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Human immunodeficiency virus reverse transcriptase base misincorporations can promote strand transfer.

机译:人类免疫缺陷病毒逆转录酶碱基误入可促进链转移。

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A system to determine if HIV-reverse transcriptase (RT) base misincorporations can promote strand transfer was constructed. A donor RNA, on which RT-directed DNA synthesis was initiated, shared homology over a 119 base internal region with an acceptor RNA, to which DNAs initiated on the donor could transfer. Products completed on the donor in the presence or absence of acceptor were isolated and PCR was used to amplify these DNAs. PCR products were ligated into a vector which had this same region (near the N-terminus of the alpha-lac gene) removed. Transformed E. coli were screened in an alpha-complementation assay by blue-white phenotype analysis with white colonies scored as those with errors in plasmid-derived alpha-lac. The frequence of white colonies +/- standard deviations was 0.031 +/- 0.006 and 0.0037 +/- 0.009, for plasmids with inserts derived from donor-directed products synthesized with 100 microM dNTPs in the presence and absence of acceptor template, respectively. Statistical analysis indicated a lower white colony frequency in the presence of acceptor (p = 0.0025). The lower frequency with acceptor implies that a portion of the errors made on the donor are transferred to the acceptor suggesting that base misincorporations can induce strand transfer.
机译:构建了一个确定 HIV 逆转录酶 (RT) 碱基错误掺入是否可以促进链转移的系统。启动RT定向DNA合成的供体RNA在119个碱基的内部区域与受体RNA共享同源性,在供体上启动的DNA可以转移到该受体上。在存在或不存在受体的情况下,分离在供体上完成的产物,并使用PCR扩增这些DNA。将PCR产物连接到一个载体中,该载体去除了相同的区域(靠近α-lac基因的N末端)。转化的大肠杆菌在α-互补试验中通过蓝白色表型分析进行筛选,白色菌落评分为质粒衍生的α-lac错误菌落。对于在存在和不存在受体模板的情况下,具有来自用 100 μM dNTP 合成的供体定向产物的插入片段的质粒,白色菌落 +/- 标准差的频率分别为 0.031 +/- 0.006 和 0.0037 +/- 0.009。统计分析表明,在受体存在的情况下,白色菌落频率较低(p = 0.0025)。受体的较低频率意味着在供体上发生的部分错误被转移到受体上,这表明碱基错误掺入可以诱导链转移。

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