Subramanian T, Malstrom S E, Chinnadurai G
Institute for Molecular Virology, St. Louis University Medical Center, Missouri 63110.
Oncogene. 1991 Jul;6(7):1171-3.
We have previously reported that adenovirus E1a mutants lacking the C-terminal 61 or 67 amino acids were severely defective in immortalization, but cooperated more efficiently (than wt E1a) with activated T24 ras oncogene in transformation of primary rat kidney (BRK) cells (Subramanian et al., 1989; Oncogene, 4:415-420). Here, we show that in contrast to these previous results, transformation of BRK cells in cooperation with the Ad2 E1b region is dependent on the C-terminal region of E1a. Mutational analysis of the C-terminal region has revealed that a region located between residues 266 and 276 may be important for E1a/E1b cooperative transformation. Like E1a/T24 ras cooperative transformation, E1a/E1b cooperative transformation also requires two essential domains involved in the binding of two cellular proteins (300K and 105K) within the N-terminal half of E1a. E1a/E1b cooperative transformation therefore requires an additional E1a activity encoded within the C-terminal region of E1a.
我们先前曾报道,缺失C末端61或67个氨基酸的腺病毒E1a突变体在永生化方面存在严重缺陷,但在原代大鼠肾(BRK)细胞的转化过程中,与活化的T24 ras癌基因的协同作用更为有效(比野生型E1a)(Subramanian等人,1989年;《癌基因》,4:415 - 420)。在此,我们表明,与这些先前的结果相反,与Ad2 E1b区域协同作用对BRK细胞的转化依赖于E1a的C末端区域。对C末端区域的突变分析表明,位于266和276位残基之间的区域可能对E1a/E1b协同转化很重要。与E1a/T24 ras协同转化一样,E1a/E1b协同转化也需要E1a N末端一半区域内参与结合两种细胞蛋白(300K和105K)的两个必需结构域。因此,E1a/E1b协同转化需要E1a C末端区域编码的额外E1a活性。