Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Pool-Zobel B L, Claussen U, Liehr T
Institute of Human Genetics and Anthropology, University of Jena, Jena, Germany.
Cytogenet Genome Res. 2003;103(1-2):34-9. doi: 10.1159/000076286.
Multicolor chromosome banding (MCB) using one single chromosome-specific MCB probe set per experiment was previously reported as powerful tool in molecular cytogenetics for the characterization of all kinds of human marker chromosomes. However, a quick analysis of karyotypes with highly complex chromosomal changes was hampered by the problem that up to 24 MCB experiments were necessary for a comprehensive karyotype description. To overcome that limitation the 138 available region-specific microdissection-derived libraries for all human chromosomes were combined to one single probe set, called multitude MCB (mMCB). A typical fluorescence banding pattern along the human karyotype is produced, which can be evaluated either by transforming these profiles into chromosome region-specific pseudo-colors or more reliably by studying the fluorescence profiles. The mMCB probe set has been applied on chromosomes of normal male and female probands, two primary myelodysplastic syndromes and two solid tumor cell lines. Additionally, a cell line of Gorilla gorilla (GGO) studied previously by single chromosome-specific MCB was reevaluated by the mMCB method. All results were in concordance with those obtained in parallel or by other cytogenetic and molecular cytogenetic approaches indicating that mMCB is a powerful multicolor FISH banding tool for fast characterization of complex karyotypes.
先前报道,每次实验使用一套单一的染色体特异性多色染色体带(MCB)探针组是分子细胞遗传学中用于鉴定各类人类标记染色体的有力工具。然而,由于全面描述核型需要多达24次MCB实验,这一问题阻碍了对具有高度复杂染色体变化的核型进行快速分析。为克服这一限制,将所有人类染色体的138个可用区域特异性显微切割文库组合成一套单一的探针组,称为多组MCB(mMCB)。由此产生了一种沿人类核型的典型荧光带型,可通过将这些图谱转换为染色体区域特异性伪彩色来评估,或者通过研究荧光图谱进行更可靠的评估。mMCB探针组已应用于正常男性和女性先证者、两种原发性骨髓增生异常综合征以及两种实体瘤细胞系的染色体。此外,先前通过单一染色体特异性MCB研究的大猩猩(GGO)细胞系也通过mMCB方法进行了重新评估。所有结果均与通过平行或其他细胞遗传学和分子细胞遗传学方法获得的结果一致,表明mMCB是一种用于快速鉴定复杂核型的强大多色荧光原位杂交带型工具。