Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.

Faithful inheritance of mitochondrial DNA (mtDNA) is crucial for cellular respiration/oxidative phosphorylation and mitochondrial membrane potential. However, how mtDNA is transmitted to progeny is not fully understood. We utilized hypersuppressive mtDNA, a class of respiratory deficient Saccharomyc...

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Autores principales: Daniel Corbi, Angelika Amon
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/f909f2d7178f451eac63b3dc87e1101b
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spelling oai:doaj.org-article:f909f2d7178f451eac63b3dc87e1101b2021-12-02T20:03:31ZDecreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.1553-73901553-740410.1371/journal.pgen.1009808https://doaj.org/article/f909f2d7178f451eac63b3dc87e1101b2021-10-01T00:00:00Zhttps://doi.org/10.1371/journal.pgen.1009808https://doaj.org/toc/1553-7390https://doaj.org/toc/1553-7404Faithful inheritance of mitochondrial DNA (mtDNA) is crucial for cellular respiration/oxidative phosphorylation and mitochondrial membrane potential. However, how mtDNA is transmitted to progeny is not fully understood. We utilized hypersuppressive mtDNA, a class of respiratory deficient Saccharomyces cerevisiae mtDNA that is preferentially inherited over wild-type mtDNA (rho+), to uncover the factors governing mtDNA inheritance. We found that some regions of rho+ mtDNA persisted while others were lost after a specific hypersuppressive takeover indicating that hypersuppressive preferential inheritance may partially be due to active destruction of rho+ mtDNA. From a multicopy suppression screen, we found that overexpression of putative mitochondrial RNA exonuclease PET127 reduced biased inheritance of a subset of hypersuppressive genomes. This suppression required PET127 binding to the mitochondrial RNA polymerase RPO41 but not PET127 exonuclease activity. A temperature-sensitive allele of RPO41 improved rho+ mtDNA inheritance over a specific hypersuppressive mtDNA at semi-permissive temperatures revealing a previously unknown role for rho+ transcription in promoting hypersuppressive mtDNA inheritance.Daniel CorbiAngelika AmonPublic Library of Science (PLoS)articleGeneticsQH426-470ENPLoS Genetics, Vol 17, Iss 10, p e1009808 (2021)
institution DOAJ
collection DOAJ
language EN
topic Genetics
QH426-470
spellingShingle Genetics
QH426-470
Daniel Corbi
Angelika Amon
Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
description Faithful inheritance of mitochondrial DNA (mtDNA) is crucial for cellular respiration/oxidative phosphorylation and mitochondrial membrane potential. However, how mtDNA is transmitted to progeny is not fully understood. We utilized hypersuppressive mtDNA, a class of respiratory deficient Saccharomyces cerevisiae mtDNA that is preferentially inherited over wild-type mtDNA (rho+), to uncover the factors governing mtDNA inheritance. We found that some regions of rho+ mtDNA persisted while others were lost after a specific hypersuppressive takeover indicating that hypersuppressive preferential inheritance may partially be due to active destruction of rho+ mtDNA. From a multicopy suppression screen, we found that overexpression of putative mitochondrial RNA exonuclease PET127 reduced biased inheritance of a subset of hypersuppressive genomes. This suppression required PET127 binding to the mitochondrial RNA polymerase RPO41 but not PET127 exonuclease activity. A temperature-sensitive allele of RPO41 improved rho+ mtDNA inheritance over a specific hypersuppressive mtDNA at semi-permissive temperatures revealing a previously unknown role for rho+ transcription in promoting hypersuppressive mtDNA inheritance.
format article
author Daniel Corbi
Angelika Amon
author_facet Daniel Corbi
Angelika Amon
author_sort Daniel Corbi
title Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
title_short Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
title_full Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
title_fullStr Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
title_full_unstemmed Decreasing mitochondrial RNA polymerase activity reverses biased inheritance of hypersuppressive mtDNA.
title_sort decreasing mitochondrial rna polymerase activity reverses biased inheritance of hypersuppressive mtdna.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/f909f2d7178f451eac63b3dc87e1101b
work_keys_str_mv AT danielcorbi decreasingmitochondrialrnapolymeraseactivityreversesbiasedinheritanceofhypersuppressivemtdna
AT angelikaamon decreasingmitochondrialrnapolymeraseactivityreversesbiasedinheritanceofhypersuppressivemtdna
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