Translation matters: protein synthesis defects in inherited disease - PubMed
Review
Translation matters: protein synthesis defects in inherited disease
Gert C Scheper et al. Nat Rev Genet. 2007 Sep.
Abstract
The list of genetic diseases caused by mutations that affect mRNA translation is rapidly growing. Although protein synthesis is a fundamental process in all cells, the disease phenotypes show a surprising degree of heterogeneity. Studies of some of these diseases have provided intriguing new insights into the functions of proteins involved in the process of translation; for example, evidence suggests that several have other functions in addition to their roles in translation. Given the numerous proteins involved in mRNA translation, it is likely that further inherited diseases will turn out to be caused by mutations in genes that are involved in this complex process.
Similar articles
-
Mutational analysis of the ribosome.
Triman KL. Triman KL. Adv Genet. 2007;58:89-119. doi: 10.1016/S0065-2660(06)58004-6. Adv Genet. 2007. PMID: 17452247 Review.
-
[Translation termination factors and prions].
Nakamura Y. Nakamura Y. Tanpakushitsu Kakusan Koso. 2006 Dec;51(16 Suppl):2574-82. Tanpakushitsu Kakusan Koso. 2006. PMID: 17471981 Review. Japanese. No abstract available.
-
Starting the protein synthesis machine: eukaryotic translation initiation.
Preiss T, W Hentze M. Preiss T, et al. Bioessays. 2003 Dec;25(12):1201-11. doi: 10.1002/bies.10362. Bioessays. 2003. PMID: 14635255 Review.
-
Mie M, Shimizu S, Takahashi F, Kobatake E. Mie M, et al. Biochem Biophys Res Commun. 2008 Aug 15;373(1):48-52. doi: 10.1016/j.bbrc.2008.05.173. Epub 2008 Jun 9. Biochem Biophys Res Commun. 2008. PMID: 18544339
-
Recent mechanistic insights into eukaryotic ribosomes.
Rodnina MV, Wintermeyer W. Rodnina MV, et al. Curr Opin Cell Biol. 2009 Jun;21(3):435-43. doi: 10.1016/j.ceb.2009.01.023. Epub 2009 Feb 23. Curr Opin Cell Biol. 2009. PMID: 19243929 Review.
Cited by
-
Current Status and Future Opportunities of Omics Tools in Mycotoxin Research.
Eshelli M, Qader MM, Jambi EJ, Hursthouse AS, Rateb ME. Eshelli M, et al. Toxins (Basel). 2018 Oct 26;10(11):433. doi: 10.3390/toxins10110433. Toxins (Basel). 2018. PMID: 30373184 Free PMC article. Review.
-
Nogales-Gadea G, Mormeneo E, García-Consuegra I, Rubio JC, Orozco A, Arenas J, Martín MA, Lucia A, Gómez-Foix AM, Martí R, Andreu AL. Nogales-Gadea G, et al. PLoS One. 2010 Oct 5;5(10):e13164. doi: 10.1371/journal.pone.0013164. PLoS One. 2010. PMID: 20957198 Free PMC article.
-
Vanishing white matter: a leukodystrophy due to astrocytic dysfunction.
Bugiani M, Vuong C, Breur M, van der Knaap MS. Bugiani M, et al. Brain Pathol. 2018 May;28(3):408-421. doi: 10.1111/bpa.12606. Brain Pathol. 2018. PMID: 29740943 Free PMC article. Review.
-
Ma T. Ma T. J Neurochem. 2023 Jul;166(1):47-57. doi: 10.1111/jnc.15541. Epub 2021 Nov 27. J Neurochem. 2023. PMID: 34796967 Free PMC article. Review.
-
Hashimoto K, Ishima T. Hashimoto K, et al. PLoS One. 2010 Nov 8;5(11):e15430. doi: 10.1371/journal.pone.0015430. PLoS One. 2010. PMID: 21151481 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical