Gemmill R M, Pearce-Birge L, Bixenman H, Hecht B K, Allanson J E
Am J Hum Genet. 1987 Aug;41(2):157-67.
Phenotypic females with Y-chromosomal material in their genome have an increased risk for development of gonadal malignancy. The detection and identification of Y-chromosomal material in these cases can be of critical importance for medical management. Chromosome analysis in four patients with Turner syndrome revealed the characteristic 45,X chromosome complement together with a second cell population containing a small marker chromosome (46,X, + mar). Molecular-hybridization analyses utilizing cloned, Y chromosome-specific DNA sequences were performed to determine whether Y-chromosomal material was present in each patient. Three cases contained some Y chromosome-specific sequences, whereas one case was negative with all four probes that we used. These results were compared with detailed cytogenetic studies--including G-, Q-, and G-11-banding--of the marker chromosomes. In one case in which Y chromosome-specific DNA sequences were demonstrated, the marker chromosome was G-11 negative. These results demonstrate that cytogenetic analysis alone can lead to misidentification of some Y chromosome-derived markers. The combination of cytogenetic and molecular analyses permits a more accurate characterization of anomalous Y chromosomes and in turn provides additional information that can be crucial to the correct medical management of Turner-syndrome patients.
基因组中含有Y染色体物质的表型女性发生性腺恶性肿瘤的风险增加。在这些病例中检测和鉴定Y染色体物质对医疗管理至关重要。对4例特纳综合征患者进行染色体分析,发现其具有特征性的45,X染色体核型,同时还有第二个细胞群体,其中含有一条小的标记染色体(46,X, + mar)。利用克隆的Y染色体特异性DNA序列进行分子杂交分析,以确定每位患者是否存在Y染色体物质。3例含有一些Y染色体特异性序列,而1例对我们使用的所有4种探针均呈阴性。将这些结果与标记染色体的详细细胞遗传学研究(包括G显带、Q显带和G-11显带)进行比较。在1例显示有Y染色体特异性DNA序列的病例中,标记染色体G-11阴性。这些结果表明,仅靠细胞遗传学分析可能会导致对一些Y染色体衍生标记的错误识别。细胞遗传学和分子分析相结合能够更准确地表征异常Y染色体,进而提供对特纳综合征患者正确医疗管理可能至关重要的额外信息。