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PMID: 7541561 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Endogenous and transfected mouse alpha-fetoprotein genes in undifferentiated F9 cells are activated in transient heterokaryons.

Somatic cell and molecular genetics ·Vol. 21 ·No. 1 ·1995-01-00 ·Pages 19-31

Spear BT, Ellis AW

Abstract

Mouse F9 teratocarcinoma cells provide a system to study developmentally regulated alpha-fetoprotein (AFP) gene expression. AFP is not expressed in undifferentiated F9 cells but is induced when cells differentiate as cell aggregates in the presence of retinoic acid. Previous studies have led to the suggestion that undifferentiated F9 cells contain negative regulators of AFP expression. To test this, we have used transient heterokaryons to ask whether inactive AFP genes in undifferentiated F9 cells are responsive to positively acting trans-acting factors. Our results indicate that silent endogenous and transfected AFP genes are activated when undifferentiated F9 cells are fused to human hepatoma HepG2 cells. This suggests that the lack of AFP expression in undifferentiated F9 cells is due to the absence or insufficient level of positive-acting transcription factors, rather than the presence of dominant negative regulators. We also demonstrate that stably transfected AFP genes, although unmethylated, are properly regulated in F9 cells.

MeSH Terms
Animals Cell Differentiation Cell Fusion Cell Line Cell Nucleus/genetics,metabolism Gene Expression Regulation, Developmental Gene Expression Regulation, Neoplastic Gene Transfer Techniques Male Mice Teratocarcinoma/genetics,metabolism,pathology alpha-Fetoproteins/biosynthesis,genetics
Chemicals
alpha-Fetoproteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Spear B T
Department of Microbiology & Immunology, University of Kentucky College of Medicine, Lexington 40536-0084, USA.
Ellis A W
Article Info
Journal
Somatic cell and molecular genetics
Abbr.
Somat Cell Mol Genet
ISSN
0740-7750
Published
1995-01-00
Pages
19-31
Language
English
Region
United States
NLM ID
8403568
Subset
IM
Grants
NIGMS NIH HHS · GM-45253 · United States
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