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Science ; 370(6523)2020 12 18.
Article in English | MEDLINE | ID: mdl-33184237

ABSTRACT

MicroRNAs (miRNAs) associate with Argonaute (AGO) proteins to direct widespread posttranscriptional gene repression. Although association with AGO typically protects miRNAs from nucleases, extensive pairing to some unusual target RNAs can trigger miRNA degradation. We found that this target-directed miRNA degradation (TDMD) required the ZSWIM8 Cullin-RING E3 ubiquitin ligase. This and other findings support a mechanistic model of TDMD in which target-directed proteolysis of AGO by the ubiquitin-proteasome pathway exposes the miRNA for degradation. Moreover, loss-of-function studies indicated that the ZSWIM8 Cullin-RING ligase accelerates degradation of numerous miRNAs in cells of mammals, flies, and nematodes, thereby specifying the half-lives of most short-lived miRNAs. These results elucidate the mechanism of TDMD and expand its inferred role in shaping miRNA levels in bilaterian animals.


Subject(s)
Argonaute Proteins/metabolism , MicroRNAs/metabolism , RNA Stability , RNA, Long Noncoding/metabolism , Ubiquitin-Protein Ligases/metabolism , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans Proteins/metabolism , Drosophila , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Elongin/genetics , Elongin/metabolism , Gene Knockdown Techniques , Humans , K562 Cells , Mice , NIH 3T3 Cells , Proteolysis , RNA, Long Noncoding/genetics , Ubiquitin-Protein Ligases/genetics
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