Kontis K J, Arfin S M
Department of Biological Chemistry, College of Medicine, University of California, Irvine 92717.
Mol Cell Biol. 1989 May;9(5):1832-8. doi: 10.1128/mcb.9.5.1832-1838.1989.
A cDNA for threonyl-tRNA synthetase was isolated from a human placental cDNA lambda gt11 expression library by immunological screening, and its identity was confirmed by hybrid-selected mRNA translation. With this cDNA used as a hybridization probe, borrelidin-resistant Chinese hamster ovary cells that overproduced threonyl-tRNA synthetase were shown to have increased levels of threonyl-tRNA synthetase mRNA and gene sequences. Amplification of the gene did not appear to have been accompanied by any major structural reorganizations.
通过免疫筛选从人胎盘cDNA λgt11表达文库中分离出苏氨酰-tRNA合成酶的cDNA,并通过杂交选择的mRNA翻译确认其身份。以该cDNA作为杂交探针,结果显示,过量产生苏氨酰-tRNA合成酶的抗硼relidin中国仓鼠卵巢细胞中,苏氨酰-tRNA合成酶mRNA和基因序列水平升高。该基因的扩增似乎并未伴随任何主要的结构重组。