Gänshirt-Ahlert D, Pawlowitzki I H, Gal A
Hum Genet. 1987 Jun;76(2):153-6. doi: 10.1007/BF00284913.
Three patients with 45,X/46,XYnf mosaicism were investigated by Southern hybridization using both X- and Y-specific DNA probes. Our patients seem to be hemizygous for the X chromosomal loci tested. Single-copy and low-copy repeated Y chromosomal sequences assigned to the short arm, centromere, and euchromatin of the long arm have been detected in our patients, suggesting the Y chromosomal origin of the marker chromosome both in male and female cases studied. Densitometry of autoradiographs revealed a double dose of Yp-specific fragments of the DXYS1 locus. None of the patients tested showed either the 3.4- or the 2.1-kb Hae III male-specific repeated DNA sequences. It seems likely that the Ynf is a pseudodicentric chromosome with duplication of Yp and euchromatic Yq sequences, the Yq heterochromatin being lost. Our findings indicate structural heterogeneity of the marker chromosome and in addition provide further information on the relative position of DNA sequences detected by DNA probes 50f2, M1A, and pDP105.
对3例45,X/46,XYnf嵌合体患者使用X和Y特异性DNA探针进行了Southern杂交研究。我们的患者在所检测的X染色体位点似乎是半合子。在我们的患者中检测到了定位于Y染色体短臂、着丝粒和长臂常染色质的单拷贝和低拷贝重复Y染色体序列,这表明在所研究的男性和女性病例中,标记染色体均起源于Y染色体。放射自显影片的光密度测定显示DXYS1位点的Yp特异性片段有双倍剂量。所检测的患者均未显示出3.4kb或2.1kb的Hae III男性特异性重复DNA序列。Ynf似乎是一条假双着丝粒染色体,Yp和常染色质Yq序列发生了重复,Yq异染色质丢失。我们的研究结果表明标记染色体存在结构异质性,此外还提供了关于DNA探针50f2、M1A和pDP105所检测到的DNA序列相对位置的进一步信息。