A TOMM40 poly-T variant modulates gene expression and is associated with vocabulary ability and decline in nonpathologic aging

Payton, A, Sindrewicz, P, Pessoa, V, Platt, H, Horan, M, Ollier, W, Bubb, VJ ORCID: 0000-0003-2763-7004, Pendleton, N and Quinn, JP ORCID: 0000-0003-3551-7803 (2016) A TOMM40 poly-T variant modulates gene expression and is associated with vocabulary ability and decline in nonpathologic aging. Neurobiology of Aging, 39. 217.e1-217.e7.

Text accepted version.pdf - Unspecified Available under License Creative Commons Attribution Non-commercial No Derivatives. Download (359kB)

Abstract

The Translocase of Outer Mitochondrial Membrane 40 Homolog and Apolipoprotein E (TOMM40-APOE) locus has been associated with a number of age-related phenotypes in humans including nonpathologic cognitive aging, late-onset Alzheimer's disease, and longevity. Here, we investigate the influence of the TOMM40 intron 6 poly-T variant (rs10524523) on TOMM40 gene expression and cognitive abilities and decline in a cohort of 1613 community-dwelling elderly volunteers who had been followed for changes in cognitive functioning over a period of 14 years (range = 12–18 years). We showed that the shorter length poly-T variants were found to act as a repressor of luciferase gene expression in reporter gene constructs. Expression was reduced to approximately half of that observed for the very long variant. We further observed that the shorter poly-T variant was significantly associated with reduced vocabulary ability and a slower rate of vocabulary decline with age compared to the very long poly-T variants. No significant associations were observed for memory, fluid intelligence or processing speed, although the direction of effect, where the short variant was correlated with reduced ability and slower rate of decline was observed for all tests. Our results indicate that the poly-T variant has the ability to interact with transcription machinery and differentially modulate reporter gene expression and influence vocabulary ability and decline with age.

Item Type:	Article
Uncontrolled Keywords:	TOMM40, Cognition, Aging, Retrotransposon, APOE, Expression
Subjects:	?? RC ?? ?? RC0321 ??
Depositing User:	Symplectic Admin
Date Deposited:	03 Feb 2016 09:55
Last Modified:	15 Dec 2022 11:28
DOI:	10.1016/j.neurobiolaging.2015.11.017
Related URLs:	Author Publisher
URI:	https://livrepository.liverpool.ac.uk/id/eprint/2048319