Unique repression domains of Pumilio utilize deadenylation and decapping factors to accelerate destruction of target mRNAs

René M. Arvola, Chung Te Chang, Joseph P. Buytendorp, Yevgen Levdansky, Eugene Valkov, Peter L. Freddolino, Aaron C. Goldstrohm

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Pumilio is an RNA-binding protein that represses a network of mRNAs to control embryogenesis, stem cell fate, fertility and neurological functions in Drosophila. We sought to identify the mechanism of Pumilio-mediated repression and find that it accelerates degradation of target mRNAs, mediated by three N-terminal Repression Domains (RDs), which are unique to Pumilio orthologs. We show that the repressive activities of the Pumilio RDs depend on specific subunits of the Ccr4-Not (CNOT) deadenylase complex. Depletion of Pop2, Not1, Not2, or Not3 subunits alleviates Pumilio RD-mediated repression of protein expression and mRNA decay, whereas depletion of other CNOT components had little or no effect. Moreover, the catalytic activity of Pop2 deadenylase is important for Pumilio RD activity. Further, we show that the Pumilio RDs directly bind to the CNOT complex. We also report that the decapping enzyme, Dcp2, participates in repression by the N-terminus of Pumilio. These results support a model wherein Pumilio utilizes CNOT deadenylase and decapping complexes to accelerate destruction of target mRNAs. Because the N-terminal RDs are conserved in mammalian Pumilio orthologs, the results of this work broadly enhance our understanding of Pumilio function and roles in diseases including cancer, neurodegeneration and epilepsy.

Original languageEnglish (US)
Pages (from-to)1843-1871
Number of pages29
JournalNucleic acids research
Volume48
Issue number4
DOIs
StatePublished - Feb 28 2020

Bibliographical note

Funding Information:
National Institute of General Medical Sciences, National Institutes of Health [R01GM105707 to A.C.G.]; National Science Foundation [DGE 1256260 to R.M.A.]; University of Michigan Genetics Training Program [NRSA 5T32GM007544 to R.M.A.]; Max Planck Society (to E.V.); National Institute of General Medical Sciences, National Institutes of Health [R35GM128637 to P.F.]. Funding for open access charge: University of Minnesota institutional funds. Conflict of interest statement. None declared.

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