Genome-wide Analysis of Alternative Pre-mRNA Splicing and RNA-Binding Specificities of the Drosophila hnRNP A/B Family Members

被引:70
作者
Blanchette, Marco [1 ,2 ]
Green, Richard E. [1 ,3 ]
MacArthur, Stewart [4 ]
Brooks, Angela N. [1 ]
Brenner, Steven E. [1 ,2 ,3 ]
Eisen, Michael B. [1 ,4 ]
Rio, Donald C. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Ctr Integrat Genom, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[4] Ernest Orlando Lawrence Berkeley Natl Lab, Dept Genome Sci, Div Life Sci, Berkeley, CA 94720 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENE-EXPRESSION; IN-VIVO; PROTEINS; SITES; SELECTION; A1; OVEREXPRESSION; TRANSCRIPTION; MODULATION; MUTATIONS;
D O I
10.1016/j.molcel.2009.01.022
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
Heterogeneous nuclear ribonucleoproteins (hnRNPs) have been traditionally seen as proteins packaging RNA nonspecifically into ribonucleoprotein particles (RNPs), but evidence suggests specific cellular functions on discrete target pre-mRNAs. Here we report genome-wide analysis of alternative splicing patterns regulated by four Drosophila homologs of the mammalian hnRNP A/B family (hrp36, hrp38, hrp40, and hrp48). Analysis of the global RNA-binding distributions of each protein revealed both small and extensively bound regions on target transcripts. A significant subset of RNAs were bound and regulated by more than one hnRNP protein, revealing a combinatorial network of interactions. In vitro RNA-binding site selection experiments (SELEX) identified distinct binding motif specificities for each protein, which were overrepresented in their respective regulated and bound transcripts. These results indicate that individual heterogeneous ribonucleoproteins have specific affinities for overlapping, but distinct, populations of target pre-mRNAs controlling their patterns of RNA processing.
引用
收藏
页码:438 / 449
页数:12
相关论文
共 53 条
[41]  
PINOLROMA S, 1990, METHOD ENZYMOL, V181, P326
[42]   EXON SKIPPING BY OVEREXPRESSION OF A DROSOPHILA HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN IN-VIVO [J].
SHEN, J ;
ZU, K ;
CASS, CL ;
BEYER, AL ;
HIRSH, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :1822-1825
[43]   Alternative pre-mRNA splicing:: the logic of combinatorial control [J].
Smith, CWJ ;
Valcárcel, J .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (08) :381-388
[44]   An RNA map predicting Nova-dependent splicing regulation [J].
Ule, Jernej ;
Stefani, Giovanni ;
Mele, Aldo ;
Ruggiu, Matteo ;
Wang, Xuning ;
Taneri, Bahar ;
Gaasterland, Terry ;
Blencowe, Benjamin J. ;
Darnell, Robert B. .
NATURE, 2006, 444 (7119) :580-586
[45]   Alternative isoform regulation in human tissue transcriptomes [J].
Wang, Eric T. ;
Sandberg, Rickard ;
Luo, Shujun ;
Khrebtukova, Irina ;
Zhang, Lu ;
Mayr, Christine ;
Kingsmore, Stephen F. ;
Schroth, Gary P. ;
Burge, Christopher B. .
NATURE, 2008, 456 (7221) :470-476
[46]   General and specific functions of exonic splicing silencers in splicing control [J].
Wang, Zefeng ;
Xiao, Xinshu ;
Van Nostrand, Eric ;
Burge, Christopher B. .
MOLECULAR CELL, 2006, 23 (01) :61-70
[47]   SC35 and heterogeneous nuclear ribonucleoprotein A/B proteins bind to a juxtaposed exonic splicing enhancer/exonic splicing silencer element to regulate HIV-1 tat exon 2 splicing [J].
Zahler, AM ;
Damgaard, CK ;
Kjems, J ;
Caputi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :10077-10084
[48]   Whole-genome ChIP-chip analysis of Dorsal, Twist, and Snail suggests integration of diverse patterning processes in the Drosophila embryo [J].
Zeitlinger, Julia ;
Zinzen, Robert P. ;
Stark, Alexander ;
Kellis, Manolis ;
Zhang, Hailan ;
Young, Richard A. ;
Levine, Michael .
GENES & DEVELOPMENT, 2007, 21 (04) :385-390
[49]   Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2 [J].
Zhang, Chaolin ;
Zhang, Zuo ;
Castle, John ;
Sun, Shuying ;
Johnson, Jason ;
Krainer, Adrian R. ;
Zhang, Michael Q. .
GENES & DEVELOPMENT, 2008, 22 (18) :2550-2563
[50]   Exon identity established through differential antagonism between exonic splicing silencer-bound hnRNP A1 and enhancer-bound SR proteins [J].
Zhu, J ;
Mayeda, A ;
Krainer, AR .
MOLECULAR CELL, 2001, 8 (06) :1351-1361