Inamoto S, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
J Biol Chem. 1990 Apr 15;265(11):6461-6.
The traY gene product of plasmid R100 was purified as a hybrid protein, TraY-collagen-beta-galactosidase. The hybrid protein as well as the TraY' protein, which was obtained by collagenolysis of the hybrid protein, specifically binds to an AT-rich 36-base pair sequence (here called sbyA) within the region including the origin of transfer, oriT. The oriT region consists of highly conserved and nonconserved regions among R100-related plasmids, and sbyA was located within the nonconserved region immediately adjacent to the conserved region. This supports the idea that the TraY protein has a role as a component of endonuclease in recognizing its own oriT sequence. Unexpectedly, however, the hybrid protein and the TraY' protein were also found to bind to two different AT-rich sequences (each 24 base pairs in length) in the promoter region preceding the traY gene (here called sbyB and sbyC). This suggests that the TraY protein may have another role in regulating the expression of its own gene. The "TAA(A/T)T" sequence motif observed in these binding sites might constitute a core sequence recognized by the TraY protein. Mg2+ is not required for the specific binding of the TraY protein.
质粒R100的traY基因产物被纯化成为一种融合蛋白,即TraY-胶原蛋白-β-半乳糖苷酶。该融合蛋白以及通过对融合蛋白进行胶原酶解获得的TraY'蛋白,特异性地结合于包括转移起始位点oriT在内的区域内一段富含AT的36碱基对序列(此处称为sbyA)。oriT区域在R100相关质粒中由高度保守区域和非保守区域组成,sbyA位于紧邻保守区域的非保守区域内。这支持了TraY蛋白作为核酸内切酶的一个组分在识别其自身oriT序列中发挥作用的观点。然而,出乎意料的是,还发现该融合蛋白和TraY'蛋白结合于traY基因之前启动子区域的两个不同的富含AT的序列(每个长度为24碱基对)(此处称为sbyB和sbyC)。这表明TraY蛋白可能在调控其自身基因的表达中具有另一个作用。在这些结合位点中观察到的“TAA(A/T)T”序列基序可能构成了TraY蛋白识别的核心序列。TraY蛋白的特异性结合不需要Mg2+。