Bernheim A, Metezeau P, Guellaën G, Fellous M, Goldberg M E, Berger R
Proc Natl Acad Sci U S A. 1983 Dec;80(24):7571-5. doi: 10.1073/pnas.80.24.7571.
A method is described for directly hybridizing a small number of sorted chromosomes with specific DNA probes. The chromosomes are analyzed by flow cytometry and sorted by deflecting the droplets containing the desired chromosomes onto a nitrocellulose filter. By using probes specific for the human Y chromosome, it has been possible to unambiguously identify the peak corresponding to the Y chromosome in the flow karyotypes of a variety of male cell lines. The position of this peak was found to vary significantly from individual to individual, correlating with the heterochromatin chromosomal polymorphism of the human Y chromosome. The sensitivity of the hybridization was such that, with a probe for a male-specific repetitive sequence, only 2,500 sorted chromosomes were enough to obtain a clear, positive signal; 10,000 were needed with a probe specific for a weakly repeated (maximum, 3-fold) sequence of Y chromosome. With this new method, chromosome sorting may be a rapid and efficient way to assign DNA sequences to chromosomes.
本文描述了一种将少量分选后的染色体与特定DNA探针直接杂交的方法。通过流式细胞术分析染色体,并通过将含有所需染色体的液滴偏转到硝酸纤维素滤膜上来进行分选。使用针对人类Y染色体的特异性探针,已能够在多种雄性细胞系的流式核型中明确识别出对应于Y染色体的峰。发现该峰的位置在个体之间存在显著差异,这与人类Y染色体的异染色质染色体多态性相关。杂交的灵敏度使得,对于雄性特异性重复序列的探针,仅2500条分选后的染色体就足以获得清晰的阳性信号;对于Y染色体弱重复(最多3倍)序列的特异性探针,则需要10000条。通过这种新方法,染色体分选可能是将DNA序列定位到染色体上的一种快速且高效的方式。