Regional differences in gene expression and promoter usage in aged human brains

Luba M. Pardo, Patrizia Rizzu, Margherita Francescatto, Morana Vitezic, Gwenaël G.R. Leday, Javier Simon Sanchez, Abdullah Khamis, Hazuki Takahashi, Wilma D.J. van de Berg, Yulia A. Medvedeva, Mark A. van de Wiel, Carsten O. Daub, Piero Carninci, Peter Heutink*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

28 Citations (Scopus)

Abstract

To characterize the promoterome of caudate and putamen regions (striatum), frontal and temporal cortices, and hippocampi from aged human brains, we used high-throughput cap analysis of gene expression to profile the transcription start sites and to quantify the differences in gene expression across the 5 brain regions. We also analyzed the extent to which methylation influenced the observed expression profiles. We sequenced more than 71 million cap analysis of gene expression tags corresponding to 70,202 promoter regions and 16,888 genes. More than 7000 transcripts were differentially expressed, mainly because of differential alternative promoter usage. Unexpectedly, 7% of differentially expressed genes were neurodevelopmental transcription factors. Functional pathway analysis on the differentially expressed genes revealed an overrepresentation of several signaling pathways (e.g., fibroblast growth factor and wnt signaling) in hippocampus and striatum. We also found that although 73% of methylation signals mapped within genes, the influence of methylation on the expression profile was small. Our study underscores alternative promoter usage as an important mechanism for determining the regional differences in gene expression at old age.

Original languageEnglish
Pages (from-to)1825-1836
Number of pages12
JournalNeurobiology of Aging
Volume34
Issue number7
DOIs
Publication statusPublished - Jul 2013
Externally publishedYes

Bibliographical note

Copyright: 2013 Elsevier Inc.

Fingerprint

Dive into the research topics of 'Regional differences in gene expression and promoter usage in aged human brains'. Together they form a unique fingerprint.

Cite this