Program of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Biochemistry. 2013 Feb 5;52(5):773-85. doi: 10.1021/bi301369b. Epub 2013 Jan 22.
Expansions of (CTG)·(CAG) repeated DNAs are the mutagenic cause of 14 neurological diseases, likely arising through the formation and processing of slipped-strand DNAs. These transient intermediates of repeat length mutations are formed by out-of-register mispairing of repeat units on complementary strands. The three-way slipped-DNA junction, at which the excess repeats slip out from the duplex, is a poorly understood feature common to these mutagenic intermediates. Here, we reveal that slipped junctions can assume a surprising number of interconverting conformations where the strand opposite the slip-out either is fully base paired or has one or two unpaired nucleotides. These unpaired nucleotides can also arise opposite either of the nonslipped junction arms. Junction conformation can affect binding by various structure-specific DNA repair proteins and can also alter correct nick-directed repair levels. Junctions that have the potential to contain unpaired nucleotides are repaired with a significantly higher efficiency than constrained fully paired junctions. Surprisingly, certain junction conformations are aberrantly repaired to expansion mutations: misdirection of repair to the non-nicked strand opposite the slip-out leads to integration of the excess slipped-out repeats rather than their excision. Thus, slipped-junction structure can determine whether repair attempts lead to correction or expansion mutations.
(CTG)·(CAG)重复 DNA 的扩展是 14 种神经疾病的诱变原因,可能是通过形成和处理滑动链 DNA 而产生的。这些重复突变的瞬态中间产物是由互补链上重复单元的错配引起的。三链滑动 DNA 连接点是双链体中多余重复序列滑出的位置,是这些诱变中间体的一个未被充分理解的共同特征。在这里,我们揭示了滑动连接点可以假设许多相互转化的构象,其中滑出的互补链完全碱基配对或有一个或两个未配对的核苷酸。这些未配对的核苷酸也可以出现在非滑动连接臂的任一侧。连接点构象可以影响各种结构特异性 DNA 修复蛋白的结合,也可以改变正确的缺口定向修复水平。具有潜在未配对核苷酸的连接点的修复效率明显高于受约束的完全配对连接点。令人惊讶的是,某些连接点构象会异常修复为扩展突变:修复的错误定向到滑出的非缺口链导致多余滑出的重复序列的整合而不是它们的切除。因此,滑动连接点结构可以决定修复尝试是导致纠正还是扩展突变。