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Modulation of RNA Condensation by the DEAD-Box Protein eIF4A.
Tauber, Devin; Tauber, Gabriel; Khong, Anthony; Van Treeck, Briana; Pelletier, Jerry; Parker, Roy.
Afiliación
  • Tauber D; Department of Biochemistry, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Tauber G; Department of Biochemistry, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Khong A; Department of Biochemistry, University of Colorado Boulder, Boulder, CO 80309, USA; Howard Hughes Medical Institute, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Van Treeck B; Department of Biochemistry, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Pelletier J; Department of Biochemistry, McGill University, Montreal, QC H3G 1Y6, Canada; The Rosalind and Morris Goodman Cancer Research Center and the Department of Oncology, McGill University, Montreal, QC, Canada.
  • Parker R; Department of Biochemistry, University of Colorado Boulder, Boulder, CO 80309, USA; Howard Hughes Medical Institute, University of Colorado Boulder, Boulder, CO 80309, USA. Electronic address: roy.parker@colorado.edu.
Cell ; 180(3): 411-426.e16, 2020 02 06.
Article en En | MEDLINE | ID: mdl-31928844
Stress granules are condensates of non-translating mRNAs and proteins involved in the stress response and neurodegenerative diseases. Stress granules form in part through intermolecular RNA-RNA interactions, and to better understand how RNA-based condensation occurs, we demonstrate that RNA is effectively recruited to the surfaces of RNA or RNP condensates in vitro. We demonstrate that, through ATP-dependent RNA binding, the DEAD-box protein eIF4A reduces RNA condensation in vitro and limits stress granule formation in cells. This defines a function for eIF4A to limit intermolecular RNA-RNA interactions in cells. These results establish an important role for eIF4A, and potentially other DEAD-box proteins, as ATP-dependent RNA chaperones that limit the condensation of RNA, analogous to the function of proteins like HSP70 in combatting protein aggregates.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ribonucleoproteínas / Saccharomyces cerevisiae / ARN de Hongos / ARN Helicasas / Proteínas de Saccharomyces cerevisiae / Factor 4A Eucariótico de Iniciación / Factor 4F Eucariótico de Iniciación / ARN Helicasas DEAD-box Límite: Humans Idioma: En Revista: Cell Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ribonucleoproteínas / Saccharomyces cerevisiae / ARN de Hongos / ARN Helicasas / Proteínas de Saccharomyces cerevisiae / Factor 4A Eucariótico de Iniciación / Factor 4F Eucariótico de Iniciación / ARN Helicasas DEAD-box Límite: Humans Idioma: En Revista: Cell Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos