Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.

As a first step towards discovery of genes expressed from only one allele in the CNS, we used a tiling array assay for DNA sequences that are both methylated and unmethylated (the MAUD assay). We analyzed regulatory regions of the entire mouse brain transcriptome, and found that approximately 10% of...

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Main Authors: Jinhui Wang, Zuzana Valo, Chauncey W Bowers, David D Smith, Zheng Liu, Judith Singer-Sam
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-11-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2973945?pdf=render
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author Jinhui Wang
Zuzana Valo
Chauncey W Bowers
David D Smith
Zheng Liu
Judith Singer-Sam
author_facet Jinhui Wang
Zuzana Valo
Chauncey W Bowers
David D Smith
Zheng Liu
Judith Singer-Sam
author_sort Jinhui Wang
collection DOAJ
description As a first step towards discovery of genes expressed from only one allele in the CNS, we used a tiling array assay for DNA sequences that are both methylated and unmethylated (the MAUD assay). We analyzed regulatory regions of the entire mouse brain transcriptome, and found that approximately 10% of the genes assayed showed dual DNA methylation patterns. They include a large subset of genes that display marks of both active and silent, i.e., poised, chromatin during development, consistent with a link between differential DNA methylation and lineage-specific differentiation within the CNS. Sixty-five of the MAUD hits and 57 other genes whose function is of relevance to CNS development and/or disorders were tested for allele-specific expression in F(1) hybrid clonal neural stem cell (NSC) lines. Eight MAUD hits and one additional gene showed such expression. They include Lgi1, which causes a subtype of inherited epilepsy that displays autosomal dominance with incomplete penetrance; Gfra2, a receptor for glial cell line-derived neurotrophic factor GDNF that has been linked to kindling epilepsy; Unc5a, a netrin-1 receptor important in neurodevelopment; and Cspg4, a membrane chondroitin sulfate proteoglycan associated with malignant melanoma and astrocytoma in human. Three of the genes, Camk2a, Kcnc4, and Unc5a, show preferential expression of the same allele in all clonal NSC lines tested. The other six genes show a stochastic pattern of monoallelic expression in some NSC lines and bi-allelic expression in others. These results support the estimate that 1-2% of genes expressed in the CNS may be subject to allelic exclusion, and demonstrate that the group includes genes implicated in major disorders of the CNS as well as neurodevelopment.
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spelling doaj.art-5069f7d5324648e3abdd1fa1e9c97e0e2022-12-21T23:23:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-11-01511e1384310.1371/journal.pone.0013843Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.Jinhui WangZuzana ValoChauncey W BowersDavid D SmithZheng LiuJudith Singer-SamAs a first step towards discovery of genes expressed from only one allele in the CNS, we used a tiling array assay for DNA sequences that are both methylated and unmethylated (the MAUD assay). We analyzed regulatory regions of the entire mouse brain transcriptome, and found that approximately 10% of the genes assayed showed dual DNA methylation patterns. They include a large subset of genes that display marks of both active and silent, i.e., poised, chromatin during development, consistent with a link between differential DNA methylation and lineage-specific differentiation within the CNS. Sixty-five of the MAUD hits and 57 other genes whose function is of relevance to CNS development and/or disorders were tested for allele-specific expression in F(1) hybrid clonal neural stem cell (NSC) lines. Eight MAUD hits and one additional gene showed such expression. They include Lgi1, which causes a subtype of inherited epilepsy that displays autosomal dominance with incomplete penetrance; Gfra2, a receptor for glial cell line-derived neurotrophic factor GDNF that has been linked to kindling epilepsy; Unc5a, a netrin-1 receptor important in neurodevelopment; and Cspg4, a membrane chondroitin sulfate proteoglycan associated with malignant melanoma and astrocytoma in human. Three of the genes, Camk2a, Kcnc4, and Unc5a, show preferential expression of the same allele in all clonal NSC lines tested. The other six genes show a stochastic pattern of monoallelic expression in some NSC lines and bi-allelic expression in others. These results support the estimate that 1-2% of genes expressed in the CNS may be subject to allelic exclusion, and demonstrate that the group includes genes implicated in major disorders of the CNS as well as neurodevelopment.http://europepmc.org/articles/PMC2973945?pdf=render
spellingShingle Jinhui Wang
Zuzana Valo
Chauncey W Bowers
David D Smith
Zheng Liu
Judith Singer-Sam
Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
PLoS ONE
title Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
title_full Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
title_fullStr Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
title_full_unstemmed Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
title_short Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes.
title_sort dual dna methylation patterns in the cns reveal developmentally poised chromatin and monoallelic expression of critical genes
url http://europepmc.org/articles/PMC2973945?pdf=render
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