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通过缺失作图对Y连锁DNA探针进行区域定位及其与X染色体和常染色体序列的同源性

Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences.

作者信息

Affara N A, Florentin L, Morrison N, Kwok K, Mitchell M, Cook A, Jamieson D, Glasgow L, Meredith L, Boyd E

出版信息

Nucleic Acids Res. 1986 Jul 11;14(13):5353-73. doi: 10.1093/nar/14.13.5353.

Abstract

A series of Y recombinants have been isolated from Y-specific DNA libraries and regionally located on the Y chromosome using a Y deletion panel constructed from individuals carrying structural abnormalities of the Y chromosome. Of twenty recombinants examined twelve have been assigned to Yp and eight to Yq. Five of the Yp recombinants map between Yp11.2 and Ypter and one can only be assigned to Yp. Of the former, four detect homologies on the X chromosome between Xq13 and Xq24 and the latter one between Xp22.3 and Xpter. The sixth recombinant detects autosomal homologous sequences. The six remaining Yp probes are located between Ycen and Yp11.2. One of these detects a homology on the X chromosome at Xq13-Xq24 and a series of autosomal sequences, two detect uniquely Y-specific sequences and three a complex pattern of autosomal homologies. The remaining eight recombinants have been assigned to three intervals on Yq. Of three recombinants located between Ycen and Yq11.21 two detect only Y sequences and one additional autosomal homologies. Two recombinants lie in the interval Yq11.21-Yq11-22, one of which detects only Y sequences and the other an Xp homology between Xp22.3 and Xpter. Finally, the three remaining Yq recombinants all detect autosomal homologies and are located between Yq11.22 and Yq12. The divergence between homologies on different chromosomes has been examined for three recombinants by washing Southern Blots at different levels of stringency. Additionally, Southern analysis of DNA from flow sorted chromosomes has been used to identify autosomes carrying homologies to two of the Y recombinants.

摘要

已从Y特异性DNA文库中分离出一系列Y重组体,并使用由携带Y染色体结构异常的个体构建的Y缺失图谱将其定位在Y染色体上。在所检测的20个重组体中,12个被定位到Yp,8个被定位到Yq。5个Yp重组体定位于Yp11.2和Ypter之间,1个只能定位到Yp。在前者中,4个在Xq13和Xq24之间检测到X染色体上的同源性,后者在Xp22.3和Xpter之间检测到同源性。第6个重组体检测到常染色体同源序列。其余6个Yp探针位于Ycen和Yp11.2之间。其中1个在Xq13 - Xq24处检测到X染色体上的同源性以及一系列常染色体序列,2个仅检测到独特的Y特异性序列,3个检测到复杂的常染色体同源性模式。其余8个重组体被定位到Yq上的3个区间。在位于Ycen和Yq11.21之间的3个重组体中,2个仅检测到Y序列,1个还检测到额外的常染色体同源性。2个重组体位于Yq11.21 - Yq11 - 22区间,其中1个仅检测到Y序列,另1个在Xp22.3和Xpter之间检测到Xp同源性。最后,其余3个Yq重组体均检测到常染色体同源性,且位于Yq11.22和Yq12之间。通过在不同严格程度下洗涤Southern印迹,检测了3个重组体在不同染色体上同源性之间的差异。此外,对流式分选染色体的DNA进行Southern分析,以鉴定携带与2个Y重组体同源性的常染色体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d711/311545/4e9085295a95/nar00282-0236-a.jpg

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