Liehr Thomas, Heller Anita, Starke Heike, Rubtsov Nikolai, Trifonov Vladimir, Mrasek Kristin, Weise Anja, Kuechler Alma, Claussen Uwe
Institute of Human Genetics and Anthropology, Kollegiengasse 10, D-07740 Jena, Germany.
Int J Mol Med. 2002 Apr;9(4):335-9.
The multicolor-banding (MCB) approach allows the differentiation of chromosome region specific areas at the band and sub-band level and is based on region-specific microdissection libraries producing changing fluorescence intensity ratios along the chromosomes. The latter are used to assign different pseudocolors to specific chromosomal regions. We present the complete set of 138 region-specific microdissection libraries for the entire human genome and the resulting MCB patterns for all human chromosomes at the 450-550 band level. In the present work, the creation and handling of the microdissection libraries is detailed for the first time. Additionally, the unique possibilities of the MCB technique to adjust the pseudocolor bands according to the necessities of the studied case is presented in exemplarity. In conclusion, the MCB-technique is a high resolution alternative to other FISH based chromosome banding approaches and suited to clarify, which changes appeared in complex chromosomal rearrangements.
多色带(MCB)方法能够在带和亚带水平区分染色体区域特异性区域,它基于区域特异性显微切割文库,这些文库会产生沿染色体变化的荧光强度比率。后者用于为特定染色体区域分配不同的伪颜色。我们展示了针对整个人类基因组的138个区域特异性显微切割文库的完整集合,以及在450 - 550带水平下所有人类染色体的MCB模式。在本研究中,首次详细介绍了显微切割文库的创建和处理过程。此外,还示例性地展示了MCB技术根据所研究病例的需求调整伪颜色带的独特可能性。总之,MCB技术是一种高分辨率的替代方法,可替代其他基于荧光原位杂交(FISH)的染色体带型分析方法,适用于阐明复杂染色体重排中出现的变化。