van de Putte P, Plasterk R, Kuijpers A
J Bacteriol. 1984 May;158(2):517-22. doi: 10.1128/jb.158.2.517-522.1984.
The Gin product catalyzes an inversion of 3,000 base pairs of DNA in the genome of bacteriophage Mu. The orientation of the invertible of G-region determines the host range of the phage. Gin- mutants are complemented by a host function in strain HB101 and several other Escherichia coli K-12 strains. At least three clones in the E. coli gene bank described previously (L. Clarke and J. Carbon, Cell 9:91-99, 1976) contained the gin complementing function. This function, which we named pin, catalyzes an inversion of 1,800 base pairs in the adjacent DNA. The invertible region, named the P-region, together with pin, was further subcloned on pBR322. Conjugation and transduction experiments mapped the pin gene between the genes purB and fabD near position 25 on the E. coli chromosome. Also situated in this region is e14, a cryptic, UV- excisable , genetic element (A. Greener and C.W. Hill, J. Bacteriol . 144:312-321, 1980). We demonstrated that pin and the P-region are part of e 14. The e 14 element was cloned on pBR322 by genetic manipulation techniques in vivo. It has the properties of a defective prophage containing integration and excision functions and a SOS-sensitive repressor.
Gin产物催化噬菌体Mu基因组中3000个碱基对的DNA倒位。G区可倒位片段的方向决定了噬菌体的宿主范围。Gin突变体在HB101菌株和其他几种大肠杆菌K - 12菌株中可由宿主功能互补。先前描述的大肠杆菌基因文库(L.克拉克和J.卡尔本,《细胞》9:91 - 99,1976)中的至少三个克隆含有gin互补功能。我们将此功能命名为pin,它催化相邻DNA中1800个碱基对的倒位。这个名为P区的可倒位区域,连同pin,进一步亚克隆到pBR322上。接合和转导实验将pin基因定位在大肠杆菌染色体上位置25附近的purB和fabD基因之间。同样位于该区域的是e14,一种隐蔽的、紫外线可切除的遗传元件(A.格林纳和C.W.希尔,《细菌学杂志》144:312 - 321,1980)。我们证明pin和P区是e14的一部分。通过体内遗传操作技术将e14元件克隆到pBR322上。它具有缺陷前噬菌体的特性,包含整合和切除功能以及一个对SOS敏感的阻遏物。