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A hotspot for novel amplification joints in a mosaic of Alu-like repeats and palindromic A + T-rich DNA.

机译:Alu样重复序列和回文A + T丰富的DNA马赛克中新的扩增关节的热点。

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摘要

We have identified, in the amplified domain of adenylate deaminase (AMPD) overproducing Chinese hamster fibroblasts, a 2.6 kb recombinogenic DNA region which is frequently involved in amplification-associated rearrangements. The nucleotide sequence reveals a mosaic organization of four Alu-equivalent repeats of the B1 and B2 families and eight long A + T-rich DNA segments. Part of this region is enriched with long imperfect palindromes. The center of one palindrome contains a putative topoisomerase I cleavage site and this site defines the position of a novel junction which was formed by illegitimate recombination with anther A + T-rich DNA sequence located far apart on the amplified DNA. These findings and their significance are discussed in the context of related data from other systems and in the light of current models for eukaryotic DNA recombination, replication and organization.
机译:我们已经确定,在过量生产的中国仓鼠成纤维细胞的腺苷酸脱氨酶(AMPD)的扩增域中,一个2.6 kb的重组DNA区域经常与扩增相关的重排有关。核苷酸序列揭示了一个马赛克组织,包含四个B1和B2家族的Alu等效重复序列以及八个长的富含A + T的DNA片段。该区域的一部分富含长期不完善的回文。一个回文的中心包含一个推定的拓扑异构酶I切割位点,该位点定义了一个新的连接点的位置,该连接点是通过与富含A + T的DNA序列在重组DNA上相距很远的非法重组而形成的。这些发现及其意义将在其他系统的相关数据的背景下,并根据当前的真核DNA重组,复制和组织模型进行讨论。

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