Disteche C M, Saal H, Friedman C, Sybert V, Thuline H
Am J Hum Genet. 1986 May;38(5):751-8.
Sex-chromosome mosaicism was quantitatively analyzed in two patients using DNA probes specific for human X and Y chromosomes. Both patients were female with stigmata of the Turner syndrome, and both had a 45,X cell line and a 46,XY cell line. One of the patients had a morphologically abnormal, nonfluorescent Y chromosome, dic(Y)(q11). Hybridization of DNA from this patient with two repetitive DNA sequences specific for the heterochromatic region of the Y chromosome indicated that most of the Y-heterochromatic sequences were deleted. DNA from both patients was hybridized with a probe for the DXYS1 locus and found to have the X- and Y-linked loci. Densitometric measurements of the relative intensities of the X- and Y-linked bands were used to calculate the degree of mosaicism in each case. The percentages of 45,X cells obtained by DNA analysis agreed with those obtained by chromosome analysis. DNA analysis provides a way to quantitate mosaicism at the DNA level and in nondividing tissue.
使用针对人类X和Y染色体的特异性DNA探针,对两名患者的性染色体嵌合体进行了定量分析。两名患者均为女性,具有特纳综合征的体征,且都有一个45,X细胞系和一个46,XY细胞系。其中一名患者有一条形态异常、无荧光的Y染色体,即双着丝粒Y染色体(dic(Y)(q11))。该患者的DNA与两条针对Y染色体异染色质区域的重复DNA序列杂交,结果表明大部分Y异染色质序列缺失。两名患者的DNA均与DXYS1位点的探针杂交,发现同时具有X和Y连锁位点。通过对X和Y连锁条带相对强度的光密度测量,计算出每种情况下的嵌合程度。通过DNA分析获得的45,X细胞百分比与染色体分析结果一致。DNA分析为在DNA水平和非分裂组织中定量嵌合体提供了一种方法。