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高变微小卫星区域是人类减数分裂时发生交叉的位点。

Hypervariable minisatellite regions are sites for crossing-over at meiosis in man.

作者信息

Chandley A C, Mitchell A R

机构信息

MRC Human Gentics Unit, Western General Hospital, Edinburgh.

出版信息

Cytogenet Cell Genet. 1988;48(3):152-5. doi: 10.1159/000132613.

Abstract

In situ hybridization to human meiotic metaphase I (MI) preparations, using the labeled minisatellite core sequence lambda 33.15, showed clustering of autoradiographic grains principally at or around chiasmata, autosomal sites where crossing-over had occurred. For the XY bivalent, the pairing region formed between the terminal regions of the two short arms (Xpter Ypter), was also a principal site of labeling; in addition, the terminal region of the X long arm (Xqter) was labeled. Control experiments using a member of the human Alu family of dispersed repeated DNA sequences showed a much more randomized grain distribution, with clustering over chiasmata being far less obvious. The data provide support for the suggestion that polymorphic minisatellite regions within the human genome might play a significant role in pairing and/or recombination.

摘要

使用标记的小卫星核心序列λ33.15对人类减数分裂中期I(MI)的制片进行原位杂交,结果显示放射自显影片上的银粒主要聚集在交叉点处或其周围,交叉点是常染色体上发生交换的位点。对于XY二价体,在两条短臂(Xpter Ypter)末端区域之间形成的配对区域也是主要的标记位点;此外,X长臂的末端区域(Xqter)也有标记。使用人类分散重复DNA序列Alu家族的一个成员进行的对照实验显示,银粒分布更为随机,交叉点处的聚集远不那么明显。这些数据支持了这样一种观点,即人类基因组内的多态性小卫星区域可能在配对和/或重组中发挥重要作用。

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