A proteomic study of TAR-RNA binding protein (TRBP)-associated factors

被引:20
|
作者
Chi, Ya-Hui [1 ,2 ]
Semmes, Oliver John [3 ]
Jeang, Kuan-Teh [1 ]
机构
[1] NIAID, NIH, Mol Virol Sect, Mol Microbiol Lab, Bethesda, MD 20892 USA
[2] Natl Hlth Res Inst, Inst Cellular & Syst Med, Zhunan, Taiwan
[3] Eastern Virginia Med Sch, Leroy T Canoles Jr Canc Res Ctr, Dept Microbiol & Mol Cell Biol, Norfolk, VA 23501 USA
来源
CELL AND BIOSCIENCE | 2011年 / 1卷
关键词
HIV-1; REPLICATION; KINASE PKR; TRBP; DICER; EXPRESSION; MICRORNAS; INTERFERENCE; SUPPRESSION; VIRUSES; MIRNAS;
D O I
10.1186/2045-3701-1-9
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
Background: The human TAR RNA-binding protein, TRBP, was first identified and cloned based on its high affinity binding to the small hairpin trans-activation responsive (TAR) RNA of HIV-1. TRBP has more recently been found to be a constituent of the RNA-induced silencing complex (RISC) serving as a Dicer co-factor in the processing of the similar to 70 nucleotide pre-microRNAs(miRNAs) to 21-25 nucleotide mature miRNAs. Findings: Using co-immunoprecipitation and protein-identification by mass spectrometry, we characterized intracellular proteins that complex with TRBP. These interacting proteins include those that have been described to act in protein synthesis, RNA modifications and processing, DNA transcription, and cell proliferation. Conclusions: Our findings provide a proteome of factors that may cooperate with TRBP in activities such as miRNA processing and in RNA interference by the RISC complex.
引用
收藏
页数:5
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