Hughes K T, Gaines P C, Karlinsey J E, Vinayak R, Simon M I
Department of Microbiology, University of Washington, Seattle 98195.
EMBO J. 1992 Jul;11(7):2695-705. doi: 10.1002/j.1460-2075.1992.tb05335.x.
The Hin recombinase of Salmonella catalyzes a site-specific recombination event which leads to flagellar phase variation. Starting with a fully symmetrical recombination site, hixC, a set of 40 recombination sites which vary by pairs of single base substitutions was constructed. This set was incorporated into the Salmonella-specific bacteriophage P22 based challenge phage selection and used to define the DNA sequence determinants for the binding of Hin to DNA in vivo. The critical sequence-specific contacts between a Hin monomer and a 13 bp hix half-site are at two T:A base pairs in the major groove of the DNA which are separated by one base pair, and two consecutive A:T contacts in the minor groove. The base substitutions in the major groove recognition portion which were defective in binding Hin still retained residual binding capability in vivo, while the base pair substitutions affecting the minor groove recognition region lost all in vivo binding. Using in vitro binding assays, Hin was found to bind to hix symmetrical sites with A:T base pairs or I:C base pairs in the minor groove recognition sequences, but not to G:C base pairs. In separate in vitro binding assays, Hin was equally defective in binding to either a G:C or a I:C contact in a major groove recognition sequence. Results from in vitro binding assays to hix sites in which 3-deazaadenine was substituted for adenine are consistent with Hin making a specific contact to either the N3 of adenine or O2 of thymine in the minor groove within the hix recombination site on each symmetric half-site. These results taken with the results of previous studies on the DNA binding domain of Hin suggest a sequence-specific minor groove DNA binding motif.
沙门氏菌的Hin重组酶催化位点特异性重组事件,该事件导致鞭毛相变。从完全对称的重组位点hixC开始,构建了一组40个通过单碱基替换对而变化的重组位点。该组被整合到基于沙门氏菌特异性噬菌体P22的挑战噬菌体选择中,并用于确定体内Hin与DNA结合的DNA序列决定因素。Hin单体与13 bp hix半位点之间关键的序列特异性接触位于DNA大沟中的两个T:A碱基对处,它们被一个碱基对隔开,以及小沟中的两个连续A:T接触。在体内,大沟识别部分中与Hin结合有缺陷的碱基替换仍保留残余结合能力,而影响小沟识别区域的碱基对替换则失去了所有体内结合能力。通过体外结合试验发现,Hin能与小沟识别序列中具有A:T碱基对或I:C碱基对的hix对称位点结合,但不能与G:C碱基对结合。在单独的体外结合试验中,Hin在与大沟识别序列中的G:C或I:C接触结合时同样存在缺陷。用3-脱氮腺嘌呤替代腺嘌呤的hix位点进行体外结合试验的结果表明,Hin在每个对称半位点的hix重组位点内的小沟中与腺嘌呤的N3或胸腺嘧啶的O2发生特异性接触。这些结果与先前关于Hin的DNA结合结构域的研究结果表明存在一个序列特异性的小沟DNA结合基序。