Heteroplasmy concordance between mitochondrial DNA and RNA.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 09 2019
Historique:
received: 24 05 2019
accepted: 12 08 2019
entrez: 12 9 2019
pubmed: 12 9 2019
medline: 31 10 2020
Statut: epublish

Résumé

Mitochondrial DNA (mtDNA) heteroplasmies are associated with various diseases but the transmission of heteroplasmy from mtDNA to mitochondrial RNA (mtRNA) remains unclear. We compared heteroplasmies in mtRNA from 446 human B-lymphoblastoid cell lines to their corresponding mtDNA using deep sequencing data from two independent studies. We observed 2786 heteroplasmies presenting in both DNA and RNA at 1% frequency cutoff. Among them, the frequencies of 2427 (87.1%) heteroplasmies were highly consistent (less than 5% frequency difference) between DNA and RNA. To validate these frequency consistencies, we isolated DNA and RNA simultaneously from GM12282 cell line used in those two sequencing studies, and resequenced its heteroplasmy sites. Interestingly, we also observed the rapid changes of heteroplasmy frequencies during 4 weeks of the cell culture: the frequencies at Day 14 increased by >25% than those at Day 0. However, the heteroplasmy frequencies from the same time point were highly consistent. In summary, our analysis on public data together with in vitro study indicates that the heteroplasmies in DNA can be transcribed into RNA with high fidelity. Meanwhile, the observed rapid-changing heteroplasmy frequency can potentially disturb cell functions, which could be an overlooked confounding factor in cell line related studies.

Identifiants

pubmed: 31506522
doi: 10.1038/s41598-019-49279-7
pii: 10.1038/s41598-019-49279-7
pmc: PMC6737107
doi:

Substances chimiques

DNA, Mitochondrial 0
RNA, Mitochondrial 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

12942

Subventions

Organisme : NHLBI NIH HHS
ID : P01 HL108801
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL112747
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI085286
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002384
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002385
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL079904
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL114501
Pays : United States

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Auteurs

Ruoyu Zhang (R)

Division of Nutritional Sciences, Cornell University, Ithaca, New York, 14853, USA. rz253@cornell.deu.
Regeneron Pharmaceuticals, Inc, Tarrytown, NY, 10591, USA. rz253@cornell.deu.

Kiichi Nakahira (K)

Division of Pulmonary and Critical Care Medicine, Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medicine, New York, NY, 10065, USA.
Department of Pharmacology, Nara Medical University, Kashihara-shi, Nara, Japan.

Augustine M K Choi (AMK)

Division of Pulmonary and Critical Care Medicine, Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medicine, New York, NY, 10065, USA.

Zhenglong Gu (Z)

Division of Nutritional Sciences, Cornell University, Ithaca, New York, 14853, USA. zg27@cornell.edu.

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Classifications MeSH