Kennedy Gregory, Sugden Bill
McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Mol Cell Biol. 2003 Oct;23(19):6901-8. doi: 10.1128/MCB.23.19.6901-6908.2003.
Transient-transfection assays have been used to identify transcription factors, and genetic analyses of these factors can allow a dissection of their mechanism of activation. Epstein-Barr nuclear antigen 1 (EBNA-1) has been shown to activate transcription from transfected templates, but its ability to activate transcription from nuclear templates has been controversial. We have established cells with integrated EBNA-1-responsive templates and have shown that EBNA-1 activates transcription from these chromatin-embedded templates dose dependently. A mutational analysis of EBNA-1 has identified a domain required for transcriptional activation of integrated templates, but not of transfected templates. The ability of EBNA-1 to activate transcription from both integrated and transfected templates can be inhibited by a derivative of EBNA-1 lacking the amino acids required for activation from integrated templates. EBNA-1's mode of activating transfected templates is therefore genetically distinct from that acting on integrated templates.
瞬时转染分析已被用于鉴定转录因子,对这些因子的遗传分析能够剖析它们的激活机制。爱泼斯坦-巴尔核抗原1(EBNA-1)已被证明可激活转染模板的转录,但其激活核模板转录的能力一直存在争议。我们建立了含有整合的EBNA-1反应性模板的细胞,并表明EBNA-1可剂量依赖性地激活这些嵌入染色质模板的转录。对EBNA-1的突变分析确定了整合模板转录激活所需的一个结构域,但转染模板不需要该结构域。EBNA-1从整合模板和转染模板激活转录的能力可被一种缺乏从整合模板激活所需氨基酸的EBNA-1衍生物抑制。因此,EBNA-1激活转染模板的模式在遗传上与作用于整合模板的模式不同。