Schaack J, Ho W Y, Tolman S, Ullyat E, Guo X, Frank N, Freimuth P I, Roovers D J, Sussenbach J S
Department of Microbiology, University of Colorado Health Sciences Center, Denver, Colorado, USA.
J Virol. 1999 Nov;73(11):9599-603. doi: 10.1128/JVI.73.11.9599-9603.1999.
Adenoviruses containing lethal in-frame insertion mutant alleles of the preterminal protein (pTP) gene were constructed with cell lines that express pTP. Thirty in-frame insertion mutant alleles, including 26 alleles previously characterized as lethal and 4 newly constructed mutant alleles, were introduced into the viral chromosome in place of the wild-type pTP gene. The viruses were tested for ability to form plaques at 37 degrees C in HeLa-pTP cells and at 32 degrees C and 39.5 degrees C in HeLa cells. Two of the newly constructed viruses exhibited temperature sensitivity for plaque formation, one virus did not form plaques in the absence of complementation, seven additional mutants exhibited a greater than 10-fold reduction in plaque formation in the absence of complementation, and another eight mutants exhibited stronger phenotypes than did previously characterized in-frame insertion mutants in the plaque assay. These mutant viruses offer promise for analysis of pTP functions.
利用表达前末端蛋白(pTP)的细胞系构建了含有pTP基因致死性读框内插入突变等位基因的腺病毒。将30个读框内插入突变等位基因(包括26个先前被鉴定为致死性的等位基因和4个新构建的突变等位基因)导入病毒染色体,取代野生型pTP基因。检测这些病毒在HeLa-pTP细胞中于37℃以及在HeLa细胞中于32℃和39.5℃形成噬斑的能力。新构建的两种病毒表现出噬斑形成的温度敏感性,一种病毒在没有互补作用时不形成噬斑,另外七种突变体在没有互补作用时噬斑形成减少超过10倍,还有八种突变体在噬斑测定中表现出比先前鉴定的读框内插入突变体更强的表型。这些突变病毒为分析pTP功能提供了希望。