| Literature DB >> 32926445 |
Ryota Kurimoto1, Tomoki Chiba1, Yoshiaki Ito1,2, Takahide Matsushima1, Yuki Yano1, Kohei Miyata3, Yuka Yashiro4, Tsutomu Suzuki5, Kozo Tomita4, Hiroshi Asahara1,6.
Abstract
Let-7 is an evolutionary conserved microRNA that mediates post-transcriptional gene silencing to regulate a wide range of biological processes, including development, differentiation, and tumor suppression. Let-7 biogenesis is tightly regulated by several RNA-binding proteins, including Lin28A/B, which represses let-7 maturation. To identify new regulators of let-7, we devised a cell-based functional screen of RNA-binding proteins using a let-7 sensor luciferase reporter and identified the tRNA pseudouridine synthase, TruB1. TruB1 enhanced maturation specifically of let-7 family members. Rather than inducing pseudouridylation of the miRNAs, high-throughput sequencing crosslinking immunoprecipitation (HITS-CLIP) and biochemical analyses revealed direct binding between endogenous TruB1 and the stem-loop structure of pri-let-7, which also binds Lin28A/B. TruB1 selectively enhanced the interaction between pri-let-7 and the microprocessor DGCR8, which mediates miRNA maturation. Finally, TruB1 suppressed cell proliferation, which was mediated in part by let-7. Altogether, we reveal an unexpected function for TruB1 in promoting let-7 maturation.Entities:
Keywords: RNA-binding protein; TruB1; let-7; microRNA; pseudouridine
Mesh:
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Year: 2020 PMID: 32926445 PMCID: PMC7560213 DOI: 10.15252/embj.2020104708
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598