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Detection and characterization of multiple forms of simian virus 40 large T antigen.

机译:猿猴病毒40大T抗原的多种形式的检测和表征。

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摘要

Subclasses of simian virus 40 large T antigen in simian virus 40-transformed and -infected cells separated by zone velocity sedimentation in sucrose density gradients have been characterized. Three forms of large T antigen were distinguished: a 5 to 6S form, a 14 to 16S form, and a 23 to 25S form. These forms appeared to differ biochemically and biologically. Differential labeling experiments suggested that the 5 to 6S form was less highly phosphorylated than the faster-sedimenting forms. The 23 to 25S form which was complexed with one or more host phosphoproteins, as reported recently (D. P. Lane and L. V. Crawford Nature [London] 268:261-263, 1979; F. McCormick and E. Harlow, J. Virol. 34: 213-224, 1980), was prominent in extracts of transformed cells, but was also detected in productively infected cells. Pulse-chase experiments suggested that the 5 to 6S large T antigen is a precursor of the more stable, faster-sedimenting forms of T antigen. Monkey cells infected with a tsA mutant of simian virus 40 at 41 degrees C contained only 5 to 6S large T antigen, implying that this form is not active in the initiation of simian virus 40 DNA replication. In pulse-chase, shift-down experiments, DNA replication resumed, and the 5 to 6S large T antigen which had accumulated at 41 degrees C was partially converted at 33 degrees C to a fast-sedimenting form. However, shift-up experiments demonstrated that the fast-sedimenting large T antigen, once formed, remained stable at 41 degrees C, although it was unable to function in initiation. These experiments suggest that different biological functions of large T antigen may be carried out by different subclasses of this protein.
机译:已经表征了通过蔗糖密度梯度中的区域速度沉降分离的猿猴病毒40转化和感染的细胞中的猿猴病毒40大T抗原的亚类。区分了三种形式的大T抗原:5至6S形式,14至16S形式和23至25S形式。这些形式在生化和生物学上似乎有所不同。差异标记实验表明,5至6S形式的磷酸化程度低于快速沉降形式。最近报道的23至25S形式与一种或多种宿主磷蛋白复合(DP Lane和LV Crawford Nature [伦敦] 268:261-263,1979; F。McCormick和E. Harlow,J。Virol。34: 213-224,1980),在转化细胞的提取物中很显着,但在生产性感染的细胞中也能检测到。脉冲追踪实验表明5至6S的大T抗原是更稳定,沉降更快的T抗原形式的前体。在41摄氏度下被猿猴病毒40的tsA突变体感染的猴细胞仅含有5至6S的大T抗原,这表明这种形式在猿猴病毒40 DNA复制的起始中没有活性。在脉冲追踪,降档实验中,DNA复制恢复,并且在41摄氏度下积累的5至6S大T抗原在33摄氏度下部分转化为快速沉淀形式。但是,升档实验表明,快速沉淀的大T抗原一旦形成,尽管在启动时无法发挥作用,但在41摄氏度时仍保持稳定。这些实验表明,大T抗原的不同生物学功能可以通过该蛋白的不同亚类来实现。

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