The ZSWIM8 ubiquitin ligase mediates target-directed microRNA degradation

Author:

Shi Charlie Y.123ORCID,Kingston Elena R.123ORCID,Kleaveland Benjamin4ORCID,Lin Daniel H.123ORCID,Stubna Michael W.123ORCID,Bartel David P.123ORCID

Affiliation:

1. Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

2. Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

3. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

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

Abstract

Turning the tables on microRNA decay MicroRNAs help to regulate many genes in animal cells. Each microRNA associates with an Argonaute (AGO) protein, forming a complex in which the microRNA pairs with a messenger RNA (mRNA) target and AGO recruits factors that accelerate mRNA decay. However, for some unusual targets, the reverse occurs: Pairing to the target recruits factors that accelerate microRNA decay rather than degradation of the mRNA. Working independently, Shi et al. and Han et al. elucidate the mechanism of this phenomenon. They found that pairing to the unusual targets recruits a ubiquitin ligase that causes degradation of AGO, thereby exposing the microRNA to cellular nucleases. Mutating the ubiquitin ligase in diverse animals and cell types deregulates numerous microRNAs, implying that this phenomenon is widely deployed to sculpt microRNA levels. Science , this issue p. eabc9359 , p. eabc9546

Funder

National Science Foundation

National Institutes of Health

Howard Hughes Medical Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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