Casati A, Stefanini M, Giorgi R, Ghetti P, Nuzzo F
Istituto di Genetica Biochimica ed Evoluzionistica CNR-Pavia, Italy.
Cancer Genet Cytogenet. 1991 Jan;51(1):89-101. doi: 10.1016/0165-4608(91)90014-l.
Chromosome analysis was carried out in cultured fibroblasts from unaffected skin of five unrelated xeroderma pigmentosum (XP) patients and nine family members. Structural chromosome changes were observed in cultures from all examined individuals. Furthermore, in one XPD patient and in one XPC patient and his parents, cytogenetically abnormal clones were detected. Some of these clones were present starting from the primary explant. This cytogenetic pattern is similar to that observed in an XPC patient previously studied by us. The analysis of breakpoint distribution from clonal and non-clonal chromosome rearrangements showed that some breakpoints were more frequent and common to different families or to different family members although definite evidence of preferential involvement of chromosome bands was not obtained. This investigation indicates that there is a consistent tendency toward chromosome instability in XP mutation carriers. The instability could be related to the multiple chromosome anomalies characterizing skin tumors in XP subjects.
对5名无关的着色性干皮病(XP)患者及9名家庭成员未受影响皮肤的培养成纤维细胞进行了染色体分析。在所有检测个体的培养物中均观察到染色体结构变化。此外,在1名XPD患者以及1名XPC患者及其父母中,检测到细胞遗传学异常克隆。其中一些克隆从原代外植体开始就存在。这种细胞遗传学模式与我们之前研究的1名XPC患者中观察到的模式相似。对克隆性和非克隆性染色体重排的断点分布分析表明,尽管未获得染色体带优先受累的确切证据,但某些断点在不同家族或不同家庭成员中更频繁且常见。这项研究表明,XP突变携带者存在染色体不稳定的一致倾向。这种不稳定性可能与XP患者皮肤肿瘤所特有的多种染色体异常有关。