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Y染色体短臂出现新生卫星区,可能源于不稳定易位。

A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

作者信息

Lin C L, Gibson L, Pober B, Yang-Feng T L

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA.

出版信息

Hum Genet. 1995 Nov;96(5):585-8. doi: 10.1007/BF00197415.

Abstract

A satellited long arm of the Y chromosome (Yqs) is considered a normal variation, whereas the presence of a satellite on the short arm of the Y (Yps) has never been described in the literature. A Yps chromosome could be clinically significant if the translocation resulting in Yps has relocated the testis-determining gene, SRY, to another chromosome. A carrier of such a translocation would therefore be at increased risk for having XX male and XY female offspring. Here we describe the first reported case of de novo Yps present in a phenotypically normal male. This Yps chromosome was positive for C-banding and nucleolus organizer region (NOR) staining and showed a hybridization signal for the beta-satellite sequence. Fluorescence in situ hybridization (FISH) analysis indicated that SRY was retained on the Yps and the translocation breakpoint on Yps was distal to the pseudoautosomal region. At prenatal diagnosis, a normal appearing Y chromosome was found in his son, and thus the satellite on Yps was lost during meiotic Xp-Yp pairing. This Yps chromosome was likely the product of an "unstable" translocation.

摘要

Y染色体的卫星长臂(Yqs)被认为是一种正常变异,而Y染色体短臂上出现卫星(Yps)在文献中从未有过描述。如果导致Yps的易位将睾丸决定基因SRY重新定位到另一条染色体上,那么Yps染色体可能具有临床意义。因此,这种易位的携带者生出XX男性和XY女性后代的风险会增加。在此,我们描述了首例报道的表型正常男性中出现的新发Yps病例。这条Yps染色体C带和核仁组织区(NOR)染色呈阳性,并显示出β卫星序列的杂交信号。荧光原位杂交(FISH)分析表明,SRY保留在Yps上,Yps上的易位断点位于假常染色体区域的远端。在产前诊断时,在他儿子身上发现了一条外观正常的Y染色体,因此Yps上的卫星在减数分裂Xp - Yp配对过程中丢失了。这条Yps染色体可能是“不稳定”易位的产物。

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