| Literature DB >> 16179478 |
Florian C Oberstrass1, Sigrid D Auweter, Michèle Erat, Yann Hargous, Anke Henning, Philipp Wenter, Luc Reymond, Batoul Amir-Ahmady, Stefan Pitsch, Douglas L Black, Frédéric H-T Allain.
Abstract
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.Entities:
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Year: 2005 PMID: 16179478 DOI: 10.1126/science.1114066
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728