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Titel:

Genes Whose Gain or Loss-of-Function Increases Endurance Performance in Mice: A Systematic Literature Review

Dokumenttyp:
Zeitschriftenaufsatz
Autor(en):
Yaghoob Nezhad F, Verbrugge SAJ, Schoenfelder M, Becker L, Hrabeˇ de Angelis M, Wackerhage H
Abstract:
Endurance is not only a key factor in many sports but endurance-related variables are also associated with good health and low mortality. Twin and family studies suggest that several endurance-associated traits are ≈50% inherited. However, we still poorly understand what DNA sequence variants contribute to endurance heritability. To address this issue, we conducted a systematic review to identify genes whose experimental loss or gain-of-function increases endurance capacity in mice. We found 31 genes including two isoforms of Ppargc1a whose manipulation increases running or swimming endurance performance by up to 1800%. Genes whose gain-of-function increases endurance are Adcy5, Adcy8, Hk2, Il15, Mef2c, Nr4a3, Pck1 (Pepck), Ppard, Ppargc1a (both the a and b isoforms of the protein Pgc-1α), Ppargc1b, Ppp3ca (calcineurin), Scd1, Slc5a7, Tfe3, Tfeb, Trib3 & Trpv1. Genes whose loss-of-function increases endurance in mice are Actn3, Adrb2, Bdkrb2, Cd47, Crym, Hif1a, Myoz1, Pappa, Pknox1, Pten, Sirt4, Thbs1, Thra, and Tnfsf12. Of these genes, human DNA sequence variants of ACTN3, ADCY5, ADRB2, BDKRB2, HIF1A, PPARD, PPARGC1A, PPARGC1B, and PPP3CA are also associated with endurance capacity and/or VO2max trainability suggesting evolutionary conservation between mice and humans. Bioinformatical analyses show that there are numerous amino acid or copy number-changing DNA variants of endurance genes in humans, suggesting that genetic variation of endurance genes contributes to the variation of human endurance capacity, too. Moreover, several of these genes/proteins change their expression or phosphorylation in skeletal muscle or the heart after endurance exercise, suggesting a role in the adaptation to endurance exercise.
Stichworte:
endurance, running, transgenic mice, genetics, mitochondrial biogenesis, GWAS, oxygen uptake, metabolism
Dewey Dezimalklassifikation:
570 Biowissenschaften, Biologie; 610 Medizin und Gesundheit; 790 Sport, Spiele, Unterhaltung
Zeitschriftentitel:
Frontiers in Physiology
Jahr:
2019
Band / Volume:
10
Jahr / Monat:
2019-03
Quartal:
1. Quartal
Monat:
Mar
Seitenangaben Beitrag:
14
Reviewed:
ja
Sprache:
en
Volltext / DOI:
doi:10.3389/fphys.2019.00262
WWW:
https://www.frontiersin.org/articles/10.3389/fphys.2019.00262/full
E-ISSN:
1664-042X
Impact Factor:
3.394
Publikationsdatum:
22.03.2019
Semester:
WS 18-19
TUM Einrichtung:
Sportbiologie
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