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Abstract

MicroRNAs (miRNAs) are genome-encoded ~22 nucleotide-long RNAs that silence gene expression post-transcriptionally by base pairing with the 3’ untranslated regions of target mRNAs. To exert their func- tion, miRNAs associate with Argonaute proteins (AGOs) in miRNA- induced silencing complexes (miRISCs), which silence the expression of mRNAs containing partially or fully complementary miRNA-binding sites. In animals, most miRNAs are only partially complementary to their targets. In this case, our group has shown that the AGO proteins are not sufficient to mediate silencing and require interaction with pro- teins of the GW182 family. We have also shown that AGO-GW182 complexes mediate silencing by promoting translational repression and mRNA deadenylation catalyzed by CAF1-CCR4-NOT, the major cytoplasmic deadenylase complex. Deadenylation decreases translation efficiency and, in somatic cells, commits the mRNA to decapping and 5’-to-3’ exonucleolytic degradation. Our analysis of GW182 pro- tein function has revealed two domains critical for silencing: an N-ter- minal GW-repeat-containing region conferring binding to AGOs, and a bipartite silencing domain, consisting of Mid and C-terminal regions, which elicits translational repression and degradation of miRNA tar- gets. Exactly how the bipartite silencing domain of GW182 proteins interferes with translation and accelerates deadenylation is not com- pletely understood. We have recently started to address this ques- tion by showing that the silencing domains of GW182 interact with the cytoplasmic poly(A)-binding protein 1 (PABPC1), suggesting GW182 proteins are PABP-interacting proteins (Paips) that interfere with the function of PABPC1 in translation and mRNA stabilization.