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PMID: 11395494 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification of Sam68 arginine glycine-rich sequences capable of conferring nonspecific RNA binding to the GSG domain.

The Journal of biological chemistry ·Vol. 276 ·No. 33 ·2001-08-17 ·Pages 30803-11

Chen T, Côté J, Carvajal HV, Richard S

Abstract

Sam68 is an RNA-binding protein that contains a heterogeneous nuclear ribonucleoprotein K homology domain embedded in a larger RNA binding domain called the GSG (GRP33, Sam68, GLD-1) domain. This family of proteins is often referred to as the STAR (signal transduction and activators of RNA metabolism) proteins. It is not known whether Sam68 is a general nonspecific RNA-binding protein or whether it recognizes specific response elements in mRNAs with high affinity. Sam68 has been shown to bind homopolymeric RNA and a synthetic RNA sequence called G8-5 that has a core UAAA motif. Here we performed a structure function analysis of Sam68 and identified two arginine glycine (RG)-rich regions that confer nonspecific RNA binding to the Sam68 GSG domain. In addition, by using chimeric proteins between Sam68 and QKI-7, we demonstrated that one of the Sam68 RG-rich sequences of 26 amino acids was sufficient to confer homopolymeric RNA binding to the GSG domain of QKI-7, another STAR protein. Furthermore, that minimal sequence can also give QKI-7 the ability (as Sam68) to functionally substitute for HIV-1 REV to facilitate the nuclear export of RNAs. Our studies suggest that neighboring RG-rich sequences may impose nonspecific RNA binding to GSG domains. Because the Sam68 RNA binding activity is negatively regulated by tyrosine phosphorylation, our data lead us to propose that Sam68 might be a specific RNA-binding protein when tyrosine phosphorylated.

MeSH Terms
Amino Acid Sequence Molecular Sequence Data Phosphorylation Poly U/metabolism RNA/metabolism RNA-Binding Proteins/chemistry,metabolism Recombinant Fusion Proteins/metabolism Repetitive Sequences, Amino Acid
Chemicals
RNA-Binding Proteins Recombinant Fusion Proteins Poly U RNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chen T
Terry Fox Molecular Oncology Group and the Bloomfield Center for Research on Aging, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, Canada.
Côté J
Carvajal H V
Richard S
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-08-17
Epub
2001-00-06
Pages
30803-11
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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