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从耐辐射球菌中克隆DNA修复基因mtcA、mtcB、uvsC、uvsD、uvsE以及亮氨酸基因leuB。

Cloning of the DNA repair genes mtcA, mtcB, uvsC, uvsD, uvsE and the leuB gene from Deinococcus radiodurans.

作者信息

Al-Bakri G H, Mackay M W, Whittaker P A, Moseley B E

出版信息

Gene. 1985;33(3):305-11. doi: 10.1016/0378-1119(85)90238-0.

Abstract

A gene library from Deinococcus radiodurans has been constructed in the cosmid pJBFH. A 51.5-kb hybrid cosmid, pUE40, that transduced Escherichia coli HB101 from leucine dependence to independence was selected, and a 6.9-kb fragment which carried the leuB gene from D. radiodurans was subcloned into the EcoRI site of pAT153. The DNA repair genes mtcA, mtcB, uvsC, uvsD and uvsE, which code for two D. radiodurans UV endonucleases were identified by transforming appropriate repair-deficient mutants of D. radiodurans to repair proficiency with DNA derived from the gene library. Hybrid cosmid pUE50 (37.9 kb) containing an insert carrying both the mtcA and mtcB genes was selected and 5.6- and 2.7-kb DNA fragments carrying mtcA and mtcB, respectively, i.e., the genes that code for UV endonuclease alpha, were subcloned into the EcoRI site of pAT153. The three genes uvsC, uvsD and uvsE, that code for UV endonuclease beta, were all present in the 46.0-kb hybrid cosmid pUE60. The uvsE gene in a 12.2-kb fragment was subcloned into the HindIII site of pAT153 and the size of the insert reduced to 6.1 kb by deletion of a 6.7-kb fragment from the hybrid plasmid pUE62. None of the uvs genes introduced into the UV-sensitive E. coli CSR603 (uvrA-) was able to complement its repair defect. The mtcA, uvsC, uvsD and uvsE genes were found in the 52.5-kb hybrid cosmid pUE70. It is concluded that the DNA repair genes mtcA, mtcB, uvsC, uvsD and uvsE are located within an 83.0-kb fragment of the D. radiodurans genome.

摘要

已在粘粒pJBFH中构建了来自耐辐射球菌的基因文库。筛选出一个51.5 kb的杂种粘粒pUE40,它能将大肠杆菌HB101从亮氨酸依赖型转化为非依赖型,并且将一个携带耐辐射球菌leuB基因的6.9 kb片段亚克隆到pAT153的EcoRI位点。通过用来自基因文库的DNA将耐辐射球菌合适的修复缺陷型突变体转化为修复 proficient 型,鉴定出了编码两种耐辐射球菌紫外线内切核酸酶的DNA修复基因mtcA、mtcB、uvsC、uvsD和uvsE。选择了含有携带mtcA和mtcB基因的插入片段的杂种粘粒pUE50(37.9 kb),并将分别携带mtcA和mtcB的5.6 kb和2.7 kb DNA片段,即编码紫外线内切核酸酶α的基因,亚克隆到pAT153的EcoRI位点。编码紫外线内切核酸酶β的三个基因uvsC、uvsD和uvsE都存在于46.0 kb的杂种粘粒pUE60中。将一个12.2 kb片段中的uvsE基因亚克隆到pAT153的HindIII位点,并通过从杂种质粒pUE62中缺失一个6.7 kb片段将插入片段大小减小到6.1 kb。导入对紫外线敏感的大肠杆菌CSR603(uvrA-)的任何uvs基因都不能弥补其修复缺陷。在52.5 kb的杂种粘粒pUE70中发现了mtcA、uvsC、uvsD和uvsE基因。得出结论,DNA修复基因mtcA、mtcB、uvsC、uvsD和uvsE位于耐辐射球菌基因组的一个83.0 kb片段内。

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