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Neuroepigenetic signatures of age and sex in the living human brain

Authors :
Jacob M. Hooker
Matthew Louis Hibert
Umar Mahmood
Changning Wang
Joshua L. Roffman
Maria A Di Biase
Nicole R. Zürcher
Minhae Kim
Baileigh G. Hightower
Tonya M. Gilbert
Anisha Bhanot
Amanda E. Lyall
Douglas N. Greve
Ofer Pasternak
Marek Kubicki
Mary C. Catanese
Frederick A. Schroeder
Chieh-En Jane Tseng
Christine J. Wu
Hsiao-Ying Wey
Steven M. Stufflebeam
Anjali J. Parmar
Daphne J. Holt
Source :
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019), Nature Communications
Publication Year :
2019
Publisher :
Nature Portfolio, 2019.

Abstract

Age- and sex-related alterations in gene transcription have been demonstrated, however the underlying mechanisms are unresolved. Neuroepigenetic pathways regulate gene transcription in the brain. Here, we measure in vivo expression of the epigenetic enzymes, histone deacetylases (HDACs), across healthy human aging and between sexes using [11C]Martinostat positron emission tomography (PET) neuroimaging (n = 41). Relative HDAC expression increases with age in cerebral white matter, and correlates with age-associated disruptions in white matter microstructure. A post mortem study confirmed that HDAC1 and HDAC2 paralogs are elevated in white matter tissue from elderly donors. There are also sex-specific in vivo HDAC expression differences in brain regions associated with emotion and memory, including the amygdala and hippocampus. Hippocampus and white matter HDAC expression negatively correlates with emotion regulation skills (n = 23). Age and sex are associated with HDAC expression in vivo, which could drive age- and sex-related transcriptional changes and impact human behavior.<br />Gene transcription is known to vary with age and sex, although the underlying mechanisms are unresolved. Here, the authors show that epigenetic enzymes known as HDACs, which regulate gene transcription, are increasingly expressed with age in the living human brain, with sex differences also observed.

Details

Language :
English
ISSN :
20411723
Volume :
10
Issue :
1
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....66db91f6dcd6bbc9b339b5bacf19546d