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Radiation-induced translational control of gene expression.
Wahba, Amy; Lehman, Stacey L; Tofilon, Philip J.
Afiliación
  • Wahba A; Radiation Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Lehman SL; Radiation Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Tofilon PJ; Radiation Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
Translation (Austin) ; 5(1): e1265703, 2017.
Article en En | MEDLINE | ID: mdl-28702276
ABSTRACT
Radiation-induced gene expression has long been hypothesized to protect against cell death. Defining this process would provide not only insight into the mechanisms mediating cell survival after radiation exposure, but also a novel source of targets for radiosensitization. However, whereas the radiation-induced gene expression profiles using total cellular mRNA have been generated for cell lines as well as normal tissues, with few exception, the changes in mRNA do not correlate with changes in the corresponding protein. The traditional approach to profiling gene expression, i.e., using total cellular RNA, does not take into account posttranscriptional regulation. In this review, we describe the use of gene expression profiling of polysome-bound RNA to establish that radiation modifies gene expression via translational control. Because changes in polysome-bound mRNA correlate with changes in protein, analysis of the translational profiles provides a unique data set for investigating the mechanisms mediating cellular radioresponse.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Translation (Austin) Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Translation (Austin) Año: 2017 Tipo del documento: Article