The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease
Language: 
English
Abstract: 

Huntington's disease (HD) is an autosomal-dominant neurodegenerative disorder resulting from expansion of CAG repeats in the Huntingtin (HTT) gene. Previous studies have shown mutant HTT can alter expression of genes associated with dysregulated epigenetic modifications. One of the most widely studied chromatin modifications is trimethylated lysine 4 of histone 3 (H3K4me3). Here, we conducted the first comprehensive study of H3K4me3 ChIP-sequencing in neuronal chromatin from the prefrontal cortex of six HD cases and six non-neurologic controls, and its association with gene expression measured by RNA-sequencing. We detected 2,830 differentially enriched H3K4me3 peaks between HD and controls, with 55% of them down-regulated in HD. Although H3K4me3 signals are expected to be associated with mRNA levels, we found an unexpected discordance between altered H3K4me3 peaks and mRNA levels. Gene ontology (GO) term enrichment analysis of the genes with differential H3K4me3 peaks, revealed statistically significantly enriched GO terms only in the genes with down-regulated signals in HD. The most frequently implicated biological process terms are organ morphogenesis and positive regulation of gene expression. More than 9,000 H3K4me3 peaks were located not near any recognized transcription start sites and approximately 36% of these "distal" peaks co-localized to known enhancer sites. Six transcription factors and chromatin remodelers are differentially enriched in HD H3K4me3 distal peaks, including EZH2 and SUZ12, two core subunits of the polycomb repressive complex 2 (PRC2). Moreover, PRC2 repressive state was significantly depleted in HD-enriched peaks, suggesting the epigenetic role of PRC2 inhibition associated with up-regulated H3K4me3 in Huntington's disease. In summary, our study provides new insights into transcriptional dysregulation of Huntington's disease by analyzing the differentiation of H3K4me3 enrichment.

Author(s): 
Dong, Xianjun
Tsuji, Junko
Labadorf, Adam
Roussos, Panos
Chen, Jiang-Fan
Myers, Richard H.
Akbarian, Schahram
Weng, Zhiping
Item Type: 
Journal Article
Publication Title: 
PloS One
Journal Abbreviation: 
PLoS ONE
Publication Date: 
2015
Publication Year: 
2015
Pages: 
e0144398
Volume: 
10
Issue: 
12
ISSN: 
1932-6203
DOI: 
10.1371/journal.pone.0144398
Library Catalog: 
PubMed
Extra: 
PMID: 26636336 PMCID: PMC4670094

Turabian/Chicago Citation

Xianjun Dong, Junko Tsuji, Adam Labadorf, Panos Roussos, Jiang-Fan Chen, Richard H. Myers, Schahram Akbarian and Zhiping Weng. 2015. "The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease." PloS One 10: 12: e0144398. 10.1371/journal.pone.0144398.

Wikipedia Citation

<ref> {{Cite journal | doi = 10.1371/journal.pone.0144398 | issn = 1932-6203 | volume = 10 | pages = e0144398 | last = Dong | first = Xianjun | coauthors = Tsuji, Junko, Labadorf, Adam, Roussos, Panos, Chen, Jiang-Fan, Myers, Richard H., Akbarian, Schahram, Weng, Zhiping | title = The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease | journal = PloS One | date = 2015 | pmid = | pmc = }} </ref>