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RBM33 directs the nuclear export of transcripts containing GC-rich elements.
Thomas, Anu; Rehfeld, Frederick; Zhang, He; Chang, Tsung-Cheng; Goodarzi, Mohammad; Gillet, Frank; Mendell, Joshua T.
Afiliación
  • Thomas A; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Rehfeld F; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Zhang H; Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Chang TC; Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Goodarzi M; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Gillet F; Department of Immunology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
  • Mendell JT; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Genes Dev ; 36(9-10): 550-565, 2022 05 01.
Article en En | MEDLINE | ID: mdl-35589130
ABSTRACT
Although splicing is a major driver of RNA nuclear export, many intronless RNAs are efficiently exported to the cytoplasm through poorly characterized mechanisms. For example, GC-rich sequences promote nuclear export in a splicing-independent manner, but how GC content is recognized and coupled to nuclear export is unknown. Here, we developed a genome-wide screening strategy to investigate the mechanism of export of NORAD, an intronless cytoplasmic long noncoding RNA (lncRNA). This screen revealed an RNA binding protein, RBM33, that directs the nuclear export of NORAD and numerous other transcripts. RBM33 directly binds substrate transcripts and recruits components of the TREX-NXF1/NXT1 RNA export pathway. Interestingly, high GC content emerged as the feature that specifies RBM33-dependent nuclear export. Accordingly, RBM33 directly binds GC-rich elements in target transcripts. These results provide a broadly applicable strategy for the genetic dissection of nuclear export mechanisms and reveal a long-sought nuclear export pathway for transcripts with GC-rich sequences.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN Viral / Proteínas de Transporte Nucleocitoplasmático Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN Viral / Proteínas de Transporte Nucleocitoplasmático Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos