Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
|
pubmed:dateCreated |
1998-6-2
|
pubmed:databankReference | |
pubmed:abstractText |
We have characterized a group of cis-regulatory elements that control muscle-specific expression of the rat skeletal muscle type 1 sodium channel (SkM1) gene. These elements are located within a 3. 1-kilobase fragment that encompasses the 5'-flanking region, first exon, and part of the first intron of SkM1. We sequenced the region between -1062 and +311 and determined the start sites of transcription; multiple sites were identified between +1 and +30. The basal promoter (-65/+11) lacks cell-type specificity, while an upstream repressor (-174/-65) confers muscle-specific expression. A positive element (+49/+254) increases muscle-specific expression. Within these broad elements, two E boxes play a pivotal role. One E box at -31/-26 within the promoter, acting in part through its ability to bind the myogenic basic helix-loop-helix proteins, recruits additional factor(s) that bind elsewhere within the SkM1 sequence to control positive expression of the gene. A second E box at -90/-85 within the repressor controls negative regulation of the gene and acts through a different complex of proteins. Several of these cis-regulatory elements share both sequence and functional similarities with cis-regulatory elements of the acetylcholine receptor delta-subunit; the different arrangement of these elements may contribute to unique expression patterns for the two genes.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0021-9258
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
273
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
11327-34
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:9556626-Animals,
pubmed-meshheading:9556626-Base Sequence,
pubmed-meshheading:9556626-Cloning, Molecular,
pubmed-meshheading:9556626-DNA Footprinting,
pubmed-meshheading:9556626-Molecular Sequence Data,
pubmed-meshheading:9556626-Muscle, Skeletal,
pubmed-meshheading:9556626-MyoD Protein,
pubmed-meshheading:9556626-Myogenin,
pubmed-meshheading:9556626-Promoter Regions, Genetic,
pubmed-meshheading:9556626-Protein Binding,
pubmed-meshheading:9556626-Rats,
pubmed-meshheading:9556626-Regulatory Sequences, Nucleic Acid,
pubmed-meshheading:9556626-Sequence Deletion,
pubmed-meshheading:9556626-Sodium Channels,
pubmed-meshheading:9556626-Transcription, Genetic
|
pubmed:year |
1998
|
pubmed:articleTitle |
Two E-boxes are the focal point of muscle-specific skeletal muscle type 1 Na+ channel gene expression.
|
pubmed:affiliation |
Department of Neuroscience, University of Pennsylvania Medical School, Philadelphia, Pennsylvania 19104, USA. kraner@mail.med.upenn.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|