POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins

被引:64
作者
Hu, Boqin [1 ,2 ]
Yang, Yu-Cheng T. [1 ,2 ,3 ]
Huang, Yiming [1 ,2 ]
Zhu, Yumin [1 ,2 ]
Lu, Zhi John [1 ,2 ]
机构
[1] Tsinghua Univ, Sch Life Sci, Ctr Synthet & Syst Biol, Ctr Plant Biol,MOE Key Lab Bioinformat, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Sch Life Sci, Tsinghua Peking Joint Ctr Life Sci, Beijing 100084, Peoples R China
[3] Univ Calif Los Angeles, Dept Stat, Los Angeles, CA 90095 USA
基金
中国国家自然科学基金;
关键词
CLEAVAGE FACTOR-I; GENE-EXPRESSION; WIDE ANALYSIS; WEB SERVER; HITS-CLIP; DATABASE; PREDICTION; SITES; TRANSCRIPTOME; VARIANTS;
D O I
10.1093/nar/gkw888
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present POSTAR (http://POSTAR.ncrnalab.org), a resource of POST-trAnscriptional Regulation coordinated by RNA-binding proteins (RBPs). Precise characterization of post-transcriptional regulatory maps has accelerated dramatically in the past few years. Based on new studies and resources, POSTAR supplies the largest collection of experimentally probed (similar to 23 million) and computationally predicted (approximately 117 million) RBP binding sites in the human and mouse transcriptomes. POSTAR annotates every transcript and its RBP binding sites using extensive information regarding various molecular regulatory events (e.g., splicing, editing, and modification), RNA secondary structures, disease-associated variants, and gene expression and function. Moreover, POSTAR provides a friendly, multi-mode, integrated search interface, which helps users to connect multiple RBP binding sites with post-transcriptional regulatory events, phenotypes, and diseases. Based on our platform, we were able to obtain novel insights into post-transcriptional regulation, such as the putative association between CPSF6 binding, RNA structural domains, and Li-Fraumeni syndrome SNPs. In summary, POSTAR represents an early effort to systematically annotate post-transcriptional regulatory maps and explore the putative roles of RBPs in human diseases.
引用
收藏
页码:D104 / D114
页数:11
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