首页> 美国卫生研究院文献>The EMBO Journal >Determination of the site of first strand transfer during Moloney murine leukemia virus reverse transcription and identification of strand transfer-associated reverse transcriptase errors.
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Determination of the site of first strand transfer during Moloney murine leukemia virus reverse transcription and identification of strand transfer-associated reverse transcriptase errors.

机译:莫洛尼氏鼠白血病病毒逆转录过程中第一链转移位点的确定以及与链转移相关的逆转录酶错误的鉴定。

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摘要

Reverse transcriptase must perform two specialized template switches during retroviral DNA synthesis. Here, we used Moloney murine leukemia virus-based vectors to examine the site of one of these switches during intracellular reverse transcription. Consistent with original models for reverse transcription, but in contrast to previous experimental data, we observed that this first strand transfer nearly always occurred precisely at the 5' end of genomic RNA. This finding allowed us to use first strand transfer to study the classes of errors that reverse transcriptase can and/or does make when it switches templates at a defined position during viral DNA synthesis. We found that errors occurred at the site of first strand transfer approximately 1000-fold more frequently than reported average reverse transcriptase error rates for template-internal positions. We then analyzed replication products of specialized vectors that were designed to test possible origins for the switch-associated errors. Our results suggest that at least some errors arose via non-templated nucleotide addition followed by mismatch extension at the point of strand transfer. We discuss the significance of our findings as they relate to the possible contribution that template switch-associated errors may make to retroviral mutation rates.
机译:逆转录酶必须在逆转录病毒DNA合成过程中执行两个专门的模板转换。在这里,我们使用基于莫洛尼鼠白血病病毒的载体来检查细胞内逆转录过程中这些开关之一的位点。与逆转录的原始模型一致,但与先前的实验数据相反,我们观察到,该第一链转移几乎总是精确地发生在基因组RNA的5'端。这一发现使我们能够利用第一链转移研究逆转录酶在病毒DNA合成过程中将模板切换到定义位置时可能和/或确实造成的错误类别。我们发现错误发生在第一条链转移的位置比模板内部位置报告的平均平均逆转录酶错误率高约1000倍。然后,我们分析了专用载体的复制产物,该产物设计用于测试与开关相关的错误的可能来源。我们的结果表明,至少一些错误是通过非模板核苷酸添加,然后在链转移点发生错配延伸而引起的。我们讨论了我们发现的意义,因为它们与模板切换相关的错误可能对逆转录病毒突变率可能产生的贡献有关。

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