Wong M L, Hsu M T
Department of Microbiology, Mount Sinai Medical Center, New York, New York 10029.
J Virol. 1988 Apr;62(4):1227-34. doi: 10.1128/JVI.62.4.1227-1234.1988.
We used the psoralen-cross-linking technique to investigate the structures of adenovirus nucleoprotein complexes during infection. At late times after infection, three types of psoralen cross-linking patterns were observed. A high cross-linking pattern (type I), with about one cross-link in every 10 to 17 base pairs, was found for the newly synthesized and the bulk of the adenovirus late chromatin. Viral templates involved in replication, transcription, and recombination were all found to exhibit this cross-linking pattern. These results suggest that there is no nucleosome-like organization in the unpackaged late adenovirus nucleoprotein complexes. The second type of cross-linking pattern (type II) had a low cross-linking density of about one cross-link in every 700 to 1,000 base pairs. This cross-linking pattern was found to be associated with the viral DNA in the mature virus particles. The sequences at the termini of the virion DNAs, however, were found to have higher cross-linking densities, as shown by electron microscopy. The third type of cross-linking pattern (type III) was composed of a mixture of various proportions of type I and type II patterns in a single molecule. This mixed cross-linking pattern suggests that these molecules are virion assembly intermediates, with viral DNA being partially packaged in the virus particles. The organization of adenovirus nucleoprotein complexes at early times after infection was analyzed by the gel electrophoresis technique following digestion of the DNA with a restriction enzyme that was inhibited by cross-links. Our data suggest that the viral nucleoprotein complexes at early times after infection have accessibility to psoralen cross-linking between the virion DNA and the late viral nucleoprotein complexes. The observed cross-linking density of the early nucleoprotein complex DNA, however, was inconsistent with the nucleosomelike organization suggested by previous investigators.
我们使用补骨脂素交联技术来研究腺病毒感染期间核蛋白复合物的结构。在感染后的晚期,观察到三种类型的补骨脂素交联模式。对于新合成的以及大部分腺病毒晚期染色质,发现了一种高交联模式(I型),每10至17个碱基对中约有一个交联。参与复制、转录和重组的病毒模板均显示出这种交联模式。这些结果表明,未包装的晚期腺病毒核蛋白复合物中不存在核小体样组织。第二种交联模式(II型)的交联密度较低,每700至1000个碱基对中约有一个交联。这种交联模式与成熟病毒颗粒中的病毒DNA相关。然而,如电子显微镜所示,病毒粒子DNA末端的序列具有更高的交联密度。第三种交联模式(III型)由单个分子中不同比例的I型和II型模式混合组成。这种混合交联模式表明这些分子是病毒粒子组装中间体,病毒DNA部分包装在病毒粒子中。在感染后早期,通过用受交联抑制的限制性内切酶消化DNA后的凝胶电泳技术分析腺病毒核蛋白复合物的组织。我们的数据表明,感染后早期的病毒核蛋白复合物可进行补骨脂素在病毒粒子DNA与晚期病毒核蛋白复合物之间的交联。然而,观察到的早期核蛋白复合物DNA的交联密度与先前研究者提出