Integrative analyses shed new light on human ribosomal protein gene regulation

被引:19
|
作者
Li, Xin [1 ]
Zheng, Yiyu [1 ]
Hu, Haiyan [1 ]
Li, Xiaoman [2 ]
机构
[1] Univ Cent Florida, Dept Elect Engn & Comp Sci, Orlando, FL 32816 USA
[2] Univ Cent Florida, Burnett Sch Biomed Sci, Orlando, FL 32816 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家科学基金会;
关键词
TRANSCRIPTION FACTOR; SYSTEMATIC IDENTIFICATION; PROMOTER; GENOME; REVEALS; MOTIF; ELEMENTS; BINDING; MAP; ARCHITECTURE;
D O I
10.1038/srep28619
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ribosomal protein genes (RPGs) are important house-keeping genes that are well-known for their coordinated expression. Previous studies on RPGs are largely limited to their promoter regions. Recent high-throughput studies provide an unprecedented opportunity to study how human RPGs are transcriptionally modulated and how such transcriptional regulation may contribute to the coordinate gene expression in various tissues and cell types. By analyzing the DNase I hypersensitive sites under 349 experimental conditions, we predicted 217 RPG regulatory regions in the human genome. More than 86.6% of these computationally predicted regulatory regions were partially corroborated by independent experimental measurements. Motif analyses on these predicted regulatory regions identified 31 DNA motifs, including 57.1% of experimentally validated motifs in literature that regulate RPGs. Interestingly, we observed that the majority of the predicted motifs were shared by the predicted distal and proximal regulatory regions of the same RPGs, a likely general mechanism for enhancer-promoter interactions. We also found that RPGs may be differently regulated in different cells, indicating that condition-specific RPG regulatory regions still need to be discovered and investigated. Our study advances the understanding of how RPGs are coordinately modulated, which sheds light to the general principles of gene transcriptional regulation in mammals.
引用
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页数:9
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