Regulated dicing of pre-mir-144 via reshaping of its terminal loop

Author:

Shang Renfu1,Kretov Dmitry A2,Adamson Scott I3,Treiber Thomas4,Treiber Nora4,Vedanayagam Jeffrey1,Chuang Jeffrey H3,Meister Gunter4,Cifuentes Daniel2,Lai Eric C1ORCID

Affiliation:

1. Developmental Biology Program, Sloan Kettering Institute , 1275 York Ave, Box 252, New York, NY 10065, USA

2. Department of Biochemistry, Boston University School of Medicine , Boston, MA 02118, USA

3. The Jackson Laboratory for Genomic Medicine , Farmington, CT 06032, USA

4. Regensburg Center for Biochemistry (RCB), Laboratory for RNA Biology, University of Regensburg , 93053 Regensburg, Germany

Abstract

Abstract Although the route to generate microRNAs (miRNAs) is often depicted as a linear series of sequential and constitutive cleavages, we now appreciate multiple alternative pathways as well as diverse strategies to modulate their processing and function. Here, we identify an unusually profound regulatory role of conserved loop sequences in vertebrate pre-mir-144, which are essential for its cleavage by the Dicer RNase III enzyme in human and zebrafish models. Our data indicate that pre-mir-144 dicing is positively regulated via its terminal loop, and involves the ILF3 complex (NF90 and its partner NF45/ILF2). We provide further evidence that this regulatory switch involves reshaping of the pre-mir-144 apical loop into a structure that is appropriate for Dicer cleavage. In light of our recent findings that mir-144 promotes the nuclear biogenesis of its neighbor mir-451, these data extend the complex hierarchy of nuclear and cytoplasmic regulatory events that can control the maturation of clustered miRNAs.

Funder

NIH

Susan and Peter Solomon Divisional Genomics Program

M.S.K. Core

Publisher

Oxford University Press (OUP)

Subject

Genetics

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