Abstract
The rat myosin light chain (MLC)1/3 gene locus contains a potent muscle-specific enhancer, located downstream of the coding region, greater than 24 kilobases away from the MLC1 transcription start site. To assess the role of this enhancer in the activation of MLC expression during development, transgenic mice were generated carrying multiple copies of a MLC1 promoter-chloramphenicol acetyltransferase (CAT) transcription unit linked to a genomic fragment including the enhancer. CAT expression was detected in four mouse lines, up to 1000-fold higher in skeletal muscles than in other tissues. Activation of endogenous MLC1 transcription in these animals 4 days before birth was reflected in the onset of CAT transgene expression. This study identifies the transcriptional control elements necessary to activate the 21-kilobase MLC1/3 locus at the appropriate fetal stage and indicates that the MLC enhancer is sufficient to induce developmentally regulated expression from the MLC1 promoter exclusively in skeletal muscle cells.
MeSH Terms
Aging
Animals
Blotting, Northern
Blotting, Southern
Cells, Cultured
Chloramphenicol O-Acetyltransferase/genetics,metabolism
Enhancer Elements, Genetic
Female
Fibroblasts/metabolism
Gene Expression Regulation
Genes
Genetic Vectors
Kinetics
Mice
Mice, Transgenic
Muscle Development
Muscles/embryology,metabolism
Myosin Subfragments/genetics
Plasmids
Rats
Transfection
Chemicals
Myosin Subfragments
Chloramphenicol O-Acetyltransferase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Rosenthal N
Department of Biochemistry, Boston University School of Medicine, MA 02118.
Kornhauser J M
Donoghue M
Rosen K M
Merlie J P
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