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使用Y衍生探针原位杂交对XX男性中Xp-Yp易位的进一步细胞学证据。

Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe.

作者信息

Magenis R E, Casanova M, Fellous M, Olson S, Sheehy R

出版信息

Hum Genet. 1987 Mar;75(3):228-33. doi: 10.1007/BF00281064.

Abstract

Chromosome preparations from seven subjects with aberrations of sex chromosomes were utilized for in situ hybridization studies with the tritium-labeled Y-derived probe p50f. Two subjects had a pseudodicentric chromosome consisting of two copies of Yp and a portion of Y long arm; two were XX males [46,XX,t(Xp;Yp)], one was missing part of the Y short arm, and another had t(5p;Yq); in addition cells from an XYY male as well as a normal 46,XY male, and a 46,XX female, were hybridized with the same probe. The hybridization technique of Harper and Saunders (1981) was used. There was excess labeling of the Yp/paracentromeric regions in the cases with the normal Y, the XYY, the pseudodicentric Y, and the 5/Y translocation. No significant label was seen on metaphases from the normal 46,XX female or the female with the partially missing Y short arm. Excess label was present on the X short arm in the cases of the XX males; there were 8% and 9.5% of cells with label. The combined cytogenetic and hybridization data indicate that one X short arm in these XX males has undergone a translocation with Yp, and that genes for sex determination probably reside on the distal half of the Y short arm.

摘要

利用来自7名性染色体异常患者的染色体标本,与氚标记的Y衍生探针p50f进行原位杂交研究。两名患者有一条假双着丝粒染色体,由两条Yp拷贝和一部分Y长臂组成;两名是XX男性[46,XX,t(Xp;Yp)],一名缺失部分Y短臂,另一名有t(5p;Yq);此外,一名XYY男性以及一名正常46,XY男性和一名46,XX女性的细胞也用同一探针进行杂交。采用了Harper和Saunders(1981)的杂交技术。在具有正常Y、XYY、假双着丝粒Y和5/Y易位的病例中观察到Yp/近着丝粒区域有过量标记。在正常46,XX女性或部分缺失Y短臂的女性的中期相中未观察到明显标记。在XX男性病例中,X短臂上有过量标记;有8%和9.5%的细胞有标记。综合细胞遗传学和杂交数据表明,这些XX男性中的一条X短臂与Yp发生了易位,并且性别决定基因可能位于Y短臂的远端一半。

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