Abstract
We have cloned the upstream region of the rat phospholipase C-gamma 1 gene and characterized its promoter activity. The 5'-upstream sequence is highly rich in GC, enriched with CpG dinucleotides and lacks a TATA motif. This sequence also contains many putative binding sites for regulatory proteins. Primer extension and RNase protection assay demonstrated a single transcriptional start site located at 103 nucleotides upstream of the ATG start codon. The transcriptional activities of various 5'-deleted fragments, fused with chloramphenicol acetyltransferase gene, were examined after transfection into C2C12 myoblast. Multiple positive and negative regulatory sites were observed.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Base Sequence
-
Blotting, Southern
-
Brain / enzymology
-
Cell Line
-
Chloramphenicol O-Acetyltransferase / genetics
-
Chloramphenicol O-Acetyltransferase / metabolism
-
Cloning, Molecular
-
DNA
-
Genomic Library
-
Isoenzymes / genetics*
-
Isoenzymes / metabolism
-
Mice
-
Molecular Sequence Data
-
Oligodeoxyribonucleotides
-
Phosphatidylinositol Diacylglycerol-Lyase
-
Phosphoric Diester Hydrolases / genetics*
-
Phosphoric Diester Hydrolases / metabolism
-
Promoter Regions, Genetic*
-
Rats
-
Recombinant Proteins / metabolism
-
Restriction Mapping
-
Transcription, Genetic
-
Transfection
Substances
-
Isoenzymes
-
Oligodeoxyribonucleotides
-
Recombinant Proteins
-
DNA
-
Chloramphenicol O-Acetyltransferase
-
Phosphoric Diester Hydrolases
-
Phosphatidylinositol Diacylglycerol-Lyase
Associated data
-
GENBANK/L14476
-
GENBANK/L16870
-
GENBANK/L16871
-
GENBANK/L16872
-
GENBANK/L16873
-
GENBANK/L16874
-
GENBANK/L16875
-
GENBANK/L16876
-
GENBANK/L16877
-
GENBANK/L16878