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Cryo-EM Structures of Human Drosha and DGCR8 in Complex with Primary MicroRNA.
Partin, Alexander C; Zhang, Kaiming; Jeong, Byung-Cheon; Herrell, Emily; Li, Shanshan; Chiu, Wah; Nam, Yunsun.
Afiliación
  • Partin AC; Laboratory of RNA Biology, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Departments of Biophysics and Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Zhang K; Department of Bioengineering and James H. Clark Center, Stanford University, Stanford, CA 94305, USA.
  • Jeong BC; Laboratory of RNA Biology, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Departments of Biophysics and Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Herrell E; Laboratory of RNA Biology, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Departments of Biophysics and Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Li S; Department of Bioengineering and James H. Clark Center, Stanford University, Stanford, CA 94305, USA.
  • Chiu W; Department of Bioengineering and James H. Clark Center, Stanford University, Stanford, CA 94305, USA; CryoEM and Bioimaging Division, SSRL, SLAC National Accelerator Laboratory, Stanford University, Menlo Park, CA 94025, USA.
  • Nam Y; Laboratory of RNA Biology, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Departments of Biophysics and Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electro
Mol Cell ; 78(3): 411-422.e4, 2020 05 07.
Article en En | MEDLINE | ID: mdl-32220646
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al ARN / MicroARNs / Ribonucleasa III Límite: Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al ARN / MicroARNs / Ribonucleasa III Límite: Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos