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A Mechanism for microRNA Arm Switching Regulated by Uridylation

Cited 41 time in Web of Science Cited 45 time in Scopus
Authors

Kim, Haedong; Kim, Jimi; Yu, Sha; Lee, Young-Yoon; Park, Junseong; Choi, Ran Joo; Yoon, Seon-Jin; Kang, Seok-Gu; Kim, V. Narry

Issue Date
2020-06
Publisher
Cell Press
Citation
Molecular Cell, Vol.78 No.6, pp.1224-1236.e5
Abstract
Strand selection is a critical step in microRNA (miRNA) biogenesis. Although the dominant strand may change depending on cellular contexts, the molecular mechanism and physiological significance of such alternative strand selection (or "arm switching") remain elusive. Here we find miR-324 to be one of the strongly regulated miRNAs by arm switching and identify the terminal uridylyl transferases TUT4 and TUT7 to be the key regulators. Uridylation of pre-miR-324 by TUT4/7 re-positions DICER on the pre-miRNA and shifts the cleavage site. This alternative processing produces a duplex with a different terminus from which the 3' strand (3p) is selected instead of the 5' strand (5p). In glioblastoma, the TUT4/7 and 3p levels are upregulated, whereas the 5p level is reduced. Manipulation of the strand ratio is sufficient to impair glioblastoma cell proliferation. This study uncovers a role of uridylation as a molecular switch in alternative strand selection and implicates its therapeutic potential.
ISSN
1097-2765
URI
https://hdl.handle.net/10371/171900
DOI
https://doi.org/10.1016/j.molcel.2020.04.030
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

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