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Emergence of complex rearrangements at translocation breakpoints in a transgenic mouse; implications for mechanisms involved in the formation of chromosome rearrangements

机译:转基因小鼠中易位断点处的复杂重排的出现;对染色体重排形成机制的影响

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Cryptic complex rearrangements as a result of a reciprocal chromosome translocation have been characterised in a transgenic mouse strain. Analysis of the breakpoint junctions in our previous studies showed that the ada transgene was integrated at the breakpoint forming a fusion gene with Golga3 (Mea2). In this study, further detailed analysis around the translocation junctions revealed that the surrounding regions were composed of 13 fragments of defined transgenic chromosome origins over approximately 1.9-Mb areas. Exactly the same cluster structure of these 13 breakpoint fragments already existed in the second generation of the transgenic mice. Our results show that this highly complex rearrangement has been conserved as the incipient form without any additional changes for 18 years up to the present generation, suggesting simultaneous occurrence of multiple events in the founder mouse. Copyright (C) 2007 S. Karger AG, Basel.
机译:互易染色体易位导致的隐秘复杂重排已在转基因小鼠品系中表征。在我们先前的研究中对断点连接的分析表明,ada转基因在断点处整合,形成了与Golga3(Mea2)的融合基因。在这项研究中,有关易位连接点的进一步详细分析显示,周围区域由大约1.9 Mb区域内定义的转基因染色体起源的13个片段组成。在第二代转基因小鼠中已经存在这13个断点片段的完全相同的簇结构。我们的结果表明,这种高度复杂的重排形式一直被保留为起始形式,直到现在这一代一直保持18年没有任何其他变化,这表明在创始小鼠中同时发生了多个事件。版权所有(C)2007 S.Karger AG,巴塞尔。

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