Hypoxia and regulation of messenger RNA translation
- PMID: 17998058
- DOI: 10.1016/S0076-6879(07)35013-1
Hypoxia and regulation of messenger RNA translation
Abstract
Poor oxygenation (hypoxia) influences important physiological and pathological conditions, including development, ischemia, stroke, and cancer. The influence of hypoxia is due in large part to changes in gene expression, which occur through changes in transcription and translation. In response to hypoxic conditions, cells reduce their overall rate of messenger RNA (mRNA) translation. However, individual mRNA species are effected to highly varying degrees, with some even translationally stimulated under these conditions. Regulation of translation in response to hypoxia thereby gives rise to differential gene expression. The ability of cells to regulate translation during hypoxia is important for their survival. In the first part of this chapter, we review the effects of hypoxia on overall and gene-specific mRNA translation efficiencies and summarize the molecular pathways activated by hypoxia that regulate mRNA translation. In the second part, we describe the methods employed to investigate overall and gene-specific translation, including radioactive metabolic labeling, polysome fractionation, and reporter assays. We have emphasized the qualitative and quantitative analysis of polysome profiles, which can yield interesting information regarding the mechanistic basis for (gene-specific) translational regulation.
Similar articles
-
Phosphorylation of eIF2alpha is required for mRNA translation inhibition and survival during moderate hypoxia.Radiother Oncol. 2007 Jun;83(3):353-61. doi: 10.1016/j.radonc.2007.04.031. Epub 2007 May 24. Radiother Oncol. 2007. PMID: 17531337
-
Cellular oxygen sensing, signalling and how to survive translational arrest in hypoxia.Acta Physiol (Oxf). 2009 Feb;195(2):205-30. doi: 10.1111/j.1748-1716.2008.01894.x. Epub 2008 Sep 1. Acta Physiol (Oxf). 2009. PMID: 18764866 Review.
-
Selective mRNA translation coordinates energetic and metabolic adjustments to cellular oxygen deprivation and reoxygenation in Arabidopsis thaliana.Plant J. 2008 Dec;56(5):743-55. doi: 10.1111/j.1365-313X.2008.03642.x. Epub 2008 Aug 23. Plant J. 2008. PMID: 18665916
-
Oxygen-dependent regulation of NDRG1 in human glioblastoma cells in vitro and in vivo.Oncol Rep. 2009 Jan;21(1):237-46. Oncol Rep. 2009. PMID: 19082468
-
"Translating" tumor hypoxia: unfolded protein response (UPR)-dependent and UPR-independent pathways.Mol Cancer Res. 2006 Jul;4(7):423-36. doi: 10.1158/1541-7786.MCR-06-0150. Mol Cancer Res. 2006. PMID: 16849518 Review.
Cited by
-
Hypoxia-induced alteration of mitochondrial genes in cardiomyocytes: role of Bnip3 and Pdk1.Shock. 2010 Aug;34(2):169-75. doi: 10.1097/SHK.0b013e3181cffe7d. Shock. 2010. PMID: 20160671 Free PMC article.
-
Systematic identification of gene activities promoting hypoxic death.Genetics. 2009 Feb;181(2):483-96. doi: 10.1534/genetics.108.097188. Epub 2008 Dec 1. Genetics. 2009. PMID: 19047414 Free PMC article.
-
Functional importance of Dicer protein in the adaptive cellular response to hypoxia.J Biol Chem. 2012 Aug 17;287(34):29003-20. doi: 10.1074/jbc.M112.373365. Epub 2012 Jun 28. J Biol Chem. 2012. PMID: 22745131 Free PMC article.
-
Genome-wide identification and annotation of HIF-1α binding sites in two cell lines using massively parallel sequencing.Hugo J. 2010 Dec;4(1-4):35-48. doi: 10.1007/s11568-011-9150-9. Epub 2011 Feb 19. Hugo J. 2010. PMID: 22132063 Free PMC article.
-
Analysis of translation initiation during stress conditions by polysome profiling.J Vis Exp. 2014 May 19;(87):51164. doi: 10.3791/51164. J Vis Exp. 2014. PMID: 24893838 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources