Lill N L, Tevethia M J, Eckner R, Livingston D M, Modjtahedi N
Division of Neoplastic Disease Mechanisms, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 1997 Jan;71(1):129-37. doi: 10.1128/JVI.71.1.129-137.1997.
Several cellular polypeptides critical for growth regulation interact with DNA tumor virus oncoproteins. p400 is a cellular protein which binds to the adenovirus E1A oncoprotein(s). The biological function of p400 is not yet known, but it is structurally and immunologically closely related to p300 and CREB-binding protein, two known E1A-binding transcription adapters. Like p300, p400 is a phosphoprotein that binds to the simian virus 40 large tumor antigen (T). In anti-T coimmunoprecipitation experiments, staggered deletions spanning the amino-terminal 250 amino acids of T did not abrogate T binding to either p400 or p300. A T species composed of residues 251 to 708 bound both p400 and p300, while a T species defective in p53 binding was unable to bind either detectably. Anti-p53 immunoprecipitates prepared from cells containing wild-type T also contained p400 and p300. Hence, both p400 and p300 can bind (directly or indirectly) to a carboxyl-terminal fragment of T which contains its p53 binding domain. Since the p53 binding domain of T contributes to its immortalizing and transforming activities, T-p400 and/or T-p300 interactions may participate in these functions.
几种对生长调节至关重要的细胞多肽与DNA肿瘤病毒癌蛋白相互作用。p400是一种与腺病毒E1A癌蛋白结合的细胞蛋白。p400的生物学功能尚不清楚,但它在结构和免疫方面与p300及CREB结合蛋白密切相关,这两种蛋白是已知的E1A结合转录衔接蛋白。与p300一样,p400是一种磷酸化蛋白,可与猿猴病毒40大肿瘤抗原(T)结合。在抗T共免疫沉淀实验中,跨越T氨基末端250个氨基酸的交错缺失并未消除T与p400或p300的结合。由251至708位残基组成的T物种与p400和p300都结合,而在p53结合方面有缺陷的T物种则无法检测到结合。从含有野生型T的细胞制备的抗p53免疫沉淀物中也含有p400和p300。因此,p400和p300都可以(直接或间接)与T的一个羧基末端片段结合,该片段包含其p53结合结构域。由于T的p53结合结构域有助于其永生化和转化活性,T-p400和/或T-p300相互作用可能参与这些功能。