» Articles » PMID: 7218436

Adenovirus Type 2 Expresses Fiber in Monkey-human Hybrids and Reconstructed Cells

Overview
Journal J Virol
Date 1981 Feb 1
PMID 7218436
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Adenovirus type 2 protein expression was measured by indirect immunofluorescence in monkey-human hybrids and in cells reconstructed from monkey and human cell karyoplasts and cytoplasts. Monkey-human hybrid clones infected with adenovirus type 2 expressed fiber protein, whereas infected monkey cells alone did not. Hybrids constructed after the parental monkey cells were infected with adenovirus type 2 demonstrated that fiber synthesis in these cells could be rescued by fusion to uninfected human cells. Thus, human cells contain a dominant factor that acts in trans and overcomes the inability of monkey cells to synthesize fiber. Cells reconstructed from infected human karyoplasts and monkey cytoplasts expressed fiber, whereas cells reconstructed from infected monkey karyoplasts and human cytoplasts did not. These results are consistent with the hypothesis that the block to adenovirus replication in monkey cells involves a nuclear event that prevents the formation of functional mRNA for some late viral proteins including fiber polypeptide. Furthermore, they suggest that the translational apparatus of monkey cells is competent to translate functional fiber mRNA synthesized in human cells.

Citing Articles

Normal translation of human adenovirus mRNA in cell-free lysates prepared from abortively as well as productively infected monkey cells.

Quinlan M, Klessig D J Virol. 1982; 44(1):426-30.

PMID: 7143572 PMC: 256279. DOI: 10.1128/JVI.44.1.426-430.1982.


Translation of adenovirus 2 late mRNAs microinjected into cultured African green monkey kidney cells.

Richardson W, Anderson C J Virol. 1984; 51(2):559-62.

PMID: 6748164 PMC: 254474. DOI: 10.1128/JVI.51.2.559-562.1984.


Identification of key regulated events early in the life of hybrid animal cells constructed by nuclear transplantation.

Hightower M, Bruno J, Lucas J Proc Natl Acad Sci U S A. 1983; 80(17):5310-4.

PMID: 6577429 PMC: 384245. DOI: 10.1073/pnas.80.17.5310.


Aberrant distribution of human adenovirus type 2 late proteins in monkey kidney cells.

Cepko C, Sharp P J Virol. 1983; 46(1):302-6.

PMID: 6402607 PMC: 255123. DOI: 10.1128/JVI.46.1.302-306.1983.


Altered mRNA splicing in monkey cells abortively infected with human adenovirus may be responsible for inefficient synthesis of the virion fiber polypeptide.

Anderson K, Klessig D Proc Natl Acad Sci U S A. 1984; 81(13):4023-7.

PMID: 6330731 PMC: 345360. DOI: 10.1073/pnas.81.13.4023.


References
1.
Feldman L, Butel J, Rapp F . Interaction of a simian papovavirus and adenoviruses. I. Induction of adenovirus tumor antigen during abortive infection of simian cells. J Bacteriol. 1966; 91(2):813-8. PMC: 314934. DOI: 10.1128/jb.91.2.813-818.1966. View

2.
Reich P, Baum S, Rose J, Rowe W, Weissman S . Nucleic acid homology studies of adenovirus type 7-SV40 interactions. Proc Natl Acad Sci U S A. 1966; 55(2):336-41. PMC: 224145. DOI: 10.1073/pnas.55.2.336. View

3.
Pettersson U, Philipson L, Hoglund S . Structural proteins of adenoviruses. I. Purification and characterization of the adenovirus type 2 hexon antigen. Virology. 1967; 33(4):575-90. DOI: 10.1016/0042-6822(67)90057-8. View

4.
Baum S, Wiese W, Reich P . Studies on the mechanism of enhancement of adenovirus 7 infection in African green monkey cells by simian virus 40: formation of adenovirus-specific RNA. Virology. 1968; 34(2):373-6. DOI: 10.1016/0042-6822(68)90253-5. View

5.
Thomas D, Green M . Biochemical studies on adenovirus multiplication. XV. Transcription of the adenovirus type II genome during productive infection. Virology. 1969; 39(2):205-10. DOI: 10.1016/0042-6822(69)90040-3. View