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Isolation of a cDNA encoding the adenovirus E1A enhancer binding protein: a new human member of the ets oncogene family.

机译:编码腺病毒E1A增强子结合蛋白的cDNA的分离:ets癌基因家族的新成员。

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摘要

The cDNA encoding adenovirus E1A enhancer-binding protein E1A-F was isolated by screening a HeLa cell lambda gt11 expression library for E1A-F site-specific DNA binding. One cDNA clone produced recombinant E1A-F protein with the same DNA binding specificity as that endogenous to HeLa cells. Sequence analysis of the cDNA showed homology with the ETS-domain, a region required for sequence-specific DNA binding and common to all ets oncogene members. Analysis of the longest cDNA revealed about a 94% identity in amino acids between human E1A-F and mouse PEA3 (polyomavirus enhancer activator 3), a recently characterized ets oncogene member. E1A-F was encoded by a 2.5kb mRNA in HeLa cells, which was found to increase during the early period of adenovirus infection. In contrast, ets-2 mRNA was significantly reduced in infected HeLa cells. The results indicate that E1A enhancer binding protein E1A-F is a member of the ets oncogene family and is probably a human homologue of mouse PEA3.
机译:通过筛选HeLa细胞λgt11表达文库中的E1A-F位点特异性DNA结合来分离编码腺病毒E1A增强子结合蛋白E1A-F的cDNA。一个cDNA克隆产生的重组E1A-F蛋白具有与HeLa细胞内源性相同的DNA结合特异性。 cDNA的序列分析显示与ETS结构域的同源性,ETS结构域是序列特异性DNA结合所必需的区域,并且是所有et癌基因成员所共有的区域。对最长cDNA的分析显示,人E1A-F和小鼠PEA3(多瘤病毒增强剂激活剂3)是最近发现的ets癌基因成员,在氨基酸上约有94%的一致性。 E1A-F由HeLa细胞中的2.5kb mRNA编码,发现在腺病毒感染的早期阶段E1A-F增加。相反,在感染的HeLa细胞中ets-2 mRNA显着降低。结果表明,E1A增强子结合蛋白E1A-F是ets癌基因家族的成员,可能是小鼠PEA3的人类同源物。

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