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Insect Biochem Mol Biol ; 33(9): 949-57, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12915186

ABSTRACT

Introduction of double stranded RNA into invertebrate cells often results in posttranscriptional silencing of target genes through a mechanism termed RNA interference (RNAi). Double-stranded RNA is cleaved by an RNAse III-like enzyme, termed dicer, to small interfering RNAs (siRNAs). In Drosophila, these siRNAs are incorporated in the RNA induced silencing complex (RISC) and mediate degradation of target mRNA. The RISC complex contains members of Argonaute (Ago) family of proteins. We show here that RNAi in a hemocyte cell line of Anopheles gambiae, the principal malaria vector in Africa, requires expression of dicer-2, Ago2 and Ago3 proteins. Furthermore, we demonstrate that RNAi in the mosquito does not spread outside of the target region, suggesting that RNA dependent RNA polymerase mediated transitive amplification is absent in the mosquito.


Subject(s)
Anopheles/genetics , RNA Interference/physiology , Animals , Cell Line , Gene Silencing/physiology , Genes, Insect/genetics , Luciferases/genetics , Phylogeny , Plasmids/genetics , Protein Biosynthesis/genetics , RNA, Double-Stranded/genetics , RNA, Double-Stranded/metabolism , RNA, Double-Stranded/pharmacology , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/metabolism , RNA-Induced Silencing Complex/genetics , RNA-Induced Silencing Complex/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Ribonuclease III/genetics , Ribonuclease III/metabolism , Transfection
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