Weygand-Durasević I, Nalaskowska M, Söll D
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511.
J Bacteriol. 1994 Jan;176(1):232-9. doi: 10.1128/jb.176.1.232-239.1994.
In order to gain insight into the conservation of determinants for tRNA identity between organisms, Schizosaccharomyces pombe and human amber suppressor serine tRNA genes have been examined for functional expression in Escherichia coli. The primary transcripts, which originated from E. coli plasmid promoters, were processed into mature tRNAs, but they were poorly aminoacylated in E. coli and thus were nonfunctional as suppressors in vivo. However, coexpression of cloned Saccharomyces cerevisiae seryl-tRNA synthetase led to efficient suppression in E. coli. This shows that some, but not all, determinants specifying the tRNASer identity are conserved in evolution.
为了深入了解不同生物体之间tRNA身份决定因素的保守性,对粟酒裂殖酵母和人类琥珀抑制型丝氨酸tRNA基因在大肠杆菌中的功能表达进行了研究。源自大肠杆菌质粒启动子的初级转录本被加工成成熟的tRNA,但它们在大肠杆菌中氨基酰化程度很低,因此在体内作为抑制子无功能。然而,克隆的酿酒酵母丝氨酰-tRNA合成酶的共表达导致在大肠杆菌中有效抑制。这表明,在进化过程中,一些(但不是全部)决定tRNASer身份的决定因素是保守的。