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

被引:19
|
作者
Chen, TP
Côté, J
Carvajal, HV
Richard, S
机构
[1] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Terry Fox Mol Oncol Grp, Montreal, PQ H3T 1E2, Canada
[2] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Bloomfield Ctr Res Aging, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[5] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1074/jbc.M102247200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. Fur. thermore, 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.
引用
收藏
页码:30803 / 30811
页数:9
相关论文
共 25 条
  • [21] Genome-Wide Identification of the Glycine-Rich RNA-Binding Protein Genes and Their Expression Analysis upon Aspergillus flavus Infection in Groundnut (Arachis hypogaea)
    Jose, Alin M.
    Tejaswi, Avuthu
    Kokiladevi, Eswaran
    Sharma, Niharika
    Yogendra, Kalenahalli
    AGRONOMY-BASEL, 2024, 14 (01):
  • [22] Genome-wide identification, phylogenetic analysis, and expression profiling of glycine-rich RNA-binding protein (GRPs) genes in seeded and seedless grapes (Vitis vinifera)
    Tang, Yujin
    Huang, Congbo
    Li, Yan
    Wang, Yuejin
    Zhang, Chaohong
    PHYSIOLOGY AND MOLECULAR BIOLOGY OF PLANTS, 2021, 27 (10) : 2231 - 2243
  • [23] Genome-wide identification, phylogenetic analysis, and expression profiling of glycine-rich RNA-binding protein (GRPs) genes in seeded and seedless grapes (Vitis vinifera)
    Yujin Tang
    Congbo Huang
    Yan Li
    Yuejin Wang
    Chaohong Zhang
    Physiology and Molecular Biology of Plants, 2021, 27 : 2231 - 2243
  • [24] Structural insights to the RRM-domain of the glycine-rich RNA-binding protein from Sorghum bicolor and its role in cold stress tolerance in E. coli
    Singh, Harpreet
    Paithankar, Harshad
    Poojari, Chetan S.
    Kaur, Kirandeep
    Singh, Supreet
    Shobhawat, Rahul
    Singh, Prabhjeet
    Kumar, Ashutosh
    Mithu, Venus Singh
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2024, 282
  • [25] Selective DNA-binding of SP120 (rat ortholog of human hnRNP U) is mediated by arginine-glycine rich domain and modulated by RNA
    Miyaji, Mary
    Kawano, Shinji
    Furuta, Ryohei
    Murakami, Emi
    Ikeda, Shogo
    Tsutsui, Kimiko M.
    Tsutsui, Ken
    PLOS ONE, 2023, 18 (08):