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A study of the heterogeneous 37s ribonucleic acid induced by foot-and-mouth-disease virus

机译:口蹄疫病毒诱导的异源37s核糖核酸的研究

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摘要

1. The 37s RNA induced in baby-hamster kidney cells by infection with foot-and-mouth-disease virus was examined on sucrose gradients and by filtration through Sepharose 4B. 2. The RNA sedimented faster (37s) and as a broader band than the 35s RNA from purified virus. 3. Treatment with deoxyribonuclease, Pronase or amylase did not alter the sedimentation profile of the 37s RNA. 4. Treatment of individual fractions of the RNA with phenol, dimethyl sulphoxide or methylCellosolve did not decrease the sedimentation rate of the faster-sedimenting molecules. 5. Sedimentation in sucrose gradients of different ionic strengths or containing EDTA had no effect on the heterogeneous nature of the profile. 6. On filtration through Sepharose 4B columns, the 37s virus-induced RNA was eluted before viral RNA. 7. Only 20% of the rapidly sedimenting RNA was incorporated into complete virus particles.
机译:1.在蔗糖梯度上并通过Sepharose 4B过滤,检查了因感染口蹄疫病毒而在仓鼠肾细胞中诱导的37s RNA。 2.与从纯化病毒中提取的35s RNA相比,RNA沉淀的速度更快(37s)且带宽。 3.用脱氧核糖核酸酶,链霉蛋白酶或淀粉酶处理不会改变37s RNA的沉淀特性。 4.用苯酚,二甲基亚砜或甲基溶纤剂处理RNA的各个部分并不会降低沉降速度更快的分子的沉降速率。 5.在不同离子强度或含有EDTA的蔗糖梯度中沉淀不会影响剖面的异质性。 6.通过Sepharose 4B柱过滤时,在病毒RNA之前洗脱37s病毒诱导的RNA。 7.只有20%的快速沉淀RNA被掺入完整的病毒颗粒中。

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