Abstract:
:By pretreating simian virus 40-infected BSC-1 cells with glucosamine, [(3)H]uridine labeling of both cellular and viral RNA can be halted instantaneously by addition of cold uridine. We have studied the fate of pulse-labeled viral RNA from cells at 45 h postinfection under these conditions. During a 5-min period of labeling, both the messenger and nonmessenger regions of the late strand were transcribed. After various chase periods, nuclear viral species which sediment at 19, 17.5, and 16S were observed. Nuclear viral RNA decays in a multiphasic manner. Of the material present at the beginning of the chase period, 50% was degraded rapidly with a half-life of 8 min (initial processing). This rapidly degraded material was that fraction of the late strand which did not give rise to stable late mRNA species. Forty percent was transported to the cytoplasm, and 10% remained in the nucleus as material which sedimented in the 2 to 4S region. These 2 to 4S viral RNAs had a half-life of 3 h, and hybridization studies suggest that they are in part coded for by the late-strand nonmessenger region and are derived from the initial nuclear processing step. Another part is coded for by the late-strand messenger region and may be generated by some subsequent nuclear cleavages of 19S RNA into 17.5 and 16S RNAs. Transport of nuclear viral RNA into the cytoplasm was detected after a 5-min pulse and a 7-min chase. The maximum amount of labeled viral RNA was accumulated in the cytoplasm after a 30-min to 1-h chase. At least two viral cytoplasmic species were observed. Kinetic data suggest that 19S RNA is transported directly from the nucleus. Whether cytoplasmic 16S is formed by cleavage of 19S RNA in the cytoplasm is not clear. The half-lives of cytoplasmic 19 and 16S RNAs can be approximated as 2 and 5 h, respectively.
journal_name
J Viroljournal_title
Journal of virologyauthors
Chiu NH,Radonovich MF,Thoren MM,Salzman NPdoi
10.1128/JVI.28.2.590-599.1978subject
Has Abstractpub_date
1978-11-01 00:00:00pages
590-9issue
2eissn
0022-538Xissn
1098-5514journal_volume
28pub_type
杂志文章abstract::Differential effect of various metabolic inhibitors on the development of hemadsorption activity and virus formation in cells infected with Newcastle disease virus (NDV) was investigated. It was found that, in BHK-21 cells infected with NDV, cycloheximide did not prevent the development of hemadsorption activity, wher...
journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.11.4.479-486.1973
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pub_type: 杂志文章
doi:10.1128/JVI.53.3.966-968.1985
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abstract::The mammalian tripartite motif protein, TRIM5α, recognizes retroviral capsids entering the cytoplasm and blocks virus infection. Depending on the particular TRIM5α protein and retrovirus, complete disruption of the TRIM5α RING domain decreases virus-restricting activity to various degrees. TRIM5α exhibits RING domain-...
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doi:10.1128/JVI.52.2.448-456.1984
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pub_type: 杂志文章
doi:10.1128/JVI.67.12.7181-7189.1993
更新日期:1993-12-01 00:00:00
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doi:10.1128/JVI.15.3.534-539.1975
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journal_title:Journal of virology
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doi:10.1128/JVI.16.6.1608-1614.1975
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doi:10.1128/JVI.65.8.3973-3985.1991
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journal_title:Journal of virology
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doi:10.1128/JVI.64.1.322-330.1990
更新日期:1990-01-01 00:00:00
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journal_title:Journal of virology
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doi:10.1128/JVI.64.9.4115-4122.1990
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journal_title:Journal of virology
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更新日期:1989-04-01 00:00:00
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更新日期:1992-06-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:1998-06-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:1983-01-01 00:00:00
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更新日期:2002-06-01 00:00:00