Austin C A, Sng J H, Patel S, Fisher L M
Department of Cellular and Molecular Sciences, St George's Hospital Medical School, London, UK.
Biochim Biophys Acta. 1993 Mar 20;1172(3):283-91. doi: 10.1016/0167-4781(93)90215-y.
DNA topoisomerase (topo) II mediates DNA strand passage in an ATP-dependent reaction. Human cell lines express at least two genetically distinct forms of the enzyme, topo II alpha (p170) and II beta (p180). Previously, we isolated a novel HeLa cDNA clone (CAA5) that partially encodes a protein homologous to topo II alpha (Austin, C.A. and Fisher, L.M. (1990) FEBS Lett. 266, 115-117). In this paper we show that CAA5 encodes a C-terminal segment of human topo II beta. We report here for the first time cDNA clones spanning the entire coding sequence. Overlapping clones specifying the 3' end of the cDNA have been isolated, mapped and sequenced. The missing 5' coding sequence was obtained by an inverse PCR protocol and from a specifically primed cDNA library. Human topo II beta is a 1621 amino acid protein which is closely homologous to topo II alpha in the N-terminal three quarters of its sequence. In contrast, the C-terminal segments of the alpha and beta sequences show considerable divergence suggesting these regions may mediate different cellular functions of the two isoforms. Southern blot analysis of yeast and Drosophila DNA using human alpha and beta specific probes detected a single topo II homologue in these lower eukaryotes. Comparison of the protein sequence for human topo II beta with other type II topoisomerases revealed several conserved motifs and has allowed identification of the likely ATPase- and DNA breakage-reunion domains.
DNA拓扑异构酶(topo)II在ATP依赖的反应中介导DNA链的通过。人类细胞系表达至少两种基因上不同的该酶形式,拓扑异构酶IIα(p170)和IIβ(p180)。此前,我们分离出一个新的HeLa cDNA克隆(CAA5),它部分编码一种与拓扑异构酶IIα同源的蛋白质(奥斯汀,C.A.和费舍尔,L.M.(1990年)《欧洲生物化学学会联合会快报》266,115 - 117)。在本文中,我们表明CAA5编码人类拓扑异构酶IIβ的一个C末端片段。我们首次在此报告跨越整个编码序列的cDNA克隆。已经分离、定位并测序了指定cDNA 3'末端的重叠克隆。缺失的5'编码序列通过反向PCR方案并从一个特异引物cDNA文库中获得。人类拓扑异构酶IIβ是一种1621个氨基酸的蛋白质,在其序列的N末端四分之三部分与拓扑异构酶IIα密切同源。相比之下,α和β序列的C末端片段显示出相当大的差异,表明这些区域可能介导这两种同工型的不同细胞功能。使用人类α和β特异性探针对酵母和果蝇DNA进行的Southern印迹分析在这些低等真核生物中检测到单个拓扑异构酶II同源物。将人类拓扑异构酶IIβ的蛋白质序列与其他II型拓扑异构酶进行比较,揭示了几个保守基序,并有助于确定可能的ATP酶和DNA断裂 - 重连结构域。