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腺病毒DNA合成与病毒组装相关联。

Adenovirus DNA synthesis is coupled to virus assembly.

作者信息

Weber J M, Déry C V, Mirza M A, Horvath J

出版信息

Virology. 1985 Jan 30;140(2):351-9. doi: 10.1016/0042-6822(85)90371-x.

Abstract

The relationship between viral DNA synthesis and virion assembly was studied in adenovirus type 2 infected HEp2 cells. When cells were infected at the restrictive temperature with ts3, an assembly-negative mutant which permits normal viral DNA and protein synthesis, labeled and shifted to the permissive temperature, only de novo synthesized nonradioactive viral DNA was encapsidated. This suggested that only concurrently synthesized DNA is encapsidated. Blocking protein or DNA synthesis with cycloheximide or hydroxyurea after the temperature shift inhibited virus assembly. Therefore efficient virus assembly requires both concurrent protein and DNA synthesis. When DNA synthesis was arrested by shifting ts125 infected cells to the restrictive temperature, protein synthesis continued but assembly was completely blocked. Sucrose gradient sedimentation analysis of nuclear extracts of wt and ts3 infected cells provided evidence in support of a physical coupling between replication complexes and virus assembly complexes. Further evidence of coupling was also shown by preferential pulse labeling of the molecular right end of the genome isolated from reversibly cross-linked assembly intermediate particles. While DNA replication is not dependent on concurrent virion assembly, at least some significant proportion of replication complexes appear to be coupled to and are prerequisite for virion assembly.

摘要

在腺病毒2型感染的HEp2细胞中研究了病毒DNA合成与病毒体装配之间的关系。当细胞在限制温度下用ts3(一种允许正常病毒DNA和蛋白质合成的装配阴性突变体)感染、标记后转移到允许温度时,只有新合成的非放射性病毒DNA被包装。这表明只有同时合成的DNA才会被包装。温度转移后用环己酰亚胺或羟基脲阻断蛋白质或DNA合成会抑制病毒装配。因此,高效的病毒装配需要同时进行蛋白质和DNA合成。当通过将ts125感染的细胞转移到限制温度来阻止DNA合成时,蛋白质合成继续,但装配完全受阻。对野生型和ts3感染细胞的核提取物进行蔗糖梯度沉降分析,为复制复合物与病毒装配复合物之间的物理偶联提供了证据。从可逆交联的装配中间颗粒中分离出的基因组分子右端的优先脉冲标记也显示了偶联的进一步证据。虽然DNA复制不依赖于同时进行的病毒体装配,但至少有相当一部分复制复合物似乎与病毒体装配偶联,并且是病毒体装配的先决条件。

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