Sites of transcription of adenovirus type 5 genomes in relation to early viral DNA replication in infected HeLa cells. A high resolution in situ hybridization and autoradiographical study
Sites of transcription of adenovirus type 5 genomes in relation to early viral DNA replication in infected HeLa cells. A high resolution in situ hybridization and autoradiographical study
复制标题
5 型腺病毒基因组的转录位点与受感染 HeLa 细胞中早期病毒 DNA 复制相关。
DOI:
10.1016/0248-4900(91)90060-z
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发表时间:
1991
影响因子:
2.7
通讯作者:
E. Puvion
中科院分区:
文献类型:
--
作者:
F. Puvion;E. Puvion
The distribution of viral RNA molecules in HeLa cells infected with adenovirus type 5 (Ad5) was determined byin situhybridization at the ultrastructural level at an intermediate stage of nuclear transformation, when viral DNA synthetic activities were maximal but progeny viruses were still sparse. Transcription sites of the viral DNA were localized by short pulse, high resolution autoradiography. Nascent viral RNA was found mainly within the nuclear compartment identified at the peripheral replicative zone, which is known to be the main replicative site of Ad5 viral genomes. Viral RNA molecules also were present, but to a markedly lesser extent, within the contiguous single‐stranded (ss) DNA accumulation site, another intranuclear virus‐induced structure in which some replication of viral genomes also occurs. Two other virus‐induced nuclear structures contained viral RNA, the occasional exceptionally enlarged clusters of interchromatin granules and the compact rings, both DNA‐free structures of unknown significance but which might play a role in the process of maturation of the Ad5 primary transcripts. Viral messenger RNA molecules were localized over the large areas of the cytoplasm which contain numerous ribosomes. Our analysis of the effects of various enzymatic pretreatments of the sections of infected cells on the revelation of nascent RNA byin situhybridization is reviewed.
影响因子:
3.7
作者:
Bodnar,JW;Pearson,GD
通讯作者:
Pearson,GD
DOI:
--
发表时间:
1986
期刊:
Cancer surveys
影响因子:
--
作者:
Berk,AJ
通讯作者:
Berk,AJ