Translation matters: protein synthesis defects in inherited disease
- PMID: 17680008
- DOI: 10.1038/nrg2142
Translation matters: protein synthesis defects in inherited disease
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.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].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.Bioessays. 2003 Dec;25(12):1201-11. doi: 10.1002/bies.10362. Bioessays. 2003. PMID: 14635255 Review.
-
Selection of mRNA 5'-untranslated region sequence with high translation efficiency through ribosome display.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.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
-
Translation initiation requires cell division cycle 123 (Cdc123) to facilitate biogenesis of the eukaryotic initiation factor 2 (eIF2).J Biol Chem. 2013 Jul 26;288(30):21537-46. doi: 10.1074/jbc.M113.472290. Epub 2013 Jun 17. J Biol Chem. 2013. PMID: 23775072 Free PMC article.
-
Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study.Eur J Hum Genet. 2009 Aug;17(8):1056-62. doi: 10.1038/ejhg.2009.4. Epub 2009 Feb 11. Eur J Hum Genet. 2009. PMID: 19209188 Free PMC article.
-
Binding of eIF3 in complex with eIF5 and eIF1 to the 40S ribosomal subunit is accompanied by dramatic structural changes.Nucleic Acids Res. 2019 Sep 5;47(15):8282-8300. doi: 10.1093/nar/gkz570. Nucleic Acids Res. 2019. PMID: 31291455 Free PMC article.
-
IGHMBP2 deletion suppresses translation and activates the integrated stress response.Life Sci Alliance. 2024 May 21;7(8):e202302554. doi: 10.26508/lsa.202302554. Print 2024 Aug. Life Sci Alliance. 2024. PMID: 38803225 Free PMC article.
-
The effect of mutated mitochondrial ribosomal proteins S16 and S22 on the assembly of the small and large ribosomal subunits in human mitochondria.Mitochondrion. 2008 Jun;8(3):254-61. doi: 10.1016/j.mito.2008.04.004. Epub 2008 Apr 30. Mitochondrion. 2008. PMID: 18539099 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical