Connelly J C, Leach D R
Institute of Cell and Molecular Biology, University of Edinburgh, UK.
Genes Cells. 1996 Mar;1(3):285-91. doi: 10.1046/j.1365-2443.1996.23024.x.
Long DNA palindromes have the potential to adopt hairpin or cruciform secondary structures that inhibit DNA replication. In Escherichia coli, this palindrome-mediated inviability results from the activity of the sbcC and sbcD genes, and genetic observations have suggested that they may encode a nuclease. Mutations in these genes also restore the defect in genetic recombination associated with recBC sbcB mutants.
We have purified the E. coli SbcCD protein from an overexpressing strain and have shown that it has an ATP-dependent DNA double-strand exonuclease activity. Co-purification of nuclease with protein, antibody inhibition and the absence of activity in extracts lacking the sbcCD genes confirm that the activity is intrinsic to SbcCD. The purified protein also has an ATP-independent single-strand DNA endonuclease activity.
We have shown that sbcCD encodes a nuclease. The purified protein has double-strand DNA exonuclease and single-strand DNA endonuclease activities. We propose that SbcCD cleaves secondary structures formed at replication forks and that the broken forks can be repaired by homologous recombination.
长DNA回文序列有可能形成抑制DNA复制的发夹或十字形二级结构。在大肠杆菌中,这种回文序列介导的致死性是由sbcC和sbcD基因的活性导致的,遗传学观察表明它们可能编码一种核酸酶。这些基因中的突变也能恢复与recBC sbcB突变体相关的遗传重组缺陷。
我们从一个过表达菌株中纯化了大肠杆菌SbcCD蛋白,并表明它具有ATP依赖的DNA双链外切核酸酶活性。核酸酶与蛋白质的共纯化、抗体抑制以及缺乏sbcCD基因的提取物中无活性,证实了该活性是SbcCD所固有的。纯化的蛋白还具有ATP非依赖的单链DNA内切核酸酶活性。
我们已经表明sbcCD编码一种核酸酶。纯化的蛋白具有双链DNA外切核酸酶和单链DNA内切核酸酶活性。我们提出SbcCD切割在复制叉处形成的二级结构,并且断裂的叉可以通过同源重组进行修复。