To kill a microRNA: emerging concepts in target-directed microRNA degradation

Author:

Buhagiar Amber F1ORCID,Kleaveland Benjamin1ORCID

Affiliation:

1. Department of Pathology and Lab Medicine , Weill Cornell Medicine, New York , NY 10065 , USA

Abstract

Abstract MicroRNAs (miRNAs) guide Argonaute (AGO) proteins to bind mRNA targets. Although most targets are destabilized by miRNA–AGO binding, some targets induce degradation of the miRNA instead. These special targets are also referred to as trigger RNAs. All triggers identified thus far have binding sites with greater complementarity to the miRNA than typical target sites. Target-directed miRNA degradation (TDMD) occurs when trigger RNAs bind the miRNA–AGO complex and recruit the ZSWIM8 E3 ubiquitin ligase, leading to AGO ubiquitination and proteolysis and subsequent miRNA destruction. More than 100 different miRNAs are regulated by ZSWIM8 in bilaterian animals, and hundreds of trigger RNAs have been predicted computationally. Disruption of individual trigger RNAs or ZSWIM8 has uncovered important developmental and physiologic roles for TDMD across a variety of model organisms and cell types. In this review, we highlight recent progress in understanding the mechanistic basis and functions of TDMD, describe common features of trigger RNAs, outline best practices for validating trigger RNAs, and discuss outstanding questions in the field.

Funder

National Institute of General Medical Sciences

Weill Cornell Medicine Department of Pathology and Lab Medicine Faculty

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference109 articles.

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