Stinchcomb D T, Thomas M, Kelly J, Selker E, Davis R W
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4559-63. doi: 10.1073/pnas.77.8.4559.
A selective scheme is presented for isolating sequences capable of replicating autonomously in the yeast Saccharomyces cerevisiae. YIp5, a vector that contains the yeast gene ura3, does not transform a ura3 deletion mutant to Ura+. Hybrid YIp5-Escherichia coli DNA molecules also fail to produce transformants. However, collections of molecular hybrids between YIp5 and DNA from any of six eukaryotes tested (S. cerevisiae, Neurospora crassa, Dictyostelium discoideum Ceanhorabditis elegans, Drosophila melanogaster, and Zea mays) do transform the deletion mutant. The Ura+ transformants grow slowly, are unstable under nonselective conditions, and carry the transforming DNA as autonomously replicating, supercoiled circular molecules. Such a phenotype is qualitatively identical to that of strains transformed by molecules containing a yeast chromosomal origin of replication. Thus, these DNA hybrid molecules may contain eukaryotic origins of replication. The isolated sequences may be useful in determiing the signals controlling DNA replication in yeast and in studying both DNA replication and transformation in other eukaryotic organisms.
本文提出了一种用于分离能够在酿酒酵母中自主复制的序列的筛选方案。YIp5是一种含有酵母ura3基因的载体,它不能将ura3缺失突变体转化为Ura+。YIp5与大肠杆菌的杂交DNA分子也无法产生转化体。然而,YIp5与所测试的六种真核生物(酿酒酵母、粗糙脉孢菌、盘基网柄菌、秀丽隐杆线虫、黑腹果蝇和玉米)中任何一种的DNA之间的分子杂交体集合确实能转化缺失突变体。Ura+转化体生长缓慢,在非选择性条件下不稳定,并携带作为自主复制的超螺旋环状分子的转化DNA。这种表型与由含有酵母染色体复制起点的分子转化的菌株的表型在性质上是相同的。因此,这些DNA杂交分子可能包含真核生物的复制起点。分离出的序列可能有助于确定控制酵母中DNA复制的信号,并有助于研究其他真核生物中的DNA复制和转化。