Kulpa D, Topping R, Telesnitsky A
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109-0620, USA.
EMBO J. 1997 Feb 17;16(4):856-65. doi: 10.1093/emboj/16.4.856.
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.
逆转录酶在逆转录病毒DNA合成过程中必须进行两次特殊的模板转换。在此,我们使用基于莫洛尼鼠白血病病毒的载体来研究细胞内逆转录过程中其中一次转换的位点。与最初的逆转录模型一致,但与之前的实验数据相反,我们观察到这次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来研究逆转录酶在病毒DNA合成过程中于特定位置转换模板时可能产生和/或确实产生的错误类型。我们发现,第一链转移位点的错误发生频率比报道的模板内部位置的逆转录酶平均错误率高出约1000倍。然后,我们分析了专门设计用于测试转换相关错误可能来源的载体的复制产物。我们的结果表明,至少一些错误是通过非模板化核苷酸添加,然后在链转移点进行错配延伸而产生的。我们讨论了我们的发现的意义,因为它们与模板转换相关错误可能对逆转录病毒突变率产生的潜在贡献有关。