GSBS Student Publications

Title

Positive- and negative-acting promoter sequences regulate cell type-specific expression of the rat synapsin I gene

GSBS Program

Biochemistry & Molecular Pharmacology

UMMS Affiliation

Graduate School of Biomedical Sciences; Department of Neurology

Date

10-11-1991

Document Type

Article

Medical Subject Headings

Animals; Base Sequence; Brain; Cell Line; Chloramphenicol O-Acetyltransferase; *Gene Expression Regulation; Hela Cells; Humans; Liver; Molecular Sequence Data; Oligodeoxyribonucleotides; PC12 Cells; Plasmids; *Promoter Regions (Genetics); RNA, Messenger; Recombinant Fusion Proteins; Synapsins; Transfection

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

The phosphoprotein synapsin I is expressed exclusively in neuronal cells. We are interested in elucidating the promoter sequences involved in cell type-specific expression of the synapsin I gene. The PC12 cell line expresses the 3.4 kb and 4.5 kb synapsin I mRNAs and is used to analyze cell type-specific gene expression. A series of deletion fragments of the rat synapsin I gene promoter were fused to the promoterless reporter gene encoding bacterial chloramphenicol acetyltransferase (CAT) for transfection analysis in PC12 cells and in HeLa cells, which do not express the gene. A -349 bp to +110 bp rat synapsin I promoter fragment contains a positive regulator, shown to be 33-times more active in PC12 cells than HeLa cells. Transfection of reporter plasmids containing up to 4.4 kb of rat synapsin I gene promoter sequences exhibit significantly reduced CAT activity in PC12 cells. The reduction in CAT expression was attributed to a negative regulator located between -349 bp and -1341 bp in the rat synapsin I promoter. Our results suggest that both positive and negative-acting sequence elements regulate cell type-specific expression of the rat synapsin I gene.

Rights and Permissions

Citation: Brain Res Mol Brain Res. 1991 Oct;11(3-4):345-53.

Related Resources

Link to article in PubMed

Journal Title

Brain research. Molecular brain research

PubMed ID

1661826