Welcker A J, de Montigny J, Potier S, Souciet J L
Laboratoire de Microbiologie et de Génétique, UPRES-A 7010, Université Louis-Pasteur/CNRS, Strasbourg, 67083, France.
Genetics. 2000 Oct;156(2):549-57. doi: 10.1093/genetics/156.2.549.
Chromosomal rearrangements, such as deletions, duplications, or Ty transposition, are rare events. We devised a method to select for such events as Ura(+) revertants of a particular ura2 mutant. Among 133 Ura(+) revertants, 14 were identified as the result of a deletion in URA2. Of seven classes of deletions, six had very short regions of identity at their junctions (from 7 to 13 bp long). This strongly suggests a nonhomologous recombination mechanism for the formation of these deletions. The total Ura(+) reversion rate was increased 4.2-fold in a rad52Delta strain compared to the wild type, and the deletion rate was significantly increased. All the deletions selected in the rad52Delta context had microhomologies at their junctions. We propose two mechanisms to explain the occurrence of these deletions and discuss the role of microhomology stretches in the formation of fusion proteins.
染色体重排,如缺失、重复或Ty转座,是罕见事件。我们设计了一种方法来筛选此类事件,即特定ura2突变体的尿嘧啶营养缺陷型(Ura(+))回复突变体。在133个Ura(+)回复突变体中,有14个被鉴定为URA2缺失的结果。在七类缺失中,有六类在其连接处具有非常短的同源区域(7至13个碱基对长)。这强烈表明这些缺失的形成是通过非同源重组机制。与野生型相比,rad52Delta菌株中的总Ura(+)回复率提高了4.2倍,且缺失率显著增加。在rad52Delta背景下筛选出的所有缺失在其连接处都有微同源性。我们提出两种机制来解释这些缺失的发生,并讨论微同源性延伸在融合蛋白形成中的作用。