作者: A.-L. Lu
DOI: 10.1016/B978-0-12-378630-2.00239-5
关键词: DNA repair 、 Mismatch Repair Pathway 、 Genetics 、 Replication protein A 、 Nucleotide excision repair 、 Base excision repair 、 DNA mismatch repair 、 MutS-1 、 Biology 、 DNA repair protein XRCC4
摘要: There are two major DNA mismatch-repair (MMR) systems in bacteria to correct biosynthetic errors. Long-patch repair involve a long-patch excision and resynthesis (up 1000 nucleotides) specific particular strand. Short-patch have tract shorter than 15 nucleotides, dictated by the nature of mismatches. The methyl-directed MMR distinguishes daughter strand from parental hemi-methylated state enhances fidelity replication genetic recombination. Cells defective several hundred-fold higher spontaneous mutation frequencies transitions short nucleotide insertion/deletion mutations. MMR-defective strains resistant some types alkylating agents. also has an anti-recombination function limiting recombination between divergent sequences preventing gross chromosomal rearrangement. short-patch MutY base pathway is independent methylation. MutY, adenine glycosylase, responsible for reduction errors caused oxidized guanines (8-oxoGs). may be coupled with cooperate mismatch achieve anti-mutagenic functions.