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人类α-珠蛋白基因簇的重组:序列特征与拓扑限制

Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.

作者信息

Nicholls R D, Fischel-Ghodsian N, Higgs D R

出版信息

Cell. 1987 May 8;49(3):369-78. doi: 10.1016/0092-8674(87)90289-3.

Abstract

We have characterized 170 kb of DNA around the human alpha-globin gene cluster to enable a systematic analysis of 12 naturally occurring deletions from this region. In 8 deletions, the 3' breakpoints lie within a 6-8 kb segment of DNA, identifying a breakpoint cluster region. Members of the Alu family of repetitive sequences are frequently found at the breakpoints and we describe a novel deletion due to homologous recombination between such repeats. In another deletion the breakpoints are separated by 131 bp of DNA, which we have shown to be transposed from a region 36 kb upstream from the 5' breakpoint where it is present in the inverse orientation. The sizes of these deletions, the nonrandom distribution of their breakpoints, and the nature of the inversion-duplication transposition event suggest that these rearrangements are constrained by the higher-order structure of the alpha-globin cluster.

摘要

我们对人类α-珠蛋白基因簇周围170 kb的DNA进行了特征分析,以便对该区域12个自然发生的缺失进行系统分析。在8个缺失中,3'断点位于一段6 - 8 kb的DNA片段内,确定了一个断点簇区域。在断点处经常发现重复序列的Alu家族成员,我们描述了一种由于此类重复序列之间的同源重组导致的新型缺失。在另一个缺失中,断点被131 bp的DNA隔开,我们已证明该DNA是从5'断点上游36 kb处的一个区域反向转座而来。这些缺失的大小、断点的非随机分布以及反向重复转座事件的性质表明,这些重排受到α-珠蛋白基因簇高阶结构的限制。

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