首页> 美国卫生研究院文献>The Journal of Experimental Medicine >MUTANTS OF NONPRODUCER CELL LINES TRANSFORMED BY MURINE SARCOMA VIRUS
【2h】

MUTANTS OF NONPRODUCER CELL LINES TRANSFORMED BY MURINE SARCOMA VIRUS

机译:大量由鼠肉瘤病毒转化的非生产细胞株

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BALB/3T3 cells transformed by the Kirsten sarcoma virus (nonvirus producer BALB/3T3 cells) and mutant cell lines derived therefrom by treatment with bromodeoxyuridine (BrdU) were analyzed for expression of virus-specific RNA using single-stranded DNA transcripts of Rauscher leukemia virus (RLV), a virus activated in one of the cell lines (58-2T), and Ki-SV-specific DNA transcript; the latter transcript after removal of all sequences cross-reactive with RLV RNA. The Rauscher virus DNA detected multiple copies of viral RNA in virus-producing cells (∼2.5 x 103/cell) whether infected with RLV or activated to produce virus with BrdU. Nonproducer (NP) cells and normal BALB cells showed small numbers of RNA genomes (70–250/cell) and only partial saturation of the transcript. The intracellular RNA sedimented at 35S (main peak) with a variable minor peak at 20S with the exception of one mutant cell, M-43-2 (main peak at 26–27S). The 58-2T transcript reacted preferentially in NP cells and their derivatives with biphasic kinetics suggesting the possibility of sequences specific for the original transforming virus. The size of Ki-SV specific sequences were 30S in mutant cells whether or not complete virus was being produced and independent of in vivo transplantability.
机译:使用Rauscher白血病病毒的单链DNA转录本分析了由Kirsten肉瘤病毒转化的BALB / 3T3细胞(非病毒生产者BALB / 3T3细胞)和通过溴脱氧尿苷(BrdU)处理而衍生的突变细胞系,以分析病毒特异性RNA的表达。 (RLV),一种在细胞系(58-2T)中激活的病毒和Ki-SV特异性DNA转录本;删除所有与RLV RNA交叉反应的序列后的转录物。无论是被RLV感染还是被BrdU激活以产生病毒,Rauscher病毒DNA都能在产生病毒的细胞(〜2.5 x 10 3 /细胞)中检测到多个病毒RNA拷贝。非生产者(NP)细胞和正常BALB细胞显示少量的RNA基因组(70-250 /细胞),并且转录本仅部分饱和。细胞内RNA在35S(主峰)处沉淀,在20S处有一个可变的次要峰,除了一个突变细胞M-43-2(26-27S处的主峰)外。 58-2T转录本在NP细胞及其衍生物中具有双相动力学优先反应,表明可能存在特定于原始转化病毒的序列。无论是否正在产生完整的病毒,且独立于体内移植性,突变细胞中Ki-SV特异性序列的大小均为30S。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号