Akimoto S, Ohnishi Y
Microbiol Immunol. 1982;26(9):779-93. doi: 10.1111/j.1348-0421.1982.tb00224.x.
The gene promoting nucleic-acid degradation (pnd) on IncIa plasmid R483 was cloned into pBR322. It is located on a 0.85 kilobase (kb) EcoRI-SalI fragment and is close to Tn7. The pnd gene has similar properties to the srnB gene on the F plasmid. A cleavage map of the 0.85 kb pnd fragment was constructed and compared with that of the 1.18 kb EcoRI-BamHI fragment containing the srnB gene. These two regions showed marked heterogeneity as evidenced by their distinctly different restriction maps. This result suggests separate paths of evolution of the two genes for stable RNA degradation.
将IncIa质粒R483上促进核酸降解的基因(pnd)克隆到pBR322中。它位于一个0.85千碱基(kb)的EcoRI - SalI片段上,且靠近Tn7。pnd基因具有与F质粒上的srnB基因相似的特性。构建了0.85 kb pnd片段的切割图谱,并与包含srnB基因的1.18 kb EcoRI - BamHI片段的图谱进行比较。这两个区域显示出明显的异质性,其限制酶切图谱明显不同就是证明。这一结果表明这两个稳定RNA降解基因的进化路径是分开的。