Maruyama I N, Horikoshi K, Nagase Y, Soma M, Nobuhara M, Yasuda S, Hirota Y
National Institute of Genetics, Mishima, Japan.
Gene Anal Tech. 1989 May-Jun;6(3):57-61. doi: 10.1016/0735-0651(89)90011-3.
A 41-nucleotide-long duplex DNA, which contains the translation termination codon TAA in six reading frames and lactose operator sequence of Escherichia coli, has been synthesized. This fragment may be useful not only for producing a truncated protein encoded in a plasmid, but also for the identification of the precise coding region and translation direction of a bacterial gene in the cloned chromosomal segment. The synthetic fragment was inserted into beta-lactamase structural gene in pBR322 in order to test the in vivo activity. The plasmid produced mutant beta-lactamase reduced in size, as expected from the insertion site, and rendered the host bacterium constitutive for beta-galactosidase. Thus, termination codons and lactose operator in synthetic nucleotide appear to be functional in vivo.
已合成一段41个核苷酸长的双链DNA,它在六个阅读框中包含翻译终止密码子TAA以及大肠杆菌的乳糖操纵序列。该片段不仅可用于产生质粒中编码的截短蛋白,还可用于鉴定克隆染色体片段中细菌基因的精确编码区和翻译方向。将合成片段插入pBR322中的β-内酰胺酶结构基因,以测试其体内活性。正如从插入位点所预期的那样,该质粒产生了大小减小的突变型β-内酰胺酶,并使宿主细菌对β-半乳糖苷酶呈组成型表达。因此,合成核苷酸中的终止密码子和乳糖操纵序列在体内似乎具有功能。