Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription

被引:18
作者
Bornelov, Susanne [1 ]
Komorowski, Jan [1 ,2 ]
Wadelius, Claes [3 ]
机构
[1] Uppsala Univ, Sci Life Lab, Dept Cell & Mol Biol, SE-75124 Uppsala, Sweden
[2] Polish Acad Sci, Inst Comp Sci, PL-01248 Warsaw, Poland
[3] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, SE-75108 Uppsala, Sweden
来源
BMC GENOMICS | 2015年 / 16卷
基金
瑞典研究理事会;
关键词
Antisense transcription; CTCF; RAD21; Cohesin; CAGE; Epigenetics; Transcription factor; Histone modification; POLYMERASE-II ELONGATION; HUMAN GENOME; DIVERGENT TRANSCRIPTION; NUCLEOSOME ORGANIZATION; NASCENT TRANSCRIPTION; ACTIVE PROMOTERS; DNA METHYLATION; FACTOR-BINDING; HUMAN-CELLS; CHROMATIN;
D O I
10.1186/s12864-015-1485-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Several post-translational histone modifications are mainly found in gene promoters and are associated with the promoter activity. It has been hypothesized that histone modifications regulate the transcription, as opposed to the traditional view with transcription factors as the key regulators. Promoters of most active genes do not only initiate transcription of the coding sequence, but also a substantial amount of transcription of the antisense strand upstream of the transcription start site (TSS). This promoter feature has generally not been considered in previous studies of histone modifications and transcription factor binding. Results: We annotated protein-coding genes as bi- or unidirectional depending on their mode of transcription and compared histone modifications and transcription factor occurrences between them. We found that H3K4me3, H3K9ac, and H3K27ac were significantly more enriched upstream of the TSS in bidirectional genes compared with the unidirectional ones. In contrast, the downstream histone modification signals were similar, suggesting that the upstream histone modifications might be a consequence of transcription rather than a cause. Notably, we found well-positioned CTCF and RAD21 peaks approximately 60-80 bp upstream of the TSS in the unidirectional genes. The peak heights were related to the amount of antisense transcription and we hypothesized that CTCF and cohesin act as a barrier against antisense transcription. Conclusions: Our results provide insights into the distribution of histone modifications at promoters and suggest a novel role of CTCF and cohesin as regulators of transcriptional direction.
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页数:13
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