Document Detail


Extinction of JC virus tumor-antigen expression in glial cell--fibroblast hybrids.
MedLine Citation:
PMID:  2845416     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
JC virus (JCV) is a ubiquitous human papovavirus that shares sequence and structural homology with simian virus 40 (SV40). In contrast to SV40, expression of JCV is restricted to a small number of cell types, including human fetal glial cells, uroepithelial cells, amnion cells, and some endothelial cells. To study the control of JCV early region expression, we made heterokaryons and stable hybrids between JCV-transformed hamster glial cells and mouse fibroblasts. Binucleate heterokaryons exhibited extinction of large tumor antigen expression in the hamster nuclei as assayed by indirect immunofluorescence. This extinction was both time and dose dependent: extinction reached maximal levels at 24-36 hr after fusion and was dependent on the ratio of glial cell to fibroblast nuclei in multinucleated heterokaryons. Extinction also was observed in stable hybrids between the glial cells and mouse Ltk- cells. Southern blot analysis showed that the extinguished hybrids contained viral sequences. Reexpression of large tumor antigen was observed in several subclones, suggesting that extinction was correlated with the loss of murine fibroblast chromosomes from these hybrids. The cis-acting region that mediates extinction resides within the viral regulatory region, which contains two 98-base-pair repeats that have enhancer activity. These data demonstrate that cellular factors that negatively regulate viral gene expression contribute to the restricted cell-type specificity of this virus.
Authors:
A H Beggs; R J Frisque; G A Scangos
Related Documents :
3970696 - Effect of monensin on myoblast fusion.
18600676 - A production of monoclonal antibodies by a simple electrofusion technique induced by ac...
8991086 - Cell fusion during yeast mating requires high levels of a-factor mating pheromone.
18981126 - Processing of an antigenic sequence from igg constant domains for presentation by mhc c...
12543976 - The cellular and molecular origins of beak morphology.
22212726 - A cell-contact-regulated operon is involved in genetic variability in neisseria meningi...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  85     ISSN:  0027-8424     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  1988 Oct 
Date Detail:
Created Date:  1988-11-21     Completed Date:  1988-11-21     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  7632-6     Citation Subset:  IM    
Affiliation:
Department of Biology, Johns Hopkins University, Baltimore, MD 21218.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, Viral, Tumor / biosynthesis,  genetics*
Blotting, Southern
Cell Fusion
Cell Line
Cricetinae
DNA / analysis
Fibroblasts
Fluorescent Antibody Technique
Gene Expression Regulation*
Glioma / microbiology*
Humans
Hybrid Cells / microbiology*
JC Virus / genetics*,  immunology
Mice
Polyomavirus / genetics*
Tumor Cells, Cultured
Grant Support
ID/Acronym/Agency:
CA 38789/CA/NCI NIH HHS; CA 40572/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Antigens, Viral, Tumor; 9007-49-2/DNA
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Evidence for the loop model of signal-sequence insertion into the endoplasmic reticulum.
Next Document:  Cloning and characterization of a cDNA encoding the chloroplastic copper/zinc-superoxide dismutase f...