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J Gerontol A Biol Sci Med Sci. 2012 Nov;67(11):1132-9. doi: 10.1093/gerona/gls067. Epub 2012 Mar 28.

FOXO3 gene variants and human aging: coding variants may not be key players.

Author information

1
Honolulu Heart Program, Kuakini Medical Center, Honolulu Hawaii, USA. donlon@hawaii.edu

Abstract

FOXO3 is generally recognized as a "master" gene in aging since its association with longevity has been replicated in multiple organisms and human populations. A group of single nucleotide polymorphisms in linkage disequilibrium with a coding region has been associated with human longevity, but the actual functional variant is unidentified. Therefore, we sequenced the coding region in our long-lived Japanese American population in order to enhance resources for fine mapping this region. We demonstrate that of 38 published variants, 6 are misalignments with homologous nonallelic sequences from FOXO3B (ZNF286B), a pseudogene on a different chromosome; 2 are attributable to ZNF286B only, and the remaining 30 were unconfirmed, indicating that they are very rare and not likely involved in longevity. Furthermore, we identified a novel, unique, nonsynonymous coding variant in exon 3 (Gly566Ala; rs138174682) that is prevalent in multiple ethnic groups but appeared too rare for major longevity effects in our study populations.

PMID:
22459618
PMCID:
PMC3668389
DOI:
10.1093/gerona/gls067
[Indexed for MEDLINE]
Free PMC Article

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