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Cited by 240

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Autoregulation of simian virus 40 gene A by T antigen.

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Reed, S I, Stark, G R, Alwine, J C·1976·Proceedings of the National Academy of Sciences

Abstract

During lytic infection by simian virus 40, gene A is transcribed into early RNA, which is translated into A protein (T antigen). Both the rate of synthesis and the intracellular amount of early RNA are higher in cells infected by temperature-sensitive A (tsA) mutants than in cells infected by wild-type virus. These differences are observed at permissive temperature (32 degrees) and are amplified greatly after a shift to restrictive temperature (41 degrees). For example, at 32 degrees cells infected by tsA mutants synthesize early RNA approximately twice as fast as cells infected by wild-type virus. After the shift to 41 degrees, the rate of synthesis in the tsA infection increases to 15 times the rate in the wild-type infection. In contrast, cells infected by tsA mutants do not overproduce late RNA. We suggest that the A protein regulates its own synthesis by negative feedback control of gene A transcription.

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Metadata

Authors
Reed, S. I., Stark, G. R., & Alwine, J. C.
Venue
Proceedings of the National Academy of Sciences
Published
1976-09
Volume
73
Issue
9
Pages
3083-3087
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2081938019
Cited by
240
References
0
FWCI
13.76
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Autoregulation of simian virus 40 gene A by T antigen. https://app.cochat.ai/papers/10.1073/pnas.73.9.3083
The paper
Reed, S. I., Stark, G. R., & Alwine, J. C. (1976). Autoregulation of simian virus 40 gene A by T antigen. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.73.9.3083

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.