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46,XX男性中的异形X染色体:X-Y易位参与的证据

Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.

作者信息

Evans H J, Buckton K E, Spowart G, Carothers A D

出版信息

Hum Genet. 1979 May 23;49(1):11-31. doi: 10.1007/BF00277683.

Abstract

G- and R-banded chromosome preparations from eight of twelve 46,XX males, with no evidence of mosaicism or a free Y chromosome, were distinguished in blind trials from preparations from normal 46,XX females by virtue of heteromorphism of the short arm of one X chromosome. Photographic measurements on X chromosomes and on chromosome pair 7 in cells from twelve 46,XX males, eight 46,XX females, and four 46,XY males revealed a significant increase in the size of the p arm of one X chromosome in the group of XX males, independently characterised as being heteromorphic for Xp. No such differences were observed between X chromosomes of normal males and females or between homologues of chromosome pair 7 in all groups. The heteromorphism in XX males is a consequence of an alteration in shape (banding profile) and length of the tip of the short arm of one X chromosome, and the difference in size of the two Xp arms in these 46,XXp+ males ranged from 0.4% to 22.9%. From various considerations, including the demonstration of a Y-specific DNA fragment in DNA digests from nuclei of one of three XX males tested, it is concluded that the Xp+ chromosome is a product of Xp-Yp exchange. These exchanges are assumed to originate at meiosis in the male parent and may involve an exchange of different amounts of material. The consequences of such unequal exchange are considered in terms of the inheritance of genes located on Yp and distal Xp. No obvious phenotypic difference was associated with the presence or absence of Xp+. Thus, some males diagnosed as 46,XX are mosaic for a cryptic Y-containing cell line, and there is now excellent evidence that maleness in others may be a consequence of an autosomal recessive gene. The present data imply that in around 70% of 46,XX males, maleness is a consequence of the inheritance of a paternal X-Y interchange product.

摘要

在十二名46,XX男性中,有八名男性的染色体标本经G显带和R显带处理,未发现嵌合体或游离Y染色体的迹象。在盲法试验中,通过一条X染色体短臂的异态性,可将这些男性的染色体标本与正常46,XX女性的标本区分开来。对十二名46,XX男性、八名46,XX女性和四名46,XY男性细胞中的X染色体和第7号染色体对进行摄影测量,结果显示,XX男性组中一条X染色体的p臂大小显著增加,其特征为Xp异态。在正常男性和女性的X染色体之间,或所有组中第7号染色体对的同源染色体之间,均未观察到此类差异。XX男性中的异态性是由于一条X染色体短臂末端的形状(带型)和长度发生改变所致,在这些46,XXp+男性中,两条Xp臂的大小差异在0.4%至22.9%之间。综合各种因素,包括在三名接受检测的XX男性之一的细胞核DNA消化物中发现Y特异性DNA片段,得出结论:Xp+染色体是Xp-Yp交换的产物。这些交换被认为起源于父本减数分裂,可能涉及不同数量物质的交换。从位于Yp和远端Xp上的基因遗传角度考虑了这种不等交换的后果。Xp+的存在与否未伴有明显的表型差异。因此,一些被诊断为46,XX的男性是含有隐匿性Y细胞系的嵌合体,现在有充分证据表明,其他男性的男性特征可能是常染色体隐性基因的结果。目前的数据表明,在约70%的46,XX男性中,男性特征是父本X-Y互换产物遗传的结果。

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