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New means to an end: mRNA export activity impacts alternative polyadenylation.
Shin, Jihae; Cheng, Hong; Tian, Bin.
Afiliación
  • Shin J; Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, NJ, USA.
  • Cheng H; State Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, China.
  • Tian B; Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, NJ, USA.
Transcription ; 10(4-5): 207-211, 2019.
Article en En | MEDLINE | ID: mdl-31474181
ABSTRACT
Gene expression involves multiple co- and post-transcriptional processes that have been increasingly found intertwined. A recent work by our groups (Chen et al. Mol Cell, 2019) indicates that expression of alternative polyadenylation isoforms in mammalian cells can be controlled by nuclear export activities. This regulation has distinct impacts on genes having different sizes and nucleotide contents, and involves RNA polymerase II distribution toward the 3' end of genes. This work raises a number of intriguing questions concerning how 3' end processing and nuclear export are integrated and how their regulation feeds back to transcription.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN Polimerasa II / ARN Mensajero / Núcleo Celular Límite: Animals / Humans Idioma: En Revista: Transcription Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN Polimerasa II / ARN Mensajero / Núcleo Celular Límite: Animals / Humans Idioma: En Revista: Transcription Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
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