Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
14
pubmed:dateCreated
2000-5-8
pubmed:databankReference
pubmed:abstractText
The erythroid-enriched transcription factor NF-E2 is composed of two subunits, p45 and p18, the former of which is mainly expressed in the hematopoietic system. We have isolated and characterized the mouse p45 NF-E2 gene; we show here that, similar to the human gene, the mouse gene has two alternative promoters, which are differentially active during development and in different hematopoietic cells. Transcripts from the distal promoter are present in both erythroid and myeloid cells; however, transcripts from an alternative proximal 1b promoter, lying in the first intron, are abundant in erythroid cells, but barely detectable in myeloid cells. During development, both transcripts are detectable in yolk sac, fetal liver, and bone marrow. Transfection experiments show that proximal promoter 1b has a strong activity in erythroid cells, which is completely dependent on the integrity of a palindromic GATA-1 binding site. In contrast, the distal promoter 1a is not active in this assay. When the promoter 1b is placed 3' to the promoter 1a and reporter gene, in an arrangement that resembles the natural one, it acts as an enhancer to stimulate the activity of the upstream promoter la.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Erythroid-Specific DNA-Binding..., http://linkedlifedata.com/resource/pubmed/chemical/GATA1 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/GATA1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Gata1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances, http://linkedlifedata.com/resource/pubmed/chemical/MafK Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/Mafk protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/NF-E2 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/NF-E2 Transcription Factor, p45..., http://linkedlifedata.com/resource/pubmed/chemical/NFE2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Nfe2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
7
pubmed:volume
275
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
10567-76
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10744751-Alternative Splicing, pubmed-meshheading:10744751-Animals, pubmed-meshheading:10744751-Base Sequence, pubmed-meshheading:10744751-Binding Sites, pubmed-meshheading:10744751-DNA-Binding Proteins, pubmed-meshheading:10744751-Erythroid-Specific DNA-Binding Factors, pubmed-meshheading:10744751-Exons, pubmed-meshheading:10744751-Fetus, pubmed-meshheading:10744751-GATA1 Transcription Factor, pubmed-meshheading:10744751-Gene Expression Regulation, pubmed-meshheading:10744751-Humans, pubmed-meshheading:10744751-Introns, pubmed-meshheading:10744751-Macromolecular Substances, pubmed-meshheading:10744751-MafK Transcription Factor, pubmed-meshheading:10744751-Mice, pubmed-meshheading:10744751-Molecular Sequence Data, pubmed-meshheading:10744751-NF-E2 Transcription Factor, pubmed-meshheading:10744751-NF-E2 Transcription Factor, p45 Subunit, pubmed-meshheading:10744751-Nuclear Proteins, pubmed-meshheading:10744751-Promoter Regions, Genetic, pubmed-meshheading:10744751-Sequence Alignment, pubmed-meshheading:10744751-Sequence Homology, Nucleic Acid, pubmed-meshheading:10744751-Transcription, Genetic, pubmed-meshheading:10744751-Transcription Factors
pubmed:year
2000
pubmed:articleTitle
Regulation of mouse p45 NF-E2 transcription by an erythroid-specific GATA-dependent intronic alternative promoter.
pubmed:affiliation
Centro di Studio sulla Patologia Cellulare, Consiglio Nazionale delle Ricerche, Istituto di Patologia Generale, Università di Milano, Via Mangiagalli, 31, 20133 Milano, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't