Fowler R F, Stringfellow L A, Skinner D M
University of Tennessee-Oak Ridge Graduate School of Biomedical Sciences, Biology Division, Oak Ridge National Laboratory 37831.
Gene. 1988 Nov 15;71(1):165-76. doi: 10.1016/0378-1119(88)90088-1.
Sequence analyses show that deletions of 10 and 12 bp occur at homologous sites in a domain that is rich in alternating purines and pyrimidines (Pu/Py) in B42 and EXT, two cloned variants of a complex satellite DNA. A 3-bp deletion occurs 27 bp upstream from the site of the specific deletions in B42 and RU, a third cloned satellite variant that has not suffered the 10-bp deletion. Under torsional stress, the Pu/Py-rich domain adopts a Z-conformation as shown by (i) inhibition of cutting at a BssHII site that accounts for 2/5 of a 15-bp tract of pure Pu/Py in the domain; (ii) binding of polyclonal and monoclonal anti-Z-DNA antibodies to the domain; and (iii) antibody stabilization and subsequent relaxation of the Z-region.
序列分析表明,在复杂卫星DNA的两个克隆变体B42和EXT中,富含交替嘌呤和嘧啶(Pu/Py)的结构域的同源位点发生了10个碱基对和12个碱基对的缺失。在B42和RU(未发生10个碱基对缺失的第三个克隆卫星变体)中,在特定缺失位点上游27个碱基对处发生了3个碱基对的缺失。在扭转应力下,富含Pu/Py的结构域呈现Z构象,这表现为:(i)在一个BssHII位点的切割受到抑制,该位点占该结构域中一段15个碱基对的纯Pu/Py序列的五分之二;(ii)多克隆和单克隆抗Z-DNA抗体与该结构域结合;(iii)抗体使Z区域稳定并随后使其松弛。