TY - JOUR
T1 - Regional differences in gene expression and promoter usage in aged human brains
AU - Pardo, Luba M.
AU - Rizzu, Patrizia
AU - Francescatto, Margherita
AU - Vitezic, Morana
AU - Leday, Gwenaël G.R.
AU - Sanchez, Javier Simon
AU - Khamis, Abdullah M.
AU - Takahashi, Hazuki
AU - van de Berg, Wilma D.J.
AU - Medvedeva, Yulia
AU - van de Wiel, Mark A.
AU - Daub, Carsten O.
AU - Carninci, Piero
AU - Heutink, Peter
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2013/2/19
Y1 - 2013/2/19
N2 - 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.
AB - 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.
UR - http://hdl.handle.net/10754/552356
UR - http://linkinghub.elsevier.com/retrieve/pii/S0197458013000237
UR - http://www.scopus.com/inward/record.url?scp=84875851114&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2013.01.005
DO - 10.1016/j.neurobiolaging.2013.01.005
M3 - Article
SN - 0197-4580
VL - 34
SP - 1825
EP - 1836
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 7
ER -