Literature DB >> 32220646

Cryo-EM Structures of Human Drosha and DGCR8 in Complex with Primary MicroRNA.

Alexander C Partin1, Kaiming Zhang2, Byung-Cheon Jeong1, Emily Herrell1, Shanshan Li2, Wah Chiu3, Yunsun Nam4.   

Abstract

Metazoan microRNAs require specific maturation steps initiated by Microprocessor, comprising Drosha and DGCR8. Lack of structural information for the assembled complex has hindered an understanding of how Microprocessor recognizes primary microRNA transcripts (pri-miRNAs). Here we present a cryoelectron microscopy structure of human Microprocessor with a pri-miRNA docked in the active site, poised for cleavage. The basal junction is recognized by a four-way intramolecular junction in Drosha, triggered by the Belt and Wedge regions that clamp over the ssRNA. The belt is important for efficiency and accuracy of pri-miRNA processing. Two dsRBDs form a molecular ruler to measure the stem length between the two dsRNA-ssRNA junctions. The specific organization of the dsRBDs near the apical junction is independent of Drosha core domains, as observed in a second structure in the partially docked state. Collectively, we derive a molecular model to explain how Microprocessor recognizes a pri-miRNA and accurately identifies the cleavage site.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  DGCR8; Drosha; Microprocessor; RNA processing; RNase III; cryo-EM; dsRBD; microRNA; pri-miRNA; structure

Mesh:

Substances:

Year:  2020        PMID: 32220646      PMCID: PMC7214211          DOI: 10.1016/j.molcel.2020.02.016

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


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