Corrette-Bennett S E, Mohlman N L, Rosado Z, Miret J J, Hess P M, Parker B O, Lahue R S
The Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Box 986805, Omaha, NE 68198-6805, USA.
Nucleic Acids Res. 2001 Oct 15;29(20):4134-43. doi: 10.1093/nar/29.20.4134.
Small looped mispairs are efficiently corrected by mismatch repair. The situation with larger loops is less clear. Repair activity on large loops has been reported as anywhere from very low to quite efficient. There is also uncertainty about how many loop repair activities exist and whether any are conserved. To help address these issues, we studied large loop repair in Saccharomyces cerevisiae using in vivo and in vitro assays. Transformation of heteroduplexes containing 1, 16 or 38 nt loops led to >90% repair for all three substrates. Repair of the 38 base loop occurred independently of mutations in key genes for mismatch repair (MR) and nucleotide excision repair (NER), unlike other reported loop repair functions in yeast. Correction of the 16 base loop was mostly independent of MR, indicating that large loop repair predominates for this size heterology. Similarities between mammalian and yeast large loop repair were suggested by the inhibitory effects of loop secondary structure and by the role of defined nicks on the relative proportions of loop removal and loop retention products. These observations indicate a robust large loop repair pathway in yeast, distinct from MR and NER, and conserved in mammals.
小的环状错配可通过错配修复有效校正。较大环状结构的情况则不太明确。关于大环状结构的修复活性,报道的范围从非常低到相当高效不等。对于存在多少种环状修复活性以及是否有任何活性是保守的,也存在不确定性。为了帮助解决这些问题,我们使用体内和体外试验研究了酿酒酵母中的大环状修复。含有1、16或38个核苷酸环状结构的异源双链体转化后,所有三种底物的修复率均>90%。与酵母中其他报道的环状修复功能不同,38个碱基环状结构的修复独立于错配修复(MR)和核苷酸切除修复(NER)的关键基因突变发生。16个碱基环状结构的校正大多独立于MR,表明对于这种大小的异源序列,大环状修复占主导。环状二级结构的抑制作用以及特定切口对环状切除产物和环状保留产物相对比例的作用表明了哺乳动物和酵母大环状修复之间的相似性。这些观察结果表明酵母中存在一种强大的大环状修复途径,它不同于MR和NER,并且在哺乳动物中是保守的。