Sung Jung-Suk, Demple Bruce
Department of Life Science, Dongguk University, Seoul, South Korea.
FEBS J. 2006 Apr;273(8):1620-9. doi: 10.1111/j.1742-4658.2006.05192.x.
Base excision DNA repair (BER) is fundamentally important in handling diverse lesions produced as a result of the intrinsic instability of DNA or by various endogenous and exogenous reactive species. Defects in the BER process have been associated with cancer susceptibility and neurodegenerative disorders. BER funnels diverse base lesions into a common intermediate, apurinic/apyrimidinic (AP) sites. The repair of AP sites is initiated by the major human AP endonuclease, Ape1, or by AP lyase activities associated with some DNA glycosylases. Subsequent steps follow either of two distinct BER subpathways distinguished by repair DNA synthesis of either a single nucleotide (short-patch BER) or multiple nucleotides (long-patch BER). As the major repair mode for regular AP sites, the short-patch BER pathway removes the incised AP lesion, a 5'-deoxyribose-5-phosphate moiety, and replaces a single nucleotide using DNA polymerase (Polbeta). However, short-patch BER may have difficulty handling some types of lesions, as shown for the C1'-oxidized abasic residue, 2-deoxyribonolactone (dL). Recent work indicates that dL is processed efficiently by Ape1, but that short-patch BER is derailed by the formation of stable covalent crosslinks between Ape1-incised dL and Polbeta. The long-patch BER subpathway effectively removes dL and thereby prevents the formation of DNA-protein crosslinks. In coping with dL, the cellular choice of BER subpathway may either completely repair the lesion, or complicate the repair process by forming a protein-DNA crosslink.
碱基切除DNA修复(BER)在处理因DNA内在不稳定性或各种内源性和外源性活性物质产生的多种损伤方面至关重要。BER过程中的缺陷与癌症易感性和神经退行性疾病有关。BER将多种碱基损伤汇聚到一个共同的中间体,即脱嘌呤/脱嘧啶(AP)位点。AP位点的修复由主要的人类AP内切核酸酶Ape1启动,或由与某些DNA糖基化酶相关的AP裂解酶活性启动。随后的步骤遵循两种不同的BER子途径之一,这两种途径通过单核苷酸(短补丁BER)或多个核苷酸(长补丁BER)的修复DNA合成来区分。作为常规AP位点的主要修复模式,短补丁BER途径去除切割后的AP损伤,即5'-脱氧核糖-5-磷酸部分,并使用DNA聚合酶(Polbeta)替换单个核苷酸。然而,短补丁BER在处理某些类型的损伤时可能会遇到困难,如C1'-氧化的无碱基残基2-脱氧核糖内酯(dL)所示。最近的研究表明,dL能被Ape1有效处理,但短补丁BER会因Ape1切割后的dL与Polbeta之间形成稳定的共价交联而受阻。长补丁BER子途径能有效去除dL,从而防止DNA-蛋白质交联的形成。在应对dL时,细胞对BER子途径的选择可能要么完全修复损伤,要么通过形成蛋白质-DNA交联使修复过程复杂化。