Affiliation:
1. Department of Biochemistry, Smissman Research Laboratories, University of Kansas, Lawrence, Kansas 66045
Abstract
[
3
H]RNA was synthesized in nuclei isolated at various times postinfection from the fat bodies of
Heliothis zea
larvae infected with
H. zea
nuclear polyhedrosis virus and from cultured
Spodoptera frugiperda
cells infected with
Autographa californica
nuclear polyhedrosis virus. To detect virus-specific RNA synthesis, the [
3
H]RNA was hybridized to denatured viral DNA immobilized on nitrocellulose filters. Nuclear polyhedrosis virus-specific RNA synthesis in the infected nuclei isolated from
H. zea
larval fat bodies and
S. frugiperda
cells was only inhibited 20 to 25% by concentrations of α-amanitin sufficient to inhibit the host RNA polymerase II. In addition, a productive nuclear polyhedrosis virus infection was obtained in
S. frugiperda
cells grown in the presence of an α-amanitin concentration that inhibited 90% of the cellular RNA polymerase II activity. The cellular RNA polymerase II enzyme remained sensitive to α-amanitin during infection, and there was no evidence that a virus-coded, α-amanitin-resistant enzyme was synthesized after the onset of infection. The data suggest that the bulk of nuclear polyhedrosis virus-specific RNA synthesis in isolated nuclei is transcribed by an enzyme other than the host RNA polymerase II.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
119 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献