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46,XX 真两性畸形患者的 Y 染色体性别决定区(SRY)

Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditism.

作者信息

Tanoue A, Nakamura T, Endo F, Nishiyama S, Sakiyama H, Matsuda I

机构信息

Department of Pediatrics, Kumamoto University Medical School, Japan.

出版信息

Jpn J Hum Genet. 1992 Dec;37(4):311-20. doi: 10.1007/BF01883323.

Abstract

Using a polymerase chain reaction method, a search for Y-specific DNA sequences was made in samples derived from tissues of a 46,XX true hermaphrodite. We found a sequence of SRY in the ovotestis, skin and leukocytes. Other DNA sequences, which covered the pseudoautosomal boundary region, amelogenin gene and DYZ1 locus of Y-chromosome were not detected. The SRY gene detected in the patient by the polymerase chain reaction was not detected by Southern blot analysis, using the SRY fragment as a probe. These findings suggest that in the patient there is a mosaicism of cells with and without part of the Y chromosome, including the SRY sequence. As the SRY sequence was responsible for the development of the gonadal primordium to the ovotestis, SRY seems essential for gonadal differentiation in testis development.

摘要

采用聚合酶链反应方法,在一名46,XX真两性畸形患者的组织样本中寻找Y特异性DNA序列。我们在卵睾、皮肤和白细胞中发现了SRY序列。未检测到覆盖Y染色体假常染色体边界区域、牙釉蛋白基因和DYZ1位点的其他DNA序列。用SRY片段作为探针进行Southern印迹分析,未检测到通过聚合酶链反应在患者中检测到的SRY基因。这些发现表明,该患者存在含有和不含有部分Y染色体(包括SRY序列)的细胞嵌合体。由于SRY序列负责性腺原基发育为卵睾,SRY似乎对睾丸发育中的性腺分化至关重要。

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