Kanaya S, Crouch R J
J Bacteriol. 1983 May;154(2):1021-6. doi: 10.1128/jb.154.2.1021-1026.1983.
The DNA coding for RNase H from a mutant strain of Escherichia coli (FB2) was cloned into plasmid pBR322. DNA sequence analysis and the exchange of a portion of the mutant and wild-type genes revealed that a single-base alteration (C-->T) in the coding region of the structural gene for RNase H is responsible for the difference in RNase H activity of the wild-type and mutant cells.
将来自大肠杆菌突变菌株(FB2)的核糖核酸酶H的DNA编码克隆到质粒pBR322中。DNA序列分析以及突变型和野生型基因部分的交换表明,核糖核酸酶H结构基因编码区的单碱基改变(C→T)导致了野生型和突变型细胞核糖核酸酶H活性的差异。