Bavand M, Feitelson M, Laub O
Department of Genetics, Weizmann Institute of Science, Rehovot, Israel.
J Virol. 1989 Feb;63(2):1019-21. doi: 10.1128/JVI.63.2.1019-1021.1989.
We have used activity gel analysis and immunoblotting to provide evidence linking the hepatitis B virus (HBV) reverse transcriptase with its longest unassigned open reading frame (polymerase [Pol]-ORF). Activity gel analysis demonstrated that infectious HBV particles secreted by the Hep 2.2.15 cell line contain major (approximately 70 kilodaltons [kDa]) and minor (approximately 90 kDa) reverse transcriptase activities. By Western immunoblotting, we detected in both HBV particles and Hep 2.2.15 cell extract a approximately 70-kDa Pol-specific peptide. This approximately 70-kDa peptide reacted with antisera directed against the carboxy terminus of the pol gene product. No such immunoreactivity was observed with antisera against the amino terminus of the Pol peptide. The reverse transcriptase protein which was eluted from the major approximately 70-kDa region detected on an activity gel reacted with Pol-specific antisera. Furthermore, reverse transcriptase activity was immunoprecipitated from dissociated HBV particles by using Pol-specific antisera. On the basis of our results, we suggest that HBV encodes its reverse transcriptase from the Pol-ORF.
我们运用活性凝胶分析和免疫印迹法来提供证据,证明乙型肝炎病毒(HBV)逆转录酶与其最长的未指定开放阅读框(聚合酶[Pol]-ORF)之间存在联系。活性凝胶分析表明,Hep 2.2.15细胞系分泌的传染性HBV颗粒含有主要的(约70千道尔顿[kDa])和次要的(约90 kDa)逆转录酶活性。通过蛋白质免疫印迹法,我们在HBV颗粒和Hep 2.2.15细胞提取物中均检测到一种约70 kDa的Pol特异性肽。这种约70 kDa的肽与针对pol基因产物羧基末端的抗血清发生反应。而针对Pol肽氨基末端的抗血清未观察到这种免疫反应性。从活性凝胶上检测到的主要约70 kDa区域洗脱下来的逆转录酶蛋白与Pol特异性抗血清发生反应。此外,通过使用Pol特异性抗血清,从解离的HBV颗粒中免疫沉淀出了逆转录酶活性。基于我们的结果,我们认为HBV从Pol-ORF编码其逆转录酶。