4.8 Article

Cryo-EM Structure of Human Dicer and Its Complexes with a Pre-miRNA Substrate

Journal

CELL
Volume 173, Issue 5, Pages 1191-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.03.080

Keywords

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Funding

  1. National Science Foundation of China [31530018, 31671355]
  2. National Key R&D Program of China [2016YFA0501100]
  3. Beijing Municipal Science & Technology Commission [Z161100000116034]

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Human Dicer (hDicer) is a multi-domain protein belonging to the RNase III family. It plays pivotal roles in small RNA biogenesis during the RNA interference (RNAi) pathway by processing a diverse range of double-stranded RNA (dsRNA) precursors to generate similar to 22 nt microRNA (miRNA) or small interfering RNA (siRNA) products for sequence-directed gene silencing. In this work, we solved the cryoelectron microscopy (cryo-EM) structure of hDicer in complex with its cofactor protein TRBP and revealed the precise spatial arrangement of hDicer's multiple domains. We further solved structures of the hDicer-TRBP complex bound with pre-let-7 RNA in two distinct conformations. In combination with biochemical analysis, these structures reveal a property of the hDicer-TRBP complex to promote the stability of pre-miRNA's stem duplex in a predicing state. These results provide insights into the mechanism of RNA processing by hDicer and illustrate the regulatory role of hDicer's N-terminal helicase domain.

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