Lengauer C, Speicher M R, Popp S, Jauch A, Taniwaki M, Nagaraja R, Riethman H C, Donis-Keller H, D'Urso M, Schlessinger D
Institut für Humangenetik und Anthropologie, Heidelberg, Germany.
Hum Mol Genet. 1993 May;2(5):505-12. doi: 10.1093/hmg/2.5.505.
Colored chromosome staining patterns, termed chromosomal 'bar codes' (CBCs), were obtained on human chromosomes by fluorescence in situ hybridization (FISH) with pools of Alu-PCR products from YAC clones containing human DNA inserts ranging from 100 kbp to 1 Mbp. In contrast to conventional G- or R-bands, the chromosomal position, extent, individual color and relative signal intensity of each 'bar' could be modified depending on probe selection and labeling procedures. Alu-PCR amplification products were generated from 31 YAC clones which mapped to 37 different chromosome bands. For multiple color FISH, Alu-PCR amplification products from various clones were either biotinylated or labeled with digoxigenin. Probes from up to twenty YAC clones were used simultaneously to produce CBCs on selected human chromosomes. Evaluation using a cooled CCD camera and digital image analysis confirmed the high reproducibility of the bars from one metaphase spread to another. Combinatorial FISH with mixtures of whole chromosomes paint probes was applied to paint seven chromosomes simultaneously in different colors along with a set of YAC clones which map to these chromosomes. We discuss the potential to construct analytical chromosomal bar codes adapted to particular needs of cytogenetic investigations and automated image analysis.
通过用来自包含100 kbp至1 Mbp人类DNA插入片段的酵母人工染色体(YAC)克隆的Alu-PCR产物池进行荧光原位杂交(FISH),在人类染色体上获得了称为染色体“条形码”(CBC)的彩色染色体染色模式。与传统的G带或R带不同,每个“条带”的染色体位置、范围、个体颜色和相对信号强度可根据探针选择和标记程序进行修改。从31个定位到37个不同染色体带的YAC克隆中产生了Alu-PCR扩增产物。对于多色FISH,来自不同克隆的Alu-PCR扩增产物用生物素或地高辛配基进行标记。同时使用多达20个YAC克隆的探针在选定的人类染色体上产生CBC。使用冷却的电荷耦合器件(CCD)相机和数字图像分析进行评估,证实了从一个中期铺片到另一个中期铺片条带的高重复性。将全染色体涂染探针混合物的组合FISH应用于同时用不同颜色涂染七条染色体以及一组定位到这些染色体的YAC克隆。我们讨论了构建适用于细胞遗传学研究和自动图像分析特定需求的分析性染色体条形码的潜力。