Ontology highlight
ABSTRACT:
SUBMITTER: Friedlander SM
PROVIDER: S-EPMC3554748 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
Friedlander Scott M SM Herrmann Amanda L AL Lowry Daniel P DP Mepham Emily R ER Lek Monkol M North Kathryn N KN Organ Chris L CL
PloS one 20130124 1
A premature stop codon in ACTN3 resulting in α-actinin-3 deficiency (the ACTN3 577XX genotype) is common in humans and reduces strength, muscle mass, and fast-twitch fiber diameter, but increases the metabolic efficiency of skeletal muscle. Linkage disequilibrium data suggest that the ACTN3 R577X allele has undergone positive selection during human evolution. The allele has been hypothesized to be adaptive in environments with scarce resources where efficient muscle metabolism would be selected. ...[more]