Department of Biochemistry and Biophysics and Center for RNA Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
Nat Struct Mol Biol. 2010 Jan;17(1):83-9. doi: 10.1038/nsmb.1687. Epub 2009 Dec 6.
We identified a sequence embedded in the U3-R region of HIV-1 RNA that is highly complementary to human tRNA(3)(Lys). The free energy of annealing to tRNA(3)(Lys) is significantly lower for this sequence and the primer-binding site than for other viral sequences of similar length. The only interruption in complementarity is a 29-nucleotide segment inserted where a tRNA intron would be expected. The insert contains the TATA box for viral RNA transcription. The embedded sequence includes a 9-nucleotide segment previously reported to aid minus-strand transfer by binding the primer tRNA(3)(Lys). Reconstituting transfer in vitro, we show that including segments from the embedded sequence in the acceptor template, beyond the 9 nucleotides, further increases transfer efficiency. We propose that a gene encoding tRNA(3)(Lys) was incorporated during HIV-1 evolution and retained, largely intact, because of its roles in transcription and strand transfer.
我们鉴定了 HIV-1 RNA 的 U3-R 区中一个高度互补于人类 tRNA(3)(Lys)的序列。与其他类似长度的病毒序列相比,该序列和引物结合位点与 tRNA(3)(Lys)退火的自由能明显更低。唯一的不互补性中断是在预期插入 tRNA 内含子的位置插入了 29 个核苷酸片段。该插入物包含病毒 RNA 转录的 TATA 盒。嵌入序列包含一个 9 个核苷酸的片段,先前的研究表明该片段通过结合引物 tRNA(3)(Lys)有助于负链转移。我们在体外重建转移实验,结果表明在接受模板中,除了 9 个核苷酸之外,包含来自嵌入序列的片段可以进一步提高转移效率。我们提出,在 HIV-1 进化过程中整合了编码 tRNA(3)(Lys)的基因,并由于其在转录和链转移中的作用而得以保留,基本上完整无损。