Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain

Glucocorticoids and the glucocorticoid (GR) and mineralocorticoid (MR) receptors have been implicated in many processes, particularly in negative feedback regulation of the hypothalamic-pituitary-adrenal axis. Epigenetically programmed GR alternative promoter usage underlies transcriptional control...

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Main Authors: Cao-Lei L., Suwansirikul S., Jutavijittum P., Meriaux S.B., Turner J.D., Muller C.P.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84884416988&partnerID=40&md5=4f30d20df1e10c04190f4a86a6873f16
http://www.ncbi.nlm.nih.gov/pubmed/23948638
http://cmuir.cmu.ac.th/handle/6653943832/4145
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-41452014-08-30T02:35:43Z Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain Cao-Lei L. Suwansirikul S. Jutavijittum P. Meriaux S.B. Turner J.D. Muller C.P. Glucocorticoids and the glucocorticoid (GR) and mineralocorticoid (MR) receptors have been implicated in many processes, particularly in negative feedback regulation of the hypothalamic-pituitary-adrenal axis. Epigenetically programmed GR alternative promoter usage underlies transcriptional control of GR levels, generation of GR 3' splice variants, and the overall GC response in the brain. No detailed analysis of GR first exons or GR transcript variants throughout the human brain has been reported. Therefore we investigated post mortem tissues from 28 brain regions of 5 individuals. GR first exons were expressed throughout the healthy human brain with no region-specific usage patterns. First exon levels were highly inter-correlated suggesting that they are co-regulated. GR 3' splice variants (GRα and GR-P) were equally distributed in all regions, and GRβ expression was always low. GR/MR ratios showed significant differences between the 28 tissues with the highest ratio in the pituitary gland. Modification levels of individual CpG dinucleotides, including 5-mC and 5-hmC, in promoters 1D, 1E, 1F, and 1H were low, and diffusely clustered; despite significant heterogeneity between the donors. In agreement with this clustering, sum modification levels rather than individual CpG modifications correlated with GR expression. Two-way ANOVA showed that this sum modification was both promoter and brain region specific, but that there was however no promoter*tissue interaction. The heterogeneity between donors may however hide such an interaction. In both promoters 1F and 1H modification levels correlated with GRα expression suggesting that 5-mC and 5-hmC play an important role in fine tuning GR expression levels throughout the brain. © 2013 Elsevier Ltd. 2014-08-30T02:35:43Z 2014-08-30T02:35:43Z 2013 Article 00223956 10.1016/j.jpsychires.2013.07.022 JPYRA http://www.scopus.com/inward/record.url?eid=2-s2.0-84884416988&partnerID=40&md5=4f30d20df1e10c04190f4a86a6873f16 http://www.ncbi.nlm.nih.gov/pubmed/23948638 http://cmuir.cmu.ac.th/handle/6653943832/4145 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Glucocorticoids and the glucocorticoid (GR) and mineralocorticoid (MR) receptors have been implicated in many processes, particularly in negative feedback regulation of the hypothalamic-pituitary-adrenal axis. Epigenetically programmed GR alternative promoter usage underlies transcriptional control of GR levels, generation of GR 3' splice variants, and the overall GC response in the brain. No detailed analysis of GR first exons or GR transcript variants throughout the human brain has been reported. Therefore we investigated post mortem tissues from 28 brain regions of 5 individuals. GR first exons were expressed throughout the healthy human brain with no region-specific usage patterns. First exon levels were highly inter-correlated suggesting that they are co-regulated. GR 3' splice variants (GRα and GR-P) were equally distributed in all regions, and GRβ expression was always low. GR/MR ratios showed significant differences between the 28 tissues with the highest ratio in the pituitary gland. Modification levels of individual CpG dinucleotides, including 5-mC and 5-hmC, in promoters 1D, 1E, 1F, and 1H were low, and diffusely clustered; despite significant heterogeneity between the donors. In agreement with this clustering, sum modification levels rather than individual CpG modifications correlated with GR expression. Two-way ANOVA showed that this sum modification was both promoter and brain region specific, but that there was however no promoter*tissue interaction. The heterogeneity between donors may however hide such an interaction. In both promoters 1F and 1H modification levels correlated with GRα expression suggesting that 5-mC and 5-hmC play an important role in fine tuning GR expression levels throughout the brain. © 2013 Elsevier Ltd.
format Article
author Cao-Lei L.
Suwansirikul S.
Jutavijittum P.
Meriaux S.B.
Turner J.D.
Muller C.P.
spellingShingle Cao-Lei L.
Suwansirikul S.
Jutavijittum P.
Meriaux S.B.
Turner J.D.
Muller C.P.
Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
author_facet Cao-Lei L.
Suwansirikul S.
Jutavijittum P.
Meriaux S.B.
Turner J.D.
Muller C.P.
author_sort Cao-Lei L.
title Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
title_short Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
title_full Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
title_fullStr Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
title_full_unstemmed Glucocorticoid receptor gene expression and promoter CpG modifications throughout the human brain
title_sort glucocorticoid receptor gene expression and promoter cpg modifications throughout the human brain
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84884416988&partnerID=40&md5=4f30d20df1e10c04190f4a86a6873f16
http://www.ncbi.nlm.nih.gov/pubmed/23948638
http://cmuir.cmu.ac.th/handle/6653943832/4145
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