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首页> 外文期刊>Journal of Virology >Spontaneous Conversion of Nontransformed Avian Sarcoma Virus-Infected Rat Cells to the Transformed Phenotype
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Spontaneous Conversion of Nontransformed Avian Sarcoma Virus-Infected Rat Cells to the Transformed Phenotype

机译:非转化的非转化禽Sarcoma病毒感染大鼠细胞转化为转化的表型

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Normal rat kidney (NRK) fibroblasts were infected with the Schmidt-Ruppin strain (SR-D) of avian sarcoma virus (ASV) and cloned 20 h after infection without selection for the transformed phenotype. Most infected clones initially exhibited the flat, nontransformed morphology that is characteristic of uninfected NRK cells. In long-term culture, however, the majority of the SR-D NRK clones began segregating typical ASV-transformed cells. Transforming ASV could be rescued by fusion with chicken embryo fibroblasts from most of the infected clones tested. Three predominantly flat, independently infected clones were further analyzed by subcloning 8 to 10 weeks after infection. Most flat progeny subclones derived at random from two of these “parental” SR-D NRK clonal lines did not yield virus upon fusion with chicken embryo fibroblasts, although a nondefective transforming ASV was repeatedly recovered from the parental clones. This observation suggested that most, but not all, daughter cells in these SR-D NRK clones lost the ASV provirus after cloning. The progeny of the third independent parental cell clone, c17, gave rise to both flat and transformed subclones that carried ASV. In this case, ASV recovery by fusion and transfection from the progeny subclones was equally efficient regardless of the transformation phenotype of the cells. The 60,000-dalton phosphoprotein product of the ASV src gene was, however, expressed at high level only in the transformed variants. The results of a Luria-Delbruck fluctuation analysis and of Newcombe's respreading test indicated that the event leading to the spontaneous conversion to the transformed state occurred at random in dividing cultures of these flat ASV NRK cells at a rate predicted for somatic mutation.
机译:正常大鼠肾(NRK)成纤维细胞用禽肉瘤病毒(ASV)的Schmidt-Ruppin菌株(SR-D)感染并在感染后克隆20小时,而不选择转化的表型。大多数感染的克隆最初表现出扁平的非转化形态,其是未感染的NRK细胞的特征。然而,在长期培养中,大多数SR-D NRK克隆开始分离典型的ASV转化细胞。可以通过从大多数受感染的克隆的鸡胚成纤维细胞融合来拯救转化ASV。通过在感染后的8至10周进一步分析三种主要平坦的独立感染的克隆。在这些“父母”SR-D NRK克隆克隆克隆克隆克隆克隆克隆克隆族衍生的大多数扁平后代亚克酮在融合时不会产生病毒,尽管从父母克隆中重复回收裸射转化的ASV。这种观察结果表明,大多数情况下,但不是全部,这些SR-D NRK克隆的女儿细胞在克隆后丧失了ASV潜意。第三个独立亲本细胞克隆C17的后代,使携带ASV的平坦和转化的亚克酮。在这种情况下,无论细胞的转化表型如何,通过融合和从后代亚克酮转染的ASV恢复同样有效。然而,ASV SRC 基因的60,000-Dalton磷蛋白产物仅在转化的变体中以高水平表达。 Luria-Delbruck波动分析和Newcombe的辅助试验结果表明,导致自发转化为转化状态的事件以预测的速率分割这些扁平的ASV NRK细胞的培养物,以预测的是体细胞突变的速率。

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