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PMID: 17680008 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Translation matters: protein synthesis defects in inherited disease.

Nature reviews. Genetics ·Vol. 8 ·No. 9 ·2007-09-00 ·Pages 711-23

Scheper GC, van der Knaap MS, Proud CG

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.

MeSH Terms
5' Untranslated Regions/genetics Animals Gene Expression Regulation Genetic Diseases, Inborn/genetics,metabolism Humans Mitochondria/genetics Models, Biological Mutation/physiology Peptide Elongation Factors/genetics Peptide Initiation Factors/genetics Peptide Termination Factors/genetics Protein Biosynthesis/genetics RNA, Transfer/genetics Ribosomes/genetics
Chemicals
5' Untranslated Regions Peptide Elongation Factors Peptide Initiation Factors Peptide Termination Factors RNA, Transfer
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Scheper Gert C
Department of Child Neurology/Center for Neurogenomics and Cognitive Research, Vrije Universiteit Medical Center, De Boelelaan 1117, 1081HV Amsterdam, The Netherlands.
van der Knaap Marjo S
Proud Christopher G
Article Info
Journal
Nature reviews. Genetics
Abbr.
Nat Rev Genet
ISSN
1471-0056
Published
2007-09-00
Epub
2007-00-31
Pages
711-23
Language
English
Region
England
NLM ID
100962779
Subset
IM
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