Arginine-serine-rich domains bound at splicing enhancers contact the branchpoint to promote prespliceosome assembly
Shen, Haihong ; Kan, Julie L. C. ; Green, Michael R.
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Keywords
Base Sequence
Binding Sites
Enhancer Elements, Genetic
Hela Cells
Humans
Molecular Sequence Data
Protein Binding
Protein Structure, Tertiary
RNA Splicing
RNA, Messenger
RNA-Binding Proteins
Recombinant Fusion Proteins
Serine
Spliceosomes
Biochemistry, Biophysics, and Structural Biology
Genetics and Genomics
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Abstract
Exonic splicing enhancers (ESEs) are required for splicing of certain pre-mRNAs and function by providing binding sites for serine-arginine (SR) proteins, which contain an arginine-serine-rich (RS) domain. How an RS domain bound at the ESE promotes splicing is poorly understood. We have developed an RNA-protein crosslinking procedure to identify the target of the ESE-bound RS domain. Using this approach, we show that the ESE-bound RS domain specifically contacts the pre-mRNA branchpoint. The interaction between the ESE-bound RS domain and the branchpoint occurs in the prespliceosome and is dependent upon the same splicing signals, biochemical factors, and reaction conditions required to support prespliceosome assembly. Analysis of RS domain mutants demonstrates that the ability to interact with the branchpoint, to promote prespliceosome assembly, and to support splicing are related activities. We conclude that the ESE-bound RS domain functions by contacting the branchpoint to promote prespliceosome assembly.
Source
Mol Cell. 2004 Feb 13;13(3):367-76.