Literature DB >> 2157885

Orthopoxvirus gene expression in Xenopus laevis oocytes: a component of the virion is needed for late gene expression.

R F Massung1, R W Moyer.   

Abstract

We have examined the feasibility of using Xenopus laevis oocytes microinjected with rabbit poxvirus as a system to study poxvirus gene expression. The injection of either intact virus or subviral cores resulted in accurate synthesis of viral proteins. This expression was dependent on the multiplicity of injected virus, with the optimal injected dose being equivalent to approximately 300 PFU per oocyte. Extensive viral gene expression including late viral protein synthesis was observed when intact virions were microinjected into the oocyte. However, the injection of subviral cores resulted in only early protein synthesis. When oocytes were injected with a mixture of subviral cores and the nonionic detergent-soluble fraction was removed from virus during the preparation of cores, both early and late viral proteins were synthesized. Therefore, the detergent-soluble fraction appears to contain a factor(s) required for the transition from early to late gene expression.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2157885      PMCID: PMC249389          DOI: 10.1128/JVI.64.5.2280-2289.1990

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  40 in total

1.  THE CYCLE OF MULTIPLICATION OF VACCINIA VIRUS IN EARLE'S STRAIN L CELLS. I. UPTAKE AND PENETRATION.

Authors:  S DALES; R KAJIOKA
Journal:  Virology       Date:  1964-11       Impact factor: 3.616

2.  Eukaryotic transient expression system dependent on transcription factors and regulatory DNA sequences of vaccinia virus.

Authors:  M A Cochran; M Mackett; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

3.  Polyadenylate polymerase from vaccinia virions.

Authors:  B Moss; E N Rosenblum; E Paoletti
Journal:  Nat New Biol       Date:  1973-09-12

4.  RNA polymerase activity in purified infectious vaccinia virus.

Authors:  W Munyon; E Paoletti; J T Grace
Journal:  Proc Natl Acad Sci U S A       Date:  1967-12       Impact factor: 11.205

Review 5.  Biology of poxviruses.

Authors:  S Dales; B G Pogo
Journal:  Virol Monogr       Date:  1981

6.  Controlled degradation of vaccinia virions in vitro: an electron microscopic study.

Authors:  K B Easterbrook
Journal:  J Ultrastruct Res       Date:  1966-03

7.  A soluble transcription system derived from purified vaccinia virions.

Authors:  F Golini; J R Kates
Journal:  J Virol       Date:  1985-01       Impact factor: 5.103

8.  Vaccinia virus structural polypeptide derived from a high-molecular-weight precursor: formation and integration into virus particles.

Authors:  E Katz; B Moss
Journal:  J Virol       Date:  1970-12       Impact factor: 5.103

9.  Formation of a vaccinia virus structural polypeptide from a higher molecular weight precursor: inhibition by rifampicin.

Authors:  E Katz; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1970-07       Impact factor: 11.205

10.  Selective transcription of vaccinia virus genes in template dependent soluble extracts of infected cells.

Authors:  C Puckett; B Moss
Journal:  Cell       Date:  1983-12       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.