首页> 美国卫生研究院文献>Journal of Virology >Unique species of mRNA from adenovirus type 7 early region 1 in cells transformed by adenovirus type 7 DNA fragment.
【2h】

Unique species of mRNA from adenovirus type 7 early region 1 in cells transformed by adenovirus type 7 DNA fragment.

机译:在由7型腺病毒DNA片段转化的细胞中来自7型腺病毒早期区域的mRNA的独特种类。

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

Adenovirus type 7 (Ad7) early region 1 mRNA species transcribed in rat cell lines transformed by the HindIII-I . J fragment (the left 7.8% of the viral genome) and in human KB cells infected with Ad7 were mapped on the viral genome, using S1 nuclease gel and diazobenzyloxymethyl paper hybridization techniques. At the early stage of productive infection, two mRNA's (950 and 840 nucleotides long) with the common 5' and 3' ends but different internal splicings were mapped from region 1A (map units 1.4 to 4.3), and one mRNA (2,310 nucleotides long, with the internal splicing between map units 9.9 to 10.1) was mapped from region 1B (map units 4.6 to 11.4). At the late stage, these early spliced mRNA's were also found and at least three additional Ad7 mRNA's were identified: 700-nucleotide-long mRNA in region 1A; and 1,100- and nucleotide-long mRNA's in region 1B. In transformed rat cell lines, two early region 1A mRNA's (950 and 840 nucleotides long) were also transcribed. Surprisingly, in addition, several unique Ad7 mRNA's, not found in productivity infected cells, were identified in all of the transformed cell lines. Their molecular sizes and coding sequences varied in individual cell lines. However, these mRNA's had the 5' end-proximal portion in region 1B and the 3' end-proximal portion in region 1A, these portions being transcribed by extending from region 1B to 1A on viral DNA fragments joined in a tandem array in transformed cells.
机译:在由HindIII-1转化的大鼠细胞系中转录的7型腺病毒(Ad7)早期区域1 mRNA物种。使用S1核酸酶凝胶和重氮苄氧基甲基纸杂交技术,将J片段(病毒基因组的左侧7.8%)和感染Ad7的人KB细胞中的基因定位在病毒基因组上。在生产性感染的早期阶段,从区域1A(映射单元1.4到4.3)定位了两个具有5'和3'末端共同但内部剪接不同的mRNA(长950和840个核苷酸)和一个mRNA(长2310核苷酸)。从区域1B(地图单元4.6至11.4)映射了,其中地图单元9.9至10.1之间的内部拼接。在晚期,还发现了这些早期剪接的mRNA,并且还鉴定了至少三个另外的Ad7 mRNA:1A区中的700个核苷酸长的mRNA;和1A区中的700个核苷酸长的mRNA。 1B区的1,100和核苷酸长的mRNA。在转化的大鼠细胞系中,还转录了两个早期区域1A mRNA(长950和840个核苷酸)。令人惊讶地,此外,在所有转化的细胞系中鉴定出在生产力感染的细胞中未发现的几个独特的Ad7 mRNA。它们的分子大小和编码序列在单个细胞系中有所不同。但是,这些mRNA在区域1B中具有5'末端近端部分,在区域1A中具有3'末端近端部分,这些部分通过在串联连接于转化细胞中的串联DNA序列中从区域1B延伸至区域1A转录。

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