Literature DB >> 10557103

Regulation of translation initiation following stress.

M S Sheikh1, A J Fornace.   

Abstract

Recent studies suggest that genotoxic and non-genotoxic stresses appear to invoke translational checkpoints in order to inhibit protein synthesis. Depending on the stress and/or cell type, this downregulation of protein synthesis may either (i) protect against the deleterious effects of noxious agents and ensure the conservation of resources that are needed to survive under adverse conditions or (ii) activate apoptosis. In this article, we have reviewed several lines of evidence which support the notion that regulation of translation initiation is an important component of the cellular stress response. While the stress-induced post-translational regulation of translation initiation factors (eIFs) has been well documented, stress-induced regulation of eIFs at the mRNA levels, as reviewed here, is only beginning to be elucidated. Thus, the stress-mediated regulation of eIFs occurs at multiple different levels involving, transcriptional, post-transcriptional and post-translational controls.

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Year:  1999        PMID: 10557103     DOI: 10.1038/sj.onc.1203131

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  41 in total

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4.  Inhibition of hepatitis B virus replication by cIAP2 involves accelerating the ubiquitin-proteasome-mediated destruction of polymerase.

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5.  Engineering ribosomal leaky scanning and upstream open reading frames for precise control of protein translation.

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7.  Simultaneous gene expression analysis of steady-state and actively translated mRNA populations from osteosarcoma MG-63 cells in response to IL-1alpha via an open expression analysis platform.

Authors:  Jingfang Ju; Chunli Huang; Stacey A Minskoff; Jane E Mayotte; Bruce E Taillon; Jan F Simons
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

8.  Translational control analysis by translationally active RNA capture/microarray analysis (TrIP-Chip).

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9.  Molecular mechanism of chemoresistance by miR-215 in osteosarcoma and colon cancer cells.

Authors:  Bo Song; Yuan Wang; Matthew A Titmus; Galina Botchkina; Andrea Formentini; Marko Kornmann; Jingfang Ju
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10.  Translation of TRAF1 is regulated by IRES-dependent mechanism and stimulated by vincristine.

Authors:  Lin Yang; Lubing Gu; Zhuoya Li; Muxiang Zhou
Journal:  Nucleic Acids Res       Date:  2010-04-22       Impact factor: 16.971

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