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GWAS Study

Nuclear genome-wide associations with mitochondrial heteroplasmy.

Nandakumar P, Tian C, O'Connell J et al.

33731350 PubMed ID
GWAS Study Type
982072 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

NP
Nandakumar P
TC
Tian C
OJ
O'Connell J
HD
Hinds D
PA
Paterson AD
SN
Sondheimer N
Chapter II

Abstract

Summary of the research findings

The role of the nuclear genome in maintaining the stability of the mitochondrial genome (mtDNA) is incompletely known. mtDNA sequence variants can exist in a state of heteroplasmy, which denotes the coexistence of organellar genomes with different sequences. Heteroplasmic variants that impair mitochondrial capacity cause disease, and the state of heteroplasmy itself is deleterious. However, mitochondrial heteroplasmy may provide an intermediate state in the emergence of novel mitochondrial haplogroups. We used genome-wide genotyping data from 982,072 European ancestry individuals to evaluate variation in mitochondrial heteroplasmy and to identify the regions of the nuclear genome that affect it. Age, sex, and mitochondrial haplogroup were associated with the extent of heteroplasmy. GWAS identified 20 loci for heteroplasmy that exceeded genome-wide significance. This included a region overlapping mitochondrial transcription factor A (TFAM), which has multiple roles in mtDNA packaging, replication, and transcription. These results show that mitochondrial heteroplasmy has a heritable nuclear component.

982,072 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

982072
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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