Abstract
Cytoplasmic viral DNA synthesis can be followed efficiently by [3H]thymidine labeling of cells exogenously infected with Moloney murine leukemia virus. Both the negative and the positive strands of viral DNA reached their maximal level in the cytoplasm at 3.5 h postinfection. Interferon treatment before infection markedly reduced the amount of viral DNA formed during the first 3.5 h, but led to a second major wave of viral DNA synthesis, peaking at 7.5 h postinfection. No such late cytoplasmic DNA synthesis occurred in the untreated control. Inhibition of protein synthesis by cycloheximide, on the other hand, stimulated cytoplasmic viral DNA synthesis during the first 3.5 h.
| Original language | English |
|---|---|
| Pages (from-to) | 836-839 |
| Number of pages | 4 |
| Journal | Journal of Virology |
| Volume | 37 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1 Jan 1981 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- Microbiology
- Immunology
- Insect Science
- Virology
Fingerprint
Dive into the research topics of 'Cytoplasmic viral DNA synthesis in exogenous infection of murine leukemia virus: Effect of interferon and cycloheximide'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver