Goedecke W, Pfeiffer P, Vielmetter W
Insitut for Genetics, Cologne, Germany.
Nucleic Acids Res. 1994 Jun 11;22(11):2094-101. doi: 10.1093/nar/22.11.2094.
Cells of higher eucaryotes are known to possess mechanisms of illegitimate recombination which promote the joining between nonhomologous ends of broken DNA and thus may serve as basic tools of double-strand-break (DSB) repair. Here we show that cells of the fission yeast Schizosaccharomyces pombe also contain activities of nonhomologous DNA end joining resembling the ones found in higher eucaryotes. Nonhomologous end joining activities were detected by transformation of linearized self-replicating plasmids in yeast cells employing a selection procedure which only propagates transformants carrying recircularized plasmid molecules. Linear plasmid substrates were generated by duplicate restriction cuts carrying either blunt ends or 3' or 5' protruding single strands (PSS) of 4 nt which were efficiently joined in any tested combination. Sequence analysis of joined products revealed that junctional sequences were shortened by 1 to 14 nt. Two mechanisms may account for junction formation (i) loss of terminal nucleotides from PSS tails to produce blunt ends which can be joined to abutting ends and (ii) interactions of DNA termini at patches of sequence homologies (1-4 bp) by formation of overlap intermediates which are subsequently processed. A general feature of the yeast joining system is that end joining can only be detected in the absence of sequence homology between the linear substrate and host genome. In the presence of homology, nonhomologous DNA end joining is efficiently competed by activities of homologous recombination.
已知高等真核生物的细胞拥有异常重组机制,这种机制促进断裂DNA的非同源末端之间的连接,因此可能作为双链断裂(DSB)修复的基本工具。在此我们表明,裂殖酵母粟酒裂殖酵母的细胞也含有类似于在高等真核生物中发现的非同源DNA末端连接活性。通过在酵母细胞中转化线性化的自我复制质粒来检测非同源末端连接活性,采用一种选择程序,该程序仅繁殖携带环化质粒分子的转化体。线性质粒底物通过重复的限制性切割产生,带有平端或4个核苷酸的3'或5'突出单链(PSS),这些底物在任何测试组合中都能有效连接。连接产物的序列分析表明,连接序列缩短了1至14个核苷酸。两种机制可能解释连接的形成:(i)PSS尾巴末端核苷酸的丢失以产生可与邻接末端连接的平端;(ii)通过形成重叠中间体,DNA末端在序列同源性(1 - 4个碱基对)区域相互作用,随后进行加工。酵母连接系统的一个普遍特征是,只有在线性底物与宿主基因组之间不存在序列同源性时才能检测到末端连接。在存在同源性的情况下,同源重组活性会有效竞争非同源DNA末端连接。