. pombe mitochondrial transcriptome
title_sort s. pombe mitochondrial transcriptome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097661/
https://www.ncbi.nlm.nih.gov/pubmed/29954949
http://dx.doi.org/10.1261/rna.064477.117
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