Chen D S, Bernstein H
Department of Microbiology and Immunology, College of Medicine, University of Arizona, Tucson 85724.
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6821-5. doi: 10.1073/pnas.85.18.6821.
The RAD52 gene of Saccharomyces cerevisiae and genes 46 and 47 of bacteriophage T4 are essential for most recombination and recombinational repair in their respective organisms. The RAD52 gene was introduced into expression vectors that were used to transform Escherichia coli. The expression of RAD52 was then induced, and the ability of RAD52 to complement phage mutants defective in gene 46 or 47 was determined with respect to the three criteria of phage growth, recombination, and recombinational repair. RAD52 gene expression was found to allow growth of gene 46 and 47 mutants under otherwise restrictive conditions, as measured by plaque formation and burst size. Expression of the RAD52 gene also restored the ability of gene 46 and 47 mutants to undergo recombination of rII markers. Furthermore, the RAD52 gene restored the ability of gene 46 and 47 mutants to undergo recombinational repair after UV irradiation. The published DNA sequence of gene RAD52 was compared with the published sequences of genes 46 and 47. Although overall sequence similarities were only marginally significant, RAD52 and gene 46 had substantial sequence similarity over a limited region.
酿酒酵母的RAD52基因以及噬菌体T4的基因46和47对于它们各自生物体中的大多数重组和重组修复至关重要。将RAD52基因导入用于转化大肠杆菌的表达载体中。然后诱导RAD52的表达,并根据噬菌体生长、重组和重组修复这三个标准来确定RAD52对基因46或47有缺陷的噬菌体突变体的互补能力。通过噬菌斑形成和爆发大小来衡量,发现RAD52基因表达能使基因46和47突变体在其他限制性条件下生长。RAD52基因的表达还恢复了基因46和47突变体进行rII标记重组的能力。此外,RAD52基因恢复了基因46和47突变体在紫外线照射后进行重组修复的能力。将已发表的RAD52基因DNA序列与已发表的基因46和47的序列进行比较。尽管总体序列相似性仅略有显著性,但RAD52和基因46在有限区域内有相当大的序列相似性。