AUF1 promotes let-7b loading on argonaute 2

Abstract

Eukaryotic gene expression is tightly regulated post-transcriptionally by RNA-binding proteins (RBPs) and micro- RNAs. The RBP AU-rich-binding factor 1 (AUF1) isoform p37 was found to have high affinity for the micro- RNA let-7b in vitro (Kd = ∼6 nM) in cells. Ribonucleoprotein immunoprecipitation, in vitro association, and single-molecule-binding analyses revealed that AUF1 promoted let-7b loading onto Argonaute 2 (AGO2), the catalytic component of the RNA-induced silencing complex (RISC). In turn, AGO2–let-7 triggered target mRNA decay. Our findings uncover a novel mechanism by which AUF1 binding and transfer of microRNA let-7 to AGO2facilitates let-7-elicited gene silencing.