Landers T A, Greenberg H B, Robinson W S
J Virol. 1977 Aug;23(2):368-76. doi: 10.1128/JVI.23.2.368-376.1977.
The circular DNA of hepatitis B Dane particles, which serves as the primer/template for an endogenous DNA polymerase, was analyzed by electrophoresis before and after a polymerase reaction and after digestion by restriction endonuclease or single-strand-specific endonuclease S1. The unreacted molecules extracted from the particles were electrophoretically heterogeneous, and treatment with S1 nuclease produced double-stranded linear DNA ranging in length from 1,700 to 2,800 base pairs (bp). After an endogenous DNA polymerase reaction, two discrete species of DNA molecules were found: a circular form and a linear form 3,200 bp long. The reaction resulted in a population of molecules with an elongated and more homogeneous double-stranded region. These results suggest that the circular molecules in Dane particles have single-stranded regions of varying lengths that are made double stranded during the DNA polymerase reaction. The endogenous DNA polymerase was found to initiate apparently at random in a region spanning more than a third of the molecule. Analysis of restriction endonuclease cleavage fragments of the fully elongated DNA revealed that although the molecules were of a uniform length, they were somewhat heterogeneous in sequence. The sum of the sizes of the 10 major endonuclease Hae III-generated fragments, detected by ethidium bromide, was 3,880 bp. Two additional fragments (B and G) detected by autoradiography after an endogenous DNA polymerase reaction with (32)P-labeled deoxynucleoside triphosphates made the total 4,910 bp.
乙肝病毒核心颗粒的环状DNA作为内源性DNA聚合酶的引物/模板,在聚合酶反应前后以及经限制性内切酶或单链特异性内切酶S1消化后进行了电泳分析。从颗粒中提取的未反应分子在电泳上具有异质性,用S1核酸酶处理产生了长度在1700至2800个碱基对(bp)之间的双链线性DNA。内源性DNA聚合酶反应后,发现了两种离散的DNA分子:一种环状形式和一种长度为3200bp的线性形式。该反应产生了一群具有伸长且更均匀双链区域的分子。这些结果表明,核心颗粒中的环状分子具有不同长度的单链区域,这些区域在DNA聚合酶反应过程中被双链化。发现内源性DNA聚合酶显然在跨越分子三分之一以上的区域随机起始。对完全伸长的DNA的限制性内切酶切割片段的分析表明,尽管分子长度一致,但它们在序列上有些异质性。通过溴化乙锭检测到的10个主要内切酶Hae III产生的片段的大小总和为3880bp。在用(32)P标记的脱氧核苷三磷酸进行内源性DNA聚合酶反应后,通过放射自显影检测到的另外两个片段(B和G)使总数达到4910bp。