Seeger C, Maragos J
Department of Microbiology, Immunology and Parasitology, New York State College of Veterinary Medicine, Cornell University, Ithaca 14853-6401.
J Virol. 1990 Jan;64(1):16-23. doi: 10.1128/JVI.64.1.16-23.1990.
Replication of the woodchuck hepatitis virus (WHV) genome requires the synthesis of minus-strand DNA from an RNA template, the pregenome, by reverse transcription. During this reaction, the 5' end of minus-strand DNA becomes covalently linked to a protein. The position of the 5' end of minus-strand DNA was identified previously, but the initiation site for DNA synthesis on pregenomic RNA remained ambiguous because of a sequence repetition at the termini of the RNA template for reverse transcription. Employing a recently designed expression vector for the production of infectious WHV, we localized the origin of minus-strand DNA synthesis to the 3' end of pregenomic RNA. In addition, we identified the nucleotide sequences on pregenomic RNA that provide the signal for the initiation of reverse transcription. Removal of this signal sequence from pregenomic RNA abolished minus-strand DNA synthesis. Insertion of a DNA oligomer bearing this signal sequence at the 3' end of pregenomic RNA restored the production of minus-strand DNA joined to protein. Our results support a model in which protein is the primer for reverse transcription of minus-strand DNA of WHV.
土拨鼠肝炎病毒(WHV)基因组的复制需要通过逆转录从RNA模板(前基因组)合成负链DNA。在这个反应过程中,负链DNA的5'端与一种蛋白质形成共价连接。负链DNA的5'端位置先前已被确定,但由于逆转录RNA模板末端的序列重复,前基因组RNA上DNA合成的起始位点仍不明确。利用最近设计的用于产生传染性WHV的表达载体,我们将负链DNA合成的起始点定位到前基因组RNA的3'端。此外,我们确定了前基因组RNA上为逆转录起始提供信号的核苷酸序列。从前基因组RNA中去除该信号序列消除了负链DNA的合成。在原基因组RNA的3'端插入带有该信号序列的DNA寡聚物,恢复了与蛋白质相连的负链DNA的产生。我们的结果支持一种模型,即蛋白质是WHV负链DNA逆转录的引物。