Percival-Smith A, Segall J
Mol Cell Biol. 1984 Jan;4(1):142-50. doi: 10.1128/mcb.4.1.142-150.1984.
A differential hybridization screen has been used to identify genes cloned from the yeast Saccharomyces cerevisiae that are expressed preferentially during sporulation. Duplicate copies of a partial Sau3A yeast DNA library prepared in the vector pBR322 were hybridized with radioactive cDNA probes representing the mRNA populations of sporulating a alpha cells and asporogenous alpha alpha cells at various times after transfer to sporulation medium. Thirty-eight clones showed an enhanced hybridization signal with the a alpha sporulation probe relative to the alpha alpha control cDNA probe. A comparison of the array of fragments produced by restriction endonuclease digestion of these plasmids suggested that 15 different sequences had been cloned. An RNA blot analysis using these cloned DNAs to probe RNAs purified from aa, a alpha, and alpha alpha cells harvested either during vegetative growth or at 10 h after transfer to sporulation medium indicated that 14 different sporulation-specific genes had been identified. Transcripts complementary to these genes are present only in a alpha cells after transfer to sporulation medium. Three of these clones contain two sporulation-specific genes. Three genes have been identified that are expressed in all cell types during vegetative growth and only in a alpha cells in sporulation medium.
一种差异杂交筛选方法已被用于鉴定从酿酒酵母中克隆的、在孢子形成过程中优先表达的基因。在载体pBR322中制备的部分Sau3A酵母DNA文库的重复拷贝,与代表转移到孢子形成培养基后不同时间的产孢aα细胞和不产孢αα细胞的mRNA群体的放射性cDNA探针进行杂交。相对于αα对照cDNA探针,38个克隆与aα孢子形成探针显示出增强的杂交信号。对这些质粒经限制性内切酶消化产生的片段阵列进行比较表明,已克隆出15种不同的序列。使用这些克隆的DNA探测从营养生长期间或转移到孢子形成培养基10小时后收获的aa、aα和αα细胞中纯化的RNA的RNA印迹分析表明,已鉴定出14个不同的孢子形成特异性基因。与这些基因互补的转录本仅在转移到孢子形成培养基后的aα细胞中存在。这些克隆中有三个包含两个孢子形成特异性基因。已鉴定出三个基因,它们在营养生长期间在所有细胞类型中表达,而在孢子形成培养基中仅在aα细胞中表达。