Hills Louise V, Nouri Sara, Slater Howard R
Genetic Health Services Victoria, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville 3052, Australia.
Chromosome Res. 2003;11(4):359-63. doi: 10.1023/a:1024096024847.
Investigation of marker chromosomes is one of the most challenging areas of clinical cytogenetics, especially in the prenatal scenario. A range of techniques including microdissection/reverse painting, SKY and M-FISH are available for the investigation of larger markers (>3 Mb). All these techniques rely on hybridization of unique, homologous sequences with simultaneous suppression of repeat sequences. In contrast, RxFISH is based on hybridization of cross-species syntenic sequences; repeat sequences do not hybridize due to species divergence. We have used RxFISH to analyse a group of the smallest, i.e. minute, supernumerary marker chromosomes. Our results suggest that even the smallest marker chromosomes often contain conserved pericentric euchromatin. More detailed characterization of pericentric genetic content is needed to assess the clinical significance of minute supernumerary markers.
标记染色体的研究是临床细胞遗传学中最具挑战性的领域之一,尤其是在产前诊断的情况下。一系列技术,包括显微切割/反向染色体涂染、光谱核型分析(SKY)和多色荧光原位杂交(M-FISH),可用于研究较大的标记(>3 Mb)。所有这些技术都依赖于独特同源序列的杂交,同时抑制重复序列。相比之下,RxFISH基于跨物种同线序列的杂交;由于物种差异,重复序列不会杂交。我们使用RxFISH分析了一组最小的,即微小的额外标记染色体。我们的结果表明,即使是最小的标记染色体通常也含有保守的着丝粒周围常染色质。需要对着丝粒周围遗传内容进行更详细的表征,以评估微小额外标记的临床意义。