Piette J, Yaniv M
Nucleic Acids Res. 1986 Dec 22;14(24):9595-611. doi: 10.1093/nar/14.24.9595.
The fine contacts of a mouse nuclear factor, called PEB1, with the B enhancer of polyoma virus were analyzed. It protects against DNaseI attack a region of about 50 base pairs that can be divided in two domains. The first contains a GC-rich palindrome and the homology to the SV40 enhancer. The second is homologous to a sequence in the immunoglobulin (Ig) heavy chain gene enhancer. Methylation interference and protection experiments reveal strong specific contacts only with a purine rich track on the late coding strand of the early proximal part of the palindrome. Deletion analysis show that the minimal sequences necessary for binding include only the first domain. The Ig homology contributes only weakly to the binding. The minimal core is similar to the core of the B enhancer defined in vivo. The interactions we observe here are reminiscent of those of TFIIIA positive transcription factor and the 5SRNA gene of Xenopus.
对一种名为PEB1的小鼠核因子与多瘤病毒B增强子的精细接触进行了分析。它能保护一段约50个碱基对的区域免受DNaseI攻击,该区域可分为两个结构域。第一个结构域包含一个富含GC的回文序列以及与SV40增强子的同源性。第二个结构域与免疫球蛋白(Ig)重链基因增强子中的一个序列同源。甲基化干扰和保护实验表明,只有与回文序列早期近端部分晚期编码链上富含嘌呤的序列存在强烈的特异性接触。缺失分析表明,结合所需的最小序列仅包括第一个结构域。Ig同源性对结合的贡献较弱。最小核心与体内定义的B增强子核心相似。我们在此观察到的相互作用让人联想到非洲爪蟾TFIIIA阳性转录因子与5S RNA基因的相互作用。