Jong A Y, Campbell J L
Proc Natl Acad Sci U S A. 1986 Feb;83(4):877-81. doi: 10.1073/pnas.83.4.877.
A yeast gene encoding SSB-1, a single-stranded nucleic acid binding protein, has been isolated by screening a lambda gt11 genomic DNA library. The gene is located on a 1.84-kilobase chromosomal Bgl II-BamHI fragment. Yeast strains carrying the high-copy-number vector YEp24 with an SSB1 gene insert overproduce SSB-1 3-fold and SSB-1 mRNA 10-fold. A typical haploid cell contains about 20,000 molecules of SSB-1; thus, the cells can tolerate up to 60,000 copies. Yeast SSB-1 was expressed in Escherichia coli cells by using a phage T7 expression system. Spores containing the gene disrupted at a point within the coding sequence germinate and grow normally; thus, the gene is not essential. Protein blots show that no SSB-1 or novel immunologically related species that might retain SSB-1 activity are present in cells containing the disrupted SSB1 genes. Southern analysis and protein blots suggest the presence in yeast of a second, related, but nonidentical gene and two immunologically related proteins of 55 kDa and 75 kDa.
通过筛选λgt11基因组DNA文库,分离出了一个编码单链核酸结合蛋白SSB - 1的酵母基因。该基因位于一个1.84千碱基的染色体Bgl II - BamHI片段上。携带插入了SSB1基因的高拷贝数载体YEp24的酵母菌株,其SSB - 1的产量会过量产生3倍,SSB - 1 mRNA的产量会过量产生10倍。一个典型的单倍体细胞含有约20,000个SSB - 1分子;因此,这些细胞能够耐受多达60,000个拷贝。通过使用噬菌体T7表达系统,酵母SSB - 1在大肠杆菌细胞中得以表达。含有在编码序列内某一点被破坏的基因的孢子能够正常萌发和生长;因此,该基因并非必需基因。蛋白质印迹显示,在含有被破坏的SSB1基因的细胞中,不存在SSB - 1或可能保留SSB - 1活性的新的免疫相关物种。Southern分析和蛋白质印迹表明,酵母中存在第二个相关但不相同的基因以及两种55 kDa和75 kDa的免疫相关蛋白。