Hayday A, Gandini-Attardi D, Fried M
Gene. 1981 Oct;15(1):53-65. doi: 10.1016/0378-1119(81)90104-9.
A simple technique is described that allows mixed populations of eukaryotic cells to be screened for clones containing multiple copies of a particular DNA. Essentially, eukaryotic cells are transferred to either nitrocellulose of Whatman 541 filters, and their DNA is immobilised in situ. Exposure of the filters to a 32P-labeled DNA "probe" results in detectable hybridisation only at the positions of clones containing multiple copies of the DNA. Using Whatman 541 paper, a portion of the cells, evenly distributed throughout the mixed population is retained on the culture dish, and can be propagated further for subsequent cell cloning. The technique has allowed rapid distinction of clones of transformed rat cells that contain a single or only a few copies per cell of polyoma viral DNA from clones maintaining multiple copies. The technique has also been used to distinguish between clones of mouse L-cells containing multiple and only a few copies of 0X174 DNA. In this manner the technique allows rapid detection of cells amplifying a particular species of DNA. Finally, the method can be used to detect cells assimilating many copies of a foreign DNA, even in the absence of a co-transfected selectable marker.
本文描述了一种简单的技术,可用于筛选含有特定DNA多拷贝的真核细胞克隆混合群体。实质上,将真核细胞转移至硝酸纤维素膜或Whatman 541滤膜上,其DNA在原位固定。将滤膜与32P标记的DNA“探针”杂交,仅在含有该DNA多拷贝的克隆位置可检测到杂交信号。使用Whatman 541滤纸时,均匀分布于混合群体中的一部分细胞保留在培养皿上,并可进一步传代用于后续细胞克隆。该技术能够快速区分每细胞含有单拷贝或仅少数拷贝多瘤病毒DNA的转化大鼠细胞克隆与维持多拷贝的克隆。该技术还用于区分含有多拷贝和仅少数拷贝0X174 DNA的小鼠L细胞克隆。通过这种方式,该技术可快速检测扩增特定种类DNA的细胞。最后,即使在没有共转染选择标记的情况下,该方法也可用于检测摄取许多拷贝外源DNA的细胞。