Heinzel T, Velleman M, Schuster H
Max-Planck-Institut für Molekulare Genetik, Berlin, F.R.G.
J Mol Biol. 1989 Jan 5;205(1):127-35. doi: 10.1016/0022-2836(89)90370-7.
The repressor of bacteriophage P1, encoded by the c1 gene, represses the phage lytic functions and is responsible for maintaining the P1 prophage in the lysogenic state. The c1 repressor interacts with at least 11 binding sites or operators widely scattered over the P1 genome. From these operators, a 17 base-pair asymmetric consensus sequence, ATTGCTCTAATAAATTT, was derived. Here, we show that the operator, Op72 of the P1ban operon consists of two overlapping 17 base-pair sequences a and b forming an incomplete palindrome. Op72a matches the consensus sequence, whereas Op72b contains two mismatches. The evidence is based on the sequence analysis of 27 operator mutants constitutive for ban expression. They were identified as single-base substitutions at positions 2 to 10 of Op72a (26 mutants) and at position 8 of Op72b (one mutant). We conclude from gel retardation and footprinting studies that two repressor molecules bind to the operator and that positions 4, 5 and 7 to 10 of the operator play an essential role in repressor recognition.
由c1基因编码的噬菌体P1阻遏物可抑制噬菌体的裂解功能,并负责将P1原噬菌体维持在溶原状态。c1阻遏物与广泛分布于P1基因组的至少11个结合位点或操纵基因相互作用。从这些操纵基因中,推导得到了一个17个碱基对的不对称共有序列ATTGCTCTAATAAATTT。在此,我们表明P1ban操纵子的操纵基因Op72由两个重叠的17个碱基对序列a和b组成,形成一个不完全回文结构。Op72a与共有序列匹配,而Op72b包含两个错配。证据基于对27个组成型表达ban的操纵基因突变体的序列分析。它们被鉴定为Op72a第2至10位(26个突变体)和Op72b第8位(1个突变体)的单碱基替换。我们从凝胶阻滞和足迹分析研究中得出结论,两个阻遏物分子与操纵基因结合,并且操纵基因的第4、5位以及第7至10位在阻遏物识别中起关键作用。