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DDX3 depletion represses translation of mRNAs with complex 5' UTRs.
Calviello, Lorenzo; Venkataramanan, Srivats; Rogowski, Karol J; Wyler, Emanuel; Wilkins, Kevin; Tejura, Malvika; Thai, Bao; Krol, Jacek; Filipowicz, Witold; Landthaler, Markus; Floor, Stephen N.
Afiliação
  • Calviello L; Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Venkataramanan S; Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Rogowski KJ; Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, 13125 Berlin, Germany.
  • Wyler E; Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, 13125 Berlin, Germany.
  • Wilkins K; Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Tejura M; Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Thai B; Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Krol J; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
  • Filipowicz W; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Landthaler M; Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, 13125 Berlin, Germany.
  • Floor SN; IRI Life Sciences, Institut für Biologie, Humboldt Universität zu Berlin, Philippstraße 13, 10115 Berlin, Germany.
Nucleic Acids Res ; 49(9): 5336-5350, 2021 05 21.
Article em En | MEDLINE | ID: mdl-33905506
DDX3 is an RNA chaperone of the DEAD-box family that regulates translation. Ded1, the yeast ortholog of DDX3, is a global regulator of translation, whereas DDX3 is thought to preferentially affect a subset of mRNAs. However, the set of mRNAs that are regulated by DDX3 are unknown, along with the relationship between DDX3 binding and activity. Here, we use ribosome profiling, RNA-seq, and PAR-CLIP to define the set of mRNAs that are regulated by DDX3 in human cells. We find that while DDX3 binds highly expressed mRNAs, depletion of DDX3 particularly affects the translation of a small subset of the transcriptome. We further find that DDX3 binds a site on helix 16 of the human ribosomal rRNA, placing it immediately adjacent to the mRNA entry channel. Translation changes caused by depleting DDX3 levels or expressing an inactive point mutation are different, consistent with different association of these genetic variant types with disease. Taken together, this work defines the subset of the transcriptome that is responsive to DDX3 inhibition, with relevance for basic biology and disease states where DDX3 is altered.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article