Structure of PTB bound to RNA: Specific binding and implications for splicing regulation

被引:376
作者
Oberstrass, FC
Auweter, SD
Erat, M
Hargous, Y
Henning, A
Wenter, P
Reymond, L
Amir-Ahmady, B
Pitsch, S
Black, DL
Allain, FHT [1 ]
机构
[1] ETH Honggerberg, Swiss Fed Inst Technol, Dept Biol, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
[2] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[4] EPFL, Lab Nucl Acid Chem LCAN, CH-1015 Lausanne, Switzerland
[5] Mol LIfe Sci PhD Program, Zurich, Switzerland
关键词
D O I
10.1126/science.1114066
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
The polypyrimidine tract binding protein (PTB) is a 58-kilodalton RNA binding protein involved in multiple aspects of messenger RNA metabolism, including the repression of alternative exons. We have determined the solution structures of the four RNA binding domains (RBDs) of PTB, each bound to a CUCUCU oligonucleotide. Each RBD binds RNA with a different binding specificity. RBD3 and RBD4 interact, resulting in an antiparallel orientation of their bound RNAs. Thus, PTB will induce RNA looping when bound to two separated pyrimidine tracts within the same RNA. This leads to structural models for how PTB functions as an alternative-splicing repressor.
引用
收藏
页码:2054 / 2057
页数:4
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