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Science 23 September 2005:
Vol. 309. no. 5743, pp. 2054 - 2057
DOI: 10.1126/science.1114066

Reports

Structure of PTB Bound to RNA: Specific Binding and Implications for Splicing Regulation

Florian C. Oberstrass,1,4* Sigrid D. Auweter,1,4* Michèle Erat,1* Yann Hargous,1 Anke Henning,1 Philipp Wenter,3 Luc Reymond,3 Batoul Amir-Ahmady,2 Stefan Pitsch,3 Douglas L. Black,2 Frédéric H.-T. Allain1{ddagger}

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.

1 Institute for Molecular Biology and Biophysics, Department of Biology, Swiss Federal Institute of Technology, Zürich, ETH-Hönggerberg, CH-8093 Zürich, Switzerland.
2 Department of Microbiology, Immunology, and Molecular Genetics and Howard Hughes Medical Institute, University of California Los Angeles, Los Angeles, CA 90095, USA.
3 Laboratory of Nucleic Acid Chemistry LCAN-EPFL, Lausanne, Switzerland.
4 Molecular Life Science Ph.D. Program, Zürich, Switzerland.

* These authors contributed equally to this work.

{ddagger} To whom correspondence should be addressed. E-mail: allain{at}mol.biol.ethz.ch

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Science. ISSN 0036-8075 (print), 1095-9203 (online)