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涉及P因子内重复序列的重排优先发生在靠近转座子末端的单元之间。

Rearrangements involving repeated sequences within a P element preferentially occur between units close to the transposon extremities.

作者信息

Pâques F, Bucheton B, Wegnez M

机构信息

Laboratoire d'Embryologie Moléculaire et Expérimentale, Université Paris XI, Orsay, France.

出版信息

Genetics. 1996 Feb;142(2):459-70. doi: 10.1093/genetics/142.2.459.

DOI:10.1093/genetics/142.2.459
PMID:8852845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1206980/
Abstract

In a previous report we described rearrangements occurring at a high rate (30% of the progeny of dysgenic flies) within a cluster of 5S genes internal to a P element. These events were characterized as precise amplifications and deletions of 5S units. Here we analyze recombination events within P elements containing two repeated arrays of 5S genes flanking a central white gene. Deletions (50%) and duplications (3%) of the white gene together with various amounts of flanking 5S genes were observed. These recombinations occur preferentially between the most external 5S units of P transposons. Such rearrangements could be favored by interactions between the proteins bound to the P terminal sequences.

摘要

在之前的一份报告中,我们描述了在P元件内部的一个5S基因簇内以高频率(不育果蝇后代的30%)发生的重排。这些事件的特征是5S单元的精确扩增和缺失。在这里,我们分析了含有两个重复的5S基因阵列且围绕一个中央白色基因的P元件内的重组事件。观察到白色基因的缺失(50%)和重复(3%)以及不同数量的侧翼5S基因。这些重组优先发生在P转座子最外部的5S单元之间。这种重排可能受到与P末端序列结合的蛋白质之间相互作用的促进。

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Genetics. 1996 Feb;142(2):459-70. doi: 10.1093/genetics/142.2.459.
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本文引用的文献

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Deletions and amplifications of tandemly arranged ribosomal 5S genes internal to a P element occur at a high rate in a dysgenic context.在杂种不育的情况下,P因子内部串联排列的核糖体5S基因的缺失和扩增发生率很高。
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