Aujame L, Yatscoff R W, Freeman K B
Can J Biochem. 1978 Jun;56(6):592-7. doi: 10.1139/o78-089.
The possible existence of mammalian mitochondrial asparaginyl-tRNA has been examined using a variety of approaches. [3H]Asparagine was incorporated into protein by mitochondria of the Chinese hamster ovary (CHO) cell line Asn-7, which has a temperature-sensitive cytosolic asparaginyl-tRNA synthetase, either in the presence of cycloheximide or at a nonpermissive temperature. Isolated mitochondria of CHO thymidine kinase minus (TK-) cells also incorporated the amino acid into protein. In each case, the number and electrophoretic mobility of the proteins was the same as mitochondrially synthesized proteins of CHO TK- cells labelled with [35S]methionine. A tRNAAsn could be charged in isolated CHO TK- cell mitochondria and the asparaginyl-tRNA was found to elute before its cytosolic counterpart on an RPC-5 column and to have a higher mobility on polyacrylamide slab gels run under denaturing conditions. This is the first demonstration of a unique mitochondrial asparaginyl-tRNA.
已使用多种方法研究了哺乳动物线粒体天冬酰胺基 - tRNA可能的存在情况。[3H]天冬酰胺在环己酰亚胺存在下或在非允许温度下,被中国仓鼠卵巢(CHO)细胞系Asn - 7的线粒体掺入蛋白质中,该细胞系具有温度敏感的胞质天冬酰胺基 - tRNA合成酶。CHO胸苷激酶缺陷(TK -)细胞的分离线粒体也将该氨基酸掺入蛋白质中。在每种情况下,蛋白质的数量和电泳迁移率与用[35S]甲硫氨酸标记的CHO TK -细胞的线粒体合成蛋白质相同。在分离的CHO TK -细胞线粒体中,tRNAAsn可以被充电,并且发现天冬酰胺基 - tRNA在RPC - 5柱上比其胞质对应物先洗脱,并且在变性条件下运行的聚丙烯酰胺平板凝胶上具有更高的迁移率。这是独特的线粒体天冬酰胺基 - tRNA的首次证明。