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Concerted deletions and inversions are caused by mitotic recombination between delta sequences in Saccharomyces cerevisiae.

机译:协同的缺失和倒位是由酿酒酵母中δ序列之间的有丝分裂重组引起的。

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Deletions of a tyrosine tRNA suppressor gene, SUP4-o, are mediated by recombination between short repeated delta sequences in Saccharomyces cerevisiae. The arrangement of the five solo delta sequences that surround the SUP4 locus was established by DNA sequence analysis. Seven deletion classes were identified by genomic blotting. DNA sequence analysis also showed that the delta sequences within a 6.5-kilobase region of the SUP4 locus were the endpoints of these events. In three of these classes, an adjacent interval surrounded by delta sequences was inverted in concert with the deletion. The frequency of all deletion classes decreased in strains that contained mutations in the recombination and repair gene RAD52. We present two gene conversion mechanisms by which these rearrangements could have been generated. These models may also explain deletions between repeated sequences in other systems.
机译:酪氨酸tRNA抑制基因SUP4-o的缺失是通过酿酒酵母中短重复δ序列之间的重组介导的。通过DNA序列分析,确定了围绕SUP4基因座的五个soloδ序列的排列。通过基因组印迹鉴定了七个缺失类别。 DNA序列分析还显示,SUP4基因座的6.5碱基区域内的δ序列是这些事件的终点。在这些类别的三个类别中,与缺失一致地反转了由δ序列包围的相邻间隔。在重组和修复基因RAD52中含有突变的菌株中,所有缺失类别的频率均降低。我们提出了两种基因转换机制,通过这些机制可以产生这些重排。这些模型还可以解释其他系统中重复序列之间的缺失。

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