首页> 美国卫生研究院文献>Journal of Virology >Control of simian virus 40 gene expression at the levels of RNA synthesis and processing: thermally induced changes in the ratio of the simian virus 40 early mRNAs and proteins.
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Control of simian virus 40 gene expression at the levels of RNA synthesis and processing: thermally induced changes in the ratio of the simian virus 40 early mRNAs and proteins.

机译:在RNA合成和加工水平上控制猿猴病毒40基因表达:热诱导猿猴病毒40早期mRNA和蛋白质比例的变化。

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摘要

Examination of the simian virus 40 early mRNA's from infected AGMK or CV-1 cells showed that the ratio of large T- to small t-antigen mRNA's increased with an increased incubation temperature. In tsA58 mutant-infected cells, an increased incubation temperature resulted in the overproduction of early RNAs'; however, the ratio of the early mRNA's was the same, at any temperature, in both wild-type- and tsA58-infected cells. Thus, the thermally induced alteration in the early mRNA ratios was apparently not affected by the tsA mutation or by the overproduction of early RNA in tsA mutant-infected cells. Time course studies at various temperatures showed that, although the ratio of large T- to small t-antigen mRNA's increased with temperature, at any one temperature it was consistent from early to late times of infection. Furthermore, the ratio of the early mRNA's adjusted in temperature shift experiments. Thus, the ratio of the early mRNA's appeared to be intrinsic to the thermodynamic environment of the cell. The thermally induced alterations in the early mRNA's were reflected at the protein level by parallel changes in the ratio of large T- to small t-antigens. These data suggest a level of gene expression control which may function at the stage of splicing.
机译:从感染的AGMK或CV-1细胞中检测猿猴病毒40个早期mRNA,结果表明,随着孵育温度的升高,大T抗原与小T抗原mRNA的比例增加。在tsA58突变体感染的细胞中,温育温度升高导致早期RNA的过量产生。然而,在任何温度下,野生型和tsA58感染的细胞中,早期mRNA的比率均相同。因此,在tsA突变体感染的细胞中,热诱导的早期mRNA比例的改变显然不受tsA突变或早期RNA过量产生的影响。各种温度下的时程研究表明,尽管大T抗原与小T抗原mRNA的比例随温度增加而增加,但在任一温度下,从感染的早期到晚期都是一致的。此外,在温度变化实验中调节了早期mRNA的比例。因此,早期mRNA的比例似乎是细胞热力学环境所固有的。早期mRNA的热诱导改变通过大T抗原与小T抗原的比例的平行变化反映在蛋白质水平上。这些数据表明基因表达控制的水平可能在剪接阶段起作用。

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