Cohen J I, Kieff E
Medical Virology Section, National Institutes of Health, Bethesda, Maryland 20892.
J Virol. 1991 Nov;65(11):5880-5. doi: 10.1128/JVI.65.11.5880-5885.1991.
Epstein-Barr virus nuclear protein 2 (EBNA-2) increases mRNA levels of specific viral and cellular genes through direct or indirect effects on upstream regulatory elements. The EBNA-2 domains essential for these effects have been partially defined and correlate with domains important for B-cell growth transformation. To determine whether EBNA-2 has a direct transcriptional activating domain, gene fusions between the DNA-binding domain of GAL4 and EBNA-2 were tested in CHO and B-lymphoma cells for the ability to activate transcription from target plasmids containing GAL4 recognition sites upstream of an adenovirus or murine mammary tumor virus promoter. In B-lymphoma cells, a 37-amino-acid EBNA-2 domain previously identified to be essential for transformation was nearly as strong a transcriptional activator as the activating domain of herpes simplex virus trans-inducing factor VP16. A quadradecapeptide had about 25% of the activating activity of the longer peptide. This first evidence that EBNA-2 directly activates transcription should facilitate the identification of nuclear factors with which EBNA-2 interacts in transactivation and transformation.
爱泼斯坦-巴尔病毒核蛋白2(EBNA-2)通过对上游调控元件的直接或间接作用,提高特定病毒和细胞基因的mRNA水平。对这些作用至关重要的EBNA-2结构域已部分明确,且与对B细胞生长转化重要的结构域相关。为确定EBNA-2是否具有直接转录激活结构域,在CHO细胞和B淋巴瘤细胞中测试了GAL4的DNA结合结构域与EBNA-2之间的基因融合体,以检测其激活含有腺病毒或小鼠乳腺肿瘤病毒启动子上游GAL4识别位点的靶质粒转录的能力。在B淋巴瘤细胞中,先前确定对转化至关重要的一个37个氨基酸的EBNA-2结构域作为转录激活剂的作用几乎与单纯疱疹病毒反式诱导因子VP16的激活结构域一样强。一个十四肽具有较长肽激活活性的约25%。EBNA-2直接激活转录的这一初步证据应有助于鉴定EBNA-2在反式激活和转化中相互作用的核因子。