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Cell Rep ; 25(8): 2273-2284.e3, 2018 11 20.
Artigo em Inglês | MEDLINE | ID: mdl-30463021

RESUMO

The dynamic process by which nuclear RNAi engages a transcriptionally active target, before the repressive state is stably established, remains largely a mystery. Here, we found that the onset of exogenous dsRNA-induced nuclear RNAi in C. elegans is a transgenerational process, and it requires a putative histone methyltransferase (HMT), SET-32. By developing a CRISPR-based genetic approach, we found that silencing establishment at the endogenous targets of germline nuclear RNAi also requires SET-32. Although SET-32 and two H3K9 HMTs, MET-2 and SET-25, are dispensable for the maintenance of silencing, they do contribute to transcriptional repression in mutants that lack the germline nuclear Argonaute protein HRDE-1, suggesting a conditional role of heterochromatin in the maintenance phase. Our study indicates that (1) establishment and maintenance of siRNA-guided transcriptional repression are two distinct processes with different genetic requirements and (2) the rate-limiting step of the establishment phase is a transgenerational, chromatin-based process.


Assuntos
Proteínas de Caenorhabditis elegans/fisiologia , Caenorhabditis elegans/genética , Epigênese Genética , Heterocromatina/metabolismo , Histona Metiltransferases/fisiologia , Interferência de RNA , Animais , Sistemas CRISPR-Cas/genética , Proteínas de Caenorhabditis elegans/genética , Células Germinativas/metabolismo , Histona Metiltransferases/genética , Histonas/metabolismo , Lisina/metabolismo , Mutação/genética , RNA de Cadeia Dupla/metabolismo , Transcrição Gênica
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