Functional Genomic Analysis of Human Mitochondrial RNA Processing

Both strands of human mtDNA are transcribed in continuous, multigenic units that are cleaved into the mature rRNAs, tRNAs, and mRNAs required for respiratory chain biogenesis. We sought to systematically identify nuclear-encoded proteins that contribute to processing of mtRNAs within the organelle....

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Main Authors: Ashley R. Wolf, Vamsi K. Mootha
Format: Article
Language:English
Published: Elsevier 2014-05-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124714002137
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author Ashley R. Wolf
Vamsi K. Mootha
author_facet Ashley R. Wolf
Vamsi K. Mootha
author_sort Ashley R. Wolf
collection DOAJ
description Both strands of human mtDNA are transcribed in continuous, multigenic units that are cleaved into the mature rRNAs, tRNAs, and mRNAs required for respiratory chain biogenesis. We sought to systematically identify nuclear-encoded proteins that contribute to processing of mtRNAs within the organelle. First, we devised and validated a multiplex MitoString assay that quantitates 27 mature and precursor mtDNA transcripts. Second, we applied MitoString profiling to evaluate the impact of silencing each of 107 mitochondrial-localized, predicted RNA-binding proteins. With the resulting data set, we rediscovered the roles of recently identified RNA-processing enzymes, detected unanticipated roles of known disease genes in RNA processing, and identified new regulatory factors. We demonstrate that one such factor, FASTKD4, modulates the half-lives of a subset of mt-mRNAs and associates with mtRNAs in vivo. MitoString profiling may be useful for diagnosing and deciphering the pathogenesis of mtDNA disorders.
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spelling doaj.art-18bd68fafe664948bd53b2bb7d482aa32022-12-21T19:41:36ZengElsevierCell Reports2211-12472014-05-017391893110.1016/j.celrep.2014.03.035Functional Genomic Analysis of Human Mitochondrial RNA ProcessingAshley R. Wolf0Vamsi K. Mootha1Howard Hughes Medical Institute, Department of Molecular Biology, and Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USAHoward Hughes Medical Institute, Department of Molecular Biology, and Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USABoth strands of human mtDNA are transcribed in continuous, multigenic units that are cleaved into the mature rRNAs, tRNAs, and mRNAs required for respiratory chain biogenesis. We sought to systematically identify nuclear-encoded proteins that contribute to processing of mtRNAs within the organelle. First, we devised and validated a multiplex MitoString assay that quantitates 27 mature and precursor mtDNA transcripts. Second, we applied MitoString profiling to evaluate the impact of silencing each of 107 mitochondrial-localized, predicted RNA-binding proteins. With the resulting data set, we rediscovered the roles of recently identified RNA-processing enzymes, detected unanticipated roles of known disease genes in RNA processing, and identified new regulatory factors. We demonstrate that one such factor, FASTKD4, modulates the half-lives of a subset of mt-mRNAs and associates with mtRNAs in vivo. MitoString profiling may be useful for diagnosing and deciphering the pathogenesis of mtDNA disorders.http://www.sciencedirect.com/science/article/pii/S2211124714002137
spellingShingle Ashley R. Wolf
Vamsi K. Mootha
Functional Genomic Analysis of Human Mitochondrial RNA Processing
Cell Reports
title Functional Genomic Analysis of Human Mitochondrial RNA Processing
title_full Functional Genomic Analysis of Human Mitochondrial RNA Processing
title_fullStr Functional Genomic Analysis of Human Mitochondrial RNA Processing
title_full_unstemmed Functional Genomic Analysis of Human Mitochondrial RNA Processing
title_short Functional Genomic Analysis of Human Mitochondrial RNA Processing
title_sort functional genomic analysis of human mitochondrial rna processing
url http://www.sciencedirect.com/science/article/pii/S2211124714002137
work_keys_str_mv AT ashleyrwolf functionalgenomicanalysisofhumanmitochondrialrnaprocessing
AT vamsikmootha functionalgenomicanalysisofhumanmitochondrialrnaprocessing