Abstract
Adenosine deaminases that act on RNA (ADARs) are RNA-editing enzymes that deaminate adenosines to create inosines in double-stranded RNA (dsRNA). Here we demonstrate that ADARs are not required for RNA interference (RNAi) and that they do not antagonize the pathway to a detectable level when RNAi is initiated by injecting dsRNA. We find, however, that transgenes expressed in the somatic tissues of wild-type animals are silenced in strains with deletions in the two genes encoding ADARs, adr-1 and adr-2. Transgene-induced gene silencing in adr-1;adr-2 mutants depends on genes required for RNAi, suggesting that a dsRNA intermediate is involved. In wild-type animals we detect edited dsRNA corresponding to transgenes, and we propose that editing of this dsRNA prevents somatic transgenes from initiating RNAi in wild-type animals.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adenosine Deaminase / genetics
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Adenosine Deaminase / metabolism*
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Animals
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Base Sequence
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Caenorhabditis elegans / enzymology*
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Caenorhabditis elegans / genetics*
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Caenorhabditis elegans Proteins / genetics
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Caenorhabditis elegans Proteins / metabolism
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Calmodulin-Binding Proteins / genetics
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Gene Deletion
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Gene Silencing
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Genotype
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Heat-Shock Proteins / genetics
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Muscle Proteins / genetics
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Neurons / enzymology
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Neurons / metabolism
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RNA Editing*
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RNA Interference* / drug effects
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RNA, Double-Stranded / genetics
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RNA, Double-Stranded / metabolism*
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Reverse Transcriptase Polymerase Chain Reaction
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Transgenes / genetics
Substances
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Caenorhabditis elegans Proteins
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Calmodulin-Binding Proteins
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Heat-Shock Proteins
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Muscle Proteins
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RNA, Double-Stranded
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unc-22 protein, C elegans
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Adenosine Deaminase