Itin A, Keshet E
J Virol. 1985 Apr;54(1):236-9. doi: 10.1128/JVI.54.1.236-239.1985.
We analyzed the putative tRNA primer binding site (PBS) present in several cloned copies of the murine retrovirus-like VL30 family. In the five VL30 DNA clones analyzed, we identified PBS sequences corresponding to three different tRNA species: tRNAPro, tRNAGly, and tRNAGln. The latter two PBS sequences have not been previously encountered in other retroviral or retrovirus-like systems. A unique situation was observed in which PBS sequences complementary to two different tRNA species were flanked by otherwise identical VL30 sequences. In addition, we demonstrated the use of PBS-specific synthetic oligonucleotides for the identification of the tRNA primer and their potential utility in the direct cloning of PBS-containing DNA elements.
我们分析了鼠类逆转录病毒样VL30家族几个克隆拷贝中存在的假定tRNA引物结合位点(PBS)。在所分析的五个VL30 DNA克隆中,我们鉴定出了对应于三种不同tRNA种类的PBS序列:tRNAPro、tRNAGly和tRNAGln。后两种PBS序列在其他逆转录病毒或逆转录病毒样系统中未曾见过。我们观察到一种独特的情况,即与两种不同tRNA种类互补的PBS序列两侧是其他方面相同的VL30序列。此外,我们证明了使用PBS特异性合成寡核苷酸来鉴定tRNA引物及其在直接克隆含PBS的DNA元件中的潜在用途。