1982
DOI: 10.1007/978-3-642-68318-3_4
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Regulation of Adenovirus Gene Expression

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1982
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Cited by 20 publications
(10 citation statements)
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“…The results obtained when the antiserum to the 72-kd protein (the viral E2 gene product) was used clearly show that early gene expression could be detected in the high-multiplicity hr-1 infection (Fig. 4B); thus, there must also have been expression of the 12S EtA RNA in these cells, as has been shown previously (3,37). Therefore, the ElA peptide serum detects only the 13S products which were absent from the hr-1 infection.…”
supporting
confidence: 67%
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“…The results obtained when the antiserum to the 72-kd protein (the viral E2 gene product) was used clearly show that early gene expression could be detected in the high-multiplicity hr-1 infection (Fig. 4B); thus, there must also have been expression of the 12S EtA RNA in these cells, as has been shown previously (3,37). Therefore, the ElA peptide serum detects only the 13S products which were absent from the hr-1 infection.…”
supporting
confidence: 67%
“…The use of appropriate viral systems affords the opportunity to overcome these limitations. The expression of adenovirus genes during the early phase of a viral infection is strictly regulated at multiple levels of RNA biogenesis (33,37,50). Much of the regulation of early viral gene expression occurs at the level of transcription and is mediated through the action of specific viral gene products (32,34,35).…”
mentioning
confidence: 99%
“…The human adenovirus (adeno), type 2 genome has seven transcription units that are expressed early after infection, the L1, Ela, Elb, E2a, E2b, E3, and E4 regions (1). Of these the E3 region codes for a Mr 19,000 protein (2).…”
mentioning
confidence: 99%
“…However, as the E2 and E3 transcription units do not hybridize a human probe, there must be something particular about E1A, E1B, and E4, which do allow hybridization. The only major difference in the transcriptional regulation between El A, E1B, and E4 on the one hand and E2 and E3 on the other, is the change in promoter sites utilized between early and intermediate expression (Chow et ai, 1979) for the E2 and E3 genes (see Persson and Philipson, 1982, for a review). Once the exact sequences involved in the hybridization of Ad2 and human DNA have been identified the differences between these two classes of genes might be clearer.…”
Section: Discussionmentioning
confidence: 99%