Repository logo
 

Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila

Published version
Peer-reviewed

Change log

Authors

Andreazza, Simonetta 
Samstag, Colby 
Sanchez-Martinez, Alvaro 
Fernandez-Vizarra, Erika 

Abstract

Somatic mutations in the mitochondrial genome (mtDNA) have been linked to multiple disease conditions and to ageing itself. In Drosophila, knock-in of a proof-reading deficient mtDNA polymerase (POLG) generates high levels of somatic point mutations and also small indels, but surprisingly limited impact on organismal longevity or fitness. Here we describe a new mtDNA mutator model based on a mitochondrially-targeted cytidine deaminase, APOBEC1. mito-APOBEC1 acts as a potent mutagen which exclusively induces C:G>T:A transitions with no indels or mtDNA depletion. In these flies, the presence of multiple non-synonymous substitutions, even at modest heteroplasmy, disrupts mitochondrial function and dramatically impacts organismal fitness. A detailed analysis of the mutation profile in the POLG and mito-APOBEC1 models reveals that mutation type (quality) rather than quantity is a critical factor in impacting organismal fitness. The specificity for transition mutations and the severe phenotypes make mito-APOBEC1 an excellent mtDNA mutator model for ageing research.

Description

Keywords

APOBEC-1 Deaminase, Animals, DNA, Mitochondrial, Drosophila, Mitochondria, Models, Genetic, Mutation, Organisms, Genetically Modified

Journal Title

Nature Communications

Conference Name

Journal ISSN

2041-1723
2041-1723

Volume Title

10

Publisher

Nature Publishing Group
Sponsorship
European Research Council (309742)
Medical Research Council (MC_UP_1501/1)
Medical Research Council (MC_UU_00015/6)
Wellcome Trust (101876/Z/13/Z)
Wellcome Trust (212219/Z/18/Z)
Medical Research Council (MC_UU_00015/4)
Medical Research Council (MC_UU_00015/7)