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通过缺失作图以及对X-Y互换雄性和雌性个体的分析对Y特异性序列进行排序。

Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females.

作者信息

Ferguson-Smith M A, Affara N A, Magenis R E

机构信息

Duncan Guthrie Institute of Medical Genetics, University of Glasgow, UK.

出版信息

Development. 1987;101 Suppl:41-50. doi: 10.1242/dev.101.Supplement.41.

Abstract

We have used DNA from 23 patients with Y-chromosome aberrations and 25 patients with presumptive X-Y interchange to map 39 Yp restriction fragments and 37 Yq restriction fragments. In the majority of patients the results are consistent with a standard contiguous order of sequences along the Y chromosome. In 6 of 26 patients (23%) with Yp aberrations and 2 of 17 (12%) with Yq aberrations, exceptions to the consensus order have been observed. These can be accommodated by postulating the presence of inversion polymorphisms. Such variation may occur more commonly on the nonpairing part of the Y chromosome that in other chromosomes owing to the absence of homologous synapsis and recombination in male meiosis. The Y sequence most frequently present in X-Y interchange males was that recognized by GMGY3. 18 of 19 X-Y interchange males had this sequence suggesting that it is the nearest in the series to the TDF locus, and indicating that the latter maps to the distal end of Yp. Several techniques, including in situ hybridization and DNA measurement by flow cytometry, have been used to demonstrate that in X-Y interchange males there is transfer of Y sequences to the distal end of the X chromosome; no mechanism other than X-Y interchange has been demonstrated.

摘要

我们利用了23例Y染色体畸变患者和25例疑似X-Y易位患者的DNA,对39个Yp限制性片段和37个Yq限制性片段进行了定位。在大多数患者中,结果与Y染色体上序列的标准连续顺序一致。在26例Yp畸变患者中有6例(23%),在17例Yq畸变患者中有2例(12%),观察到了与一致顺序的例外情况。这些可以通过假定存在倒位多态性来解释。由于男性减数分裂中缺乏同源联会和重组,这种变异可能在Y染色体的非配对部分比在其他染色体上更常见。在X-Y易位男性中最常出现的Y序列是被GMGY3识别的序列。19例X-Y易位男性中有18例具有该序列,这表明它在该系列中最接近睾丸决定因子(TDF)基因座,并表明后者定位于Yp的远端。已经使用了包括原位杂交和流式细胞术DNA测量在内的几种技术来证明,在X-Y易位男性中,Y序列转移到了X染色体的远端;除了X-Y易位外,没有证明其他机制。

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