RISE: a database of RNA interactome from sequencing experiments

被引:81
作者
Gong, Jing [1 ,2 ]
Shao, Di [1 ,2 ]
Xu, Kui [1 ,2 ]
Lu, Zhipeng [3 ]
Lu, Zhi John [1 ]
Yang, Yucheng T. [4 ]
Zhang, Qiangfeng Cliff [1 ,2 ]
机构
[1] Tsinghua Univ, MOE Key Lab Bioinformat, Ctr Synthet & Syst Biol, Tsinghua Peking Joint Ctr Life Sci,Sch Life Sci, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Beijing Adv Innovat Ctr Struct Biol, Beijing 100084, Peoples R China
[3] Stanford Univ, Ctr Personal Dynam Regulomes, Stanford, CA 94305 USA
[4] 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
NONCODING RNAS; IN-VIVO; REVEALS; RESOURCE; PRINCIPLES; NETWORK; GENE;
D O I
10.1093/nar/gkx864
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 RISE (http://rise.zhanglab.net), a database of RNA Interactome from Sequencing Experiments. RNA-RNA interactions (RRIs) are essential for RNA regulation and function. RISE provides a comprehensive collection of RRIs that mainly come from recent transcriptome-wide sequencing-based experiments like PARIS, SPLASH, LIGR-seq, and MARIO, as well as targeted studies like RIA-seq, RAP-RNA and CLASH. It also includes interactions aggregated from other primary databases and publications. The RISE database currently contains 328,811 RNA-RNA interactions mainly in human, mouse and yeast. While most existing RNA databases mainly contain interactions of miRNA targeting, notably, more than half of the RRIs in RISE are among mRNA and long non-coding RNAs. We compared different RRI datasets in RISE and found limited overlaps in interactions resolved by different techniques and in different cell lines. It may suggest technology preference and also dynamic natures of RRIs. We also analyzed the basic features of the human and mouse RRI networks and found that they tend to be scale-free, small-world, hierarchical and modular. The analysis may nominate important RNAs or RRIs for further investigation. Finally, RISE provides a Circos plot and several table views for integrative visualization, with extensive molecular and functional annotations to facilitate exploration of biological functions for any RRI of interest.
引用
收藏
页码:D194 / D201
页数:8
相关论文
共 43 条
[1]  
[Anonymous], 2008, P 7 PYTHON SCI C
[2]   In Vivo Mapping of Eukaryotic RNA Interactomes Reveals Principles of Higher-Order Organization and Regulation [J].
Aw, Jong Ghut Ashley ;
Shen, Yang ;
Wilm, Andreas ;
Sun, Miao ;
Lim, Xin Ni ;
Boon, Kum-Loong ;
Tapsin, Sidika ;
Chan, Yun-Shen ;
Tan, Cheng-Peow ;
Sim, Adelene Y. L. ;
Zhang, Tong ;
Susanto, Teodorus Theo ;
Fu, Zhiyan ;
Nagarajan, Niranjan ;
Wan, Yue .
MOLECULAR CELL, 2016, 62 (04) :603-617
[3]   Network biology:: Understanding the cell's functional organization [J].
Barabási, AL ;
Oltvai, ZN .
NATURE REVIEWS GENETICS, 2004, 5 (02) :101-U15
[4]   Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses [J].
Cabili, Moran N. ;
Trapnell, Cole ;
Goff, Loyal ;
Koziol, Magdalena ;
Tazon-Vega, Barbara ;
Regev, Aviv ;
Rinn, John L. .
GENES & DEVELOPMENT, 2011, 25 (18) :1915-1927
[5]   Deciphering the rules of ceRNA networks [J].
Cesana, Marcella ;
Daley, George Q. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (18) :7112-7113
[6]   Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity [J].
Chang, Matthew T. ;
Asthana, Saurabh ;
Gao, Sizhi Paul ;
Lee, Byron H. ;
Chapman, Jocelyn S. ;
Kandoth, Cyriac ;
Gao, JianJiong ;
Socci, Nicholas D. ;
Solit, David B. ;
Olshen, Adam B. ;
Schultz, Nikolaus ;
Taylor, Barry S. .
NATURE BIOTECHNOLOGY, 2016, 34 (02) :155-+
[7]   STAR: ultrafast universal RNA-seq aligner [J].
Dobin, Alexander ;
Davis, Carrie A. ;
Schlesinger, Felix ;
Drenkow, Jorg ;
Zaleski, Chris ;
Jha, Sonali ;
Batut, Philippe ;
Chaisson, Mark ;
Gingeras, Thomas R. .
BIOINFORMATICS, 2013, 29 (01) :15-21
[8]   An integrated encyclopedia of DNA elements in the human genome [J].
Dunham, Ian ;
Kundaje, Anshul ;
Aldred, Shelley F. ;
Collins, Patrick J. ;
Davis, CarrieA. ;
Doyle, Francis ;
Epstein, Charles B. ;
Frietze, Seth ;
Harrow, Jennifer ;
Kaul, Rajinder ;
Khatun, Jainab ;
Lajoie, Bryan R. ;
Landt, Stephen G. ;
Lee, Bum-Kyu ;
Pauli, Florencia ;
Rosenbloom, Kate R. ;
Sabo, Peter ;
Safi, Alexias ;
Sanyal, Amartya ;
Shoresh, Noam ;
Simon, Jeremy M. ;
Song, Lingyun ;
Trinklein, Nathan D. ;
Altshuler, Robert C. ;
Birney, Ewan ;
Brown, James B. ;
Cheng, Chao ;
Djebali, Sarah ;
Dong, Xianjun ;
Dunham, Ian ;
Ernst, Jason ;
Furey, Terrence S. ;
Gerstein, Mark ;
Giardine, Belinda ;
Greven, Melissa ;
Hardison, Ross C. ;
Harris, Robert S. ;
Herrero, Javier ;
Hoffman, Michael M. ;
Iyer, Sowmya ;
Kellis, Manolis ;
Khatun, Jainab ;
Kheradpour, Pouya ;
Kundaje, Anshul ;
Lassmann, Timo ;
Li, Qunhua ;
Lin, Xinying ;
Marinov, Georgi K. ;
Merkel, Angelika ;
Mortazavi, Ali .
NATURE, 2012, 489 (7414) :57-74
[9]   A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome [J].
Dusl, Marina ;
Senderek, Jan ;
Mueller, Juliane S. ;
Vogel, Johannes G. ;
Pertl, Anja ;
Stucka, Rolf ;
Lochmueller, Hanns ;
David, Robert ;
Abicht, Angela .
HUMAN MOLECULAR GENETICS, 2015, 24 (12) :3418-3426
[10]   RNA-RNA Interactions Enable Specific Targeting of Noncoding RNAs to Nascent Pre-mRNAs and Chromatin Sites [J].
Engreitz, Jesse M. ;
Sirokman, Klara ;
McDonel, Patrick ;
Shishkin, Alexander A. ;
Surka, Christine ;
Russell, Pamela ;
Grossman, Sharon R. ;
Chow, Amy Y. ;
Guttman, Mitchell ;
Lander, Eric S. .
CELL, 2014, 159 (01) :188-199