Title | To kill a microRNA: emerging concepts in target-directed microRNA degradation. |
Publication Type | Journal Article |
Year of Publication | 2024 |
Authors | Buhagiar AF, Kleaveland B |
Journal | Nucleic Acids Res |
Volume | 52 |
Issue | 4 |
Pagination | 1558-1574 |
Date Published | 2024 Feb 28 |
ISSN | 1362-4962 |
Keywords | Animals, Argonaute Proteins, Binding Sites, MicroRNAs, Proteolysis, RNA Stability, Ubiquitination |
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. |
DOI | 10.1093/nar/gkae003 |
Alternate Journal | Nucleic Acids Res |
PubMed ID | 38224449 |
PubMed Central ID | PMC10899785 |
Grant List | R35 GM147463 / GM / NIGMS NIH HHS / United States R35GM147463 / GM / NIGMS NIH HHS / United States |
Related Lab:
Related Faculty:
Benjamin Kleaveland, M.D., Ph.D.