Small interfering RNAs (siRNAs) are the mediators of mRNA degradation in the process of RNA interference (RNAi). Here, we describe a human biochemical system that recapitulates siRNA-mediated target RNA degradation. By using affinity-tagged siRNAs, we demonstrate that a single-stranded siRNA resides in the RNA-induced silencing complex (RISC) together with eIF2C1 and/or eIF2C2 (human GERp95) Argonaute proteins. RISC is rapidly formed in HeLa cell cytoplasmic extract supplemented with 21 nt siRNA duplexes, but also by adding single-stranded antisense RNAs, which range in size between 19 and 29 nucleotides. Single-stranded antisense siRNAs are also effectively silencing genes in HeLa cells, especially when 5'-phosphorylated, and expand the repertoire of RNA reagents suitable for gene targeting.
机构:
Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002
Bitko V.
Barik S.
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机构:
Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002
机构:
Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002
Bitko V.
Barik S.
论文数: 0引用数: 0
h-index: 0
机构:
Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002Dept. of Biochem. and Molec. Biology, University of South Alabama, College of Medicine, Mobile, AL 36688-0002