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PMID: 1373117 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Antisense CCAAT/enhancer-binding protein RNA suppresses coordinate gene expression and triglyceride accumulation during differentiation of 3T3-L1 preadipocytes.

Genes & development ·Vol. 6 ·No. 4 ·1992-04-00 ·Pages 533-44

Lin FT, Lane MD

Abstract

Previous studies suggest that the CCAAT/enhancer-binding protein (C/EBP) functions in the coordinate expression of adipocyte genes during differentiation of 3T3-L1 preadipocytes. We sought to block expression of C/EBP selectively using a bovine papilloma virus (BPV) vector to direct transcription of a approximately 0.4-kb segment of C/EBP cDNA (in antisense orientation) containing translated sequence 5' to that encoding the basic and leucine zipper regions of the protein. Vector-directed expression of antisense C/EBP RNA in 3T3-L1 preadipocytes inhibited expression of C/EBP mRNA and protein, as well as several adipose-specific mRNAs, and also prevented cytoplasmic triglyceride accumulation. Rescue of the "adipocyte phenotype" was accomplished by transfection of cells expressing antisense RNA with a modified BPV vector that directs transcription of the complementary sense C/EBP RNA.

MeSH Terms
3T3 Cells Adipose Tissue/cytology,metabolism Animals Blotting, Southern Blotting, Western CCAAT-Enhancer-Binding Proteins Cell Differentiation DNA/genetics DNA-Binding Proteins/genetics Gene Expression Genetic Vectors Leucine Zippers/genetics Mice Nuclear Proteins/genetics RNA/genetics Transcription, Genetic Transfection Triglycerides/metabolism
Chemicals
CCAAT-Enhancer-Binding Proteins DNA-Binding Proteins Nuclear Proteins Triglycerides RNA DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lin F T
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Lane M D
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
1992-04-00
Pages
533-44
Language
English
Region
United States
NLM ID
8711660
Subset
IM
Grants
NIDDK NIH HHS · NIDDK-38418 · United States
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