The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseases-Reference-Cited by-同舟云学术

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The disease-causing mutation p.F907I reveals a novel pathogenic mechanism for POLγ-related diseases

Published:2023-10 Issue:7 Volume:1869 Page:166786
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Erdinc Direnis,Macao Bertil,Valenzuela Sebastian,Lesko Nicole,Naess Karin,Peter Bradley,Bruhn Helene,Wedell Anna,Wredenberg Anna,Falkenberg Maria

Funder

Novo Nordisk Fonden

Västra Götalandsregionen

Swedish Cancer Foundation

IngaBritt och Arne Lundbergs Forskningsstiftelse

Knut och Alice Wallenbergs Stiftelse

Vetenskapsrådet

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference32 articles.

1. DNA replication and transcription in mammalian mitochondria;Falkenberg;Annu. Rev. Biochem.,2007

2. The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance;Lim;J. Biol. Chem.,1999

3. Replication of mitochondrial DNA occurs by strand displacement with alternative light-strand origins, not via a strand-coupled mechanism;Brown;Genes Dev.,2005

4. Mitochondrial RNA polymerase is needed for activation of the origin of light-strand DNA replication;Fuste;Mol. Cell,2010

5. In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replication;Wanrooij;EMBO Rep.,2012

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