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Nucleotide sequences of a feline leukemia virus subgroup A envelope gene and long terminal repeat and evidence for the recombinational origin of subgroup B viruses.

机译:猫白血病病毒亚组A包膜基因的核苷酸序列和长末端重复序列以及B亚组病毒重组来源的证据。

摘要

Molecular clones of the subgroup A feline leukemia virus FeLV-A/Glasgow-1 have been obtained. Nucleotide sequence analysis of the 3' end of the proviral genome and comparison with the published sequence of FeLV-B/Gardner-Arnstein showed that the most extensive differences are located within the 5' domain of the env gene. Within this domain, several divergent regions of env are separated by more conserved segments. The 3' end of env is highly conserved, with only a single amino acid coding difference in p15env. The proviral long terminal repeats are also highly conserved, differing by only eight base substitutions and one base insertion. Specific probes constructed from the FeLV-A or FeLV-B env genes were used to compare the env genes of various exogenous FeLV isolates and the endogenous FeLV-related proviruses of normal cat DNA. An FeLV-A-derived env probe showed no hybridization to normal cat DNA but detected all FeLV-A and FeLV-C isolates tested. In contrast, an FeLV-B env probe detected independent FeLV-B isolates and a family of endogenous FeLV-related proviruses. Our observations provide strong evidence to support the hypothesis that FeLV-B viruses have arisen by recombination between FeLV-A and endogenous proviral elements in cat DNA.
机译:已经获得了亚类猫白血病病毒FeLV-A / Glasgow-1的分子克隆。前病毒基因组3'末端的核苷酸序列分析以及与已发表的FeLV-B / Gardner-Arnstein序列的比较表明,最广泛的差异位于env基因的5'域内。在该域内,env的几个不同区域被更保守的片段隔开。 env的3'端高度保守,p15env中只有一个氨基酸编码差异。前病毒的长末端重复序列也是高度保守的,区别仅在于八个碱基取代和一个碱基插入。由FeLV-A或FeLV-B env基因构建的特异性探针用于比较各种外源FeLV分离株的env基因和正常猫DNA的内源FeLV相关原病毒。 FeLV-A衍生的env探针未显示与正常猫DNA的杂交,但检测到所有测试的FeLV-A和FeLV-C分离株。相反,FeLV-B env探针检测到独立的FeLV-B分离株和内源性FeLV相关的原病毒家族。我们的观察结果提供了有力的证据来支持FeLV-B病毒是通过猫猫DNA中的FeLV-A与内源性前病毒成分重组产生的假说的。

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  • 作者

    Warnock Mary;

  • 作者单位
  • 年度 1986
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
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