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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Ku-Dependent and Ku-Independent End-Joining Pathways Lead to Chromosomal Rearrangements During Double-Strand Break Repair in Saccharomyces cerevisiae
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Ku-Dependent and Ku-Independent End-Joining Pathways Lead to Chromosomal Rearrangements During Double-Strand Break Repair in Saccharomyces cerevisiae

机译:Ku依赖和Ku独立的末端连接途径导致酿酒酵母双链断裂修复过程中的染色体重排。

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Chromosomal double-strand breaks (DSBs) can be repaired by either homology-dependent or homology-independent pathways. Nonhomologous repair mechanisms have been relatively less well studied, despite their potential importance in generating chromosomal rearrangements. We have developed a Saccharomyces cerevisiae -based assay to identify and characterize homology-independent chromosomal rearrangements associated with repair of a unique DSB generated within an engineered URA3 gene. Approximately 1% of successfully repaired cells have accompanying chromosomal rearrangements consisting of large insertions, deletions, aberrant gene conversions, or other more complex changes. We have analyzed rearrangements in isogenic wild-type, rad52, yku80, and rad52 yku80 strains, to determine the types of events that occur in the presence or absence of these key repair proteins. Deletions were found in all strain backgrounds, but insertions were dependent upon the presence of Yku80p. A rare RAD52 - and YKU80 -independent form of deletion was present in all strains. These events were characterized by long one-sided deletions (up to 13 kb) and extensive imperfect overlapping sequences (7-22 bp) at the junctions. Our results demonstrate that the frequency and types of repair events depend on the specific genetic context. This approach can be applied to a number of problems associated with chromosome stability.
机译:染色体双链断裂(DSB)可以通过依赖于同源性或依赖于同源性的途径进行修复。尽管非同源修复机制在产生染色体重排中具有潜在的重要性,但其研究相对较少。我们已经开发了一种基于酿酒酵母的测定法,以鉴定和表征与修复工程化的URA3基因内产生的独特DSB相关的不依赖同源性的染色体重排。成功修复的细胞中约有1%具有伴随的染色体重排,包括大的插入,缺失,异常的基因转化或其他更复杂的变化。我们已经分析了同基因野生型,rad52,yku80和rad52 yku80菌株中的重排,以确定在这些关键修复蛋白存在或不存在下发生的事件的类型。在所有菌株背景中均发现缺失,但插入取决于Yku80p的存在。在所有菌株中都存在罕见的RAD52和YKU80独立的缺失形式。这些事件的特征是在连接处长的一侧缺失(最多13 kb)和广泛的不完美重叠序列(7-22 bp)。我们的结果表明,修复事件的频率和类型取决于特定的遗传背景。这种方法可以应用于许多与染色体稳定性有关的问题。

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