Corrette-Bennett S E, Parker B O, Mohlman N L, Lahue R S
Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198-6805, USA.
J Biol Chem. 1999 Jun 18;274(25):17605-11. doi: 10.1074/jbc.274.25.17605.
Single base mispairs and small loops are corrected by DNA mismatch repair, but little is known about the correction of large loops. In this paper, large loop repair was examined in nuclear extracts of yeast. Biochemical assays showed that repair activity occurred on loops of 16, 27, and 216 bases, whereas a G-T mispair and an 8-base loop were poorly corrected under these conditions. Two modes of loop repair were revealed by comparison of heteroduplexes that contained a site-specific nick or were covalently closed. A nick-stimulated repair mode directs correction to the discontinuous strand, regardless of which strand contains the loop. An alternative mode is nick-independent and preferentially removes the loop. Both outcomes of repair were largely eliminated when DNA replication was inhibited, suggesting a requirement for repair synthesis. Excision tracts of 100-200 nucleotides, spanning the position of the loop, were observed on each strand under conditions of limited DNA repair synthesis. Both repair modes were independent of the mismatch correction genes MSH2, MSH3, MLH1, and PMS1, as judged by activity in mutant extracts. Together the loop specificity and mutant results furnish evidence for a large loop repair pathway in yeast that is distinct from mismatch repair.
单碱基错配和小环可通过DNA错配修复来校正,但对于大环的校正了解甚少。在本文中,我们研究了酵母核提取物中的大环修复。生化分析表明,修复活性出现在16、27和216个碱基的环上,而在这些条件下,G-T错配和8个碱基的环校正效果较差。通过比较含有位点特异性切口或共价闭合的异源双链体,揭示了两种环修复模式。切口刺激的修复模式将校正导向不连续链,而不管哪条链含有环。另一种模式是切口非依赖性的,优先去除环。当DNA复制受到抑制时,两种修复结果都大大减少,这表明需要修复合成。在有限的DNA修复合成条件下,在每条链上都观察到了跨越环位置的100-200个核苷酸的切除片段。根据突变提取物中的活性判断,两种修复模式均独立于错配校正基因MSH2、MSH3、MLH1和PMS1。环特异性和突变结果共同为酵母中一种不同于错配修复的大环修复途径提供了证据。