Harrison C J, Gibbons B, Yang F, Butler T, Cheung K L, Kearney L, Dirscherl L, Bray-Ward P, Gregson M, Ferguson-Smith M
Department of Haematology, Royal Free and University College Medical School, London, United Kingdom.
Cancer Genet Cytogenet. 2000 Jan 15;116(2):105-10. doi: 10.1016/s0165-4608(99)00116-8.
Exciting new techniques in molecular cytogenetics--namely, spectral karyotyping, multiplex fluorescence in situ hybridization (M-FISH), and cross species color banding--have been recently developed. An increasing number of reports demonstrate the success of these procedures in providing additional cytogenetic information--identifying marker chromosomes and revealing the presence of previously undetected chromosomal changes. However, these procedures have their limitations, and their absolute sensitivity in the accurate identification of subtle chromosomal abnormalities remains to be established. M-FISH and color banding have been applied to a case of chronic myeloid leukemia with a complex Philadelphia translocation involving chromosomes 9, 17, and 22, which had initially been identified from G-banded chromosome analysis. The abnormalities were confirmed by chromosome "painting" and specific probes. Although M-FISH and color banding revealed no additional cryptic chromosomal changes, this study has clearly demonstrated the success of these multiple color FISH approaches in the accurate characterization of a complex rearrangement with subtle abnormalities.
分子细胞遗传学领域令人兴奋的新技术——即光谱核型分析、多重荧光原位杂交(M-FISH)和跨物种染色体显带技术——最近已被开发出来。越来越多的报告表明,这些方法在提供额外的细胞遗传学信息方面取得了成功,如识别标记染色体和揭示先前未检测到的染色体变化。然而,这些方法有其局限性,其在准确识别细微染色体异常方面的绝对敏感性仍有待确定。M-FISH和染色体显带技术已应用于一例慢性髓性白血病患者,该患者存在涉及9号、17号和22号染色体的复杂费城染色体易位,最初是通过G显带染色体分析确定的。这些异常通过染色体“描绘”和特异性探针得到了证实。尽管M-FISH和染色体显带技术未发现其他隐匿性染色体变化,但这项研究清楚地证明了这些多色FISH方法在准确表征伴有细微异常的复杂重排方面的成功。