Aminoacyl-tRNA synthetases: A new image for a classical family

被引:73
作者
Martinis, SA
Plateau, P
Cavarelli, J
Florentz, C
机构
[1] Inst Biol Mol & Cellulaire, CNRS, UPR 9002, F-67084 Strasbourg, France
[2] Univ Houston, Dept Biol & Biochem, Houston, TX 77204 USA
[3] Ecole Polytech, CNRS, UMR 7654, Biochim Lab, F-91128 Palaiseau, France
[4] Inst Genet Biol Mol & Cellulaire, Struct Biol Lab, F-67404 Illkirch Graffenstaden, France
基金
美国国家科学基金会;
关键词
aminoacyl-tRNA synthetases; molecular evolution; antibiotic; protein synthesis; RNA recognition; tRNA identity;
D O I
10.1016/S0300-9084(99)80126-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aminoacyl-tRNA synthetases (aaRSs) are a family of enzymes well known for their role in protein synthesis. More recent investigations have discovered that this classic family of enzymes is actually capable of a broad repertoire of functions which not only impact protein synthesis, but extend to a number of other critical cellular activities. Specific aaRSs play roles in cellular fidelity, tRNA processing, RNA splicing. RNA trafficking, apoptosis, transcriptional and translational regulation. A recent EMBO workshop entitled 'Structure and Function of Aminoacyl-tRNA Synthetases' (Mittelwihr, France, October 10-15, 1998), highlighted the diversity of the aaRSs 'role within the cell. These novel activities as well as significant advances in delineating mechanisms of substrate specificity and the aminoacylation reaction affirm the family of aaRSs as pharmaceutical targets. (C) 1999 Societe francaise de biochimie et biologie moleculaire / Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:683 / 700
页数:18
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