Nietzel A, Rocchi M, Starke H, Heller A, Fiedler W, Wlodarska I, Loncarevic I F, Beensen V, Claussen U, Liehr T
Institute of Human Genetics and Anthropology, Jena, Germany.
Hum Genet. 2001 Mar;108(3):199-204. doi: 10.1007/s004390100459.
Centromere-specific multi-color FISH (cenM-FISH) is a new multicolor FISH technique that allows the simultaneous characterization of all human centromeres by using labeled centromeric satellite DNA as probes. This approach allows the rapid identification of all human centromeres by their individual pseudo-coloring in one single step and is therefore a powerful tool in molecular cytogenetics. CenM-FISH fills a gap in multicolor karyotyping using WCP probes and distinguishes all centromeric regions apart from the evolutionary highly conserved regions on the chromosomes 13 and 21. The usefulness of the cenM-FISH technique for the characterization of small supernumerary marker chromosomes with no (or nearly no) euchromatin and restricted amounts of available sample material is demonstrated in prenatal, postnatal, and tumor cytogenetic cases. In addition, rarely described markers with the involvement of heterochromatic material inserted into homogeneously staining regions could be identified and characterized by using the cenM-FISH technique.
着丝粒特异性多色荧光原位杂交(cenM-FISH)是一种新的多色荧光原位杂交技术,它通过使用标记的着丝粒卫星DNA作为探针,能够同时对所有人类着丝粒进行特征分析。这种方法可以通过在一步操作中对所有人类着丝粒进行单独的假彩色标记,从而快速识别它们,因此是分子细胞遗传学中的一种强大工具。CenM-FISH填补了使用全染色体涂染探针进行多色核型分析的空白,并能区分所有着丝粒区域,除了13号和21号染色体上进化上高度保守的区域。cenM-FISH技术在产前、产后和肿瘤细胞遗传学病例中,对于鉴定没有(或几乎没有)常染色质且可用样本材料有限的小额外标记染色体的特征具有实用性。此外,使用cenM-FISH技术可以鉴定和表征很少被描述的、涉及插入均匀染色区域的异染色质物质的标记。