Keck J G, Feigenbaum F, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Virol. 1993 Oct;67(10):5749-53. doi: 10.1128/JVI.67.10.5749-5753.1993.
Transient transfection assays indicated that A2L is one of three vaccinia virus intermediate genes that are required for the transcriptional transactivation of viral late genes. We have expressed the A2L open reading frame in Escherichia coli and shown by blotting experiments that the 26-kDa protein binds zinc, a property predicted by the presence of a CX2CX13CX2C zinc finger motif. The specificity for zinc binding was demonstrated by competition with other metals. The role of the sequence motif in zinc binding was established by analysis of a series of mutations, including truncations and conservative single amino acid substitutions. Mutations that reduced zinc binding in vitro prevented the ability of A2L to transactivate late genes in vivo.
瞬时转染分析表明,A2L是痘苗病毒晚期基因转录反式激活所需的三个中间基因之一。我们已在大肠杆菌中表达了A2L开放阅读框,并通过印迹实验表明,这种26 kDa的蛋白质能结合锌,这一特性由CX2CX13CX2C锌指基序的存在所预测。通过与其他金属的竞争证明了锌结合的特异性。通过分析一系列突变,包括截短和保守的单氨基酸替换,确定了序列基序在锌结合中的作用。在体外降低锌结合的突变会阻止A2L在体内反式激活晚期基因的能力。