Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1996-10-11
pubmed:abstractText
We here report isolation of exon 1 and analysis of the human B-50 promoter. A human genomic lambda EMBL3 library was screened with a homologous PCR probe. Two independent clones were analyzed and partially sequenced: They contained up to 5 kb sequence upstream of the translation start site and approx 13 kb of intron 1 sequence. There was a high degree of homology between the rat and the human gene with 100% homology from -504 to -427, with respect to the translation start codon. However, relatively long GT and GA repeats as seen in the rat gene were absent. Various promoter-reporter constructs, containing 5.0 to 0.12 kb of the upstream region, were transfected into undifferentiated and neuroectodermally differentiated P19-EC. Two promoter activities were found. The minimal fragment with promoter activity still responsive to differentiation was the 0.22 kb construct, similar to rat promoter P2. We conclude that the human B-50 gene is expressed in a similar way to the rat B-50 gene, based on the presence of two transcripts, the high degree of homology between the rat and the human sequence, and the two promoter activities found in P19-EC cells.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0895-8696
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
109-19
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:8746449-Animals, pubmed-meshheading:8746449-Bacteriophage lambda, pubmed-meshheading:8746449-Base Sequence, pubmed-meshheading:8746449-Cell Differentiation, pubmed-meshheading:8746449-Cell Line, pubmed-meshheading:8746449-Cloning, Molecular, pubmed-meshheading:8746449-DNA Primers, pubmed-meshheading:8746449-Exons, pubmed-meshheading:8746449-GAP-43 Protein, pubmed-meshheading:8746449-Humans, pubmed-meshheading:8746449-Introns, pubmed-meshheading:8746449-Luciferases, pubmed-meshheading:8746449-Membrane Glycoproteins, pubmed-meshheading:8746449-Mice, pubmed-meshheading:8746449-Molecular Sequence Data, pubmed-meshheading:8746449-Nerve Tissue Proteins, pubmed-meshheading:8746449-Neurons, pubmed-meshheading:8746449-Oligodeoxyribonucleotides, pubmed-meshheading:8746449-Polymerase Chain Reaction, pubmed-meshheading:8746449-Promoter Regions, Genetic, pubmed-meshheading:8746449-Protein Biosynthesis, pubmed-meshheading:8746449-Rats, pubmed-meshheading:8746449-Recombinant Proteins, pubmed-meshheading:8746449-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:8746449-Restriction Mapping, pubmed-meshheading:8746449-Sequence Homology, Nucleic Acid, pubmed-meshheading:8746449-TATA Box, pubmed-meshheading:8746449-Transfection
pubmed:year
1995
pubmed:articleTitle
Cloning and promoter analysis of the human B-50/GAP-43 gene.
pubmed:affiliation
Division of Gastroenterology, Mayo Clinic and Foundation, Rochester, MN, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't