Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1996-4-26
pubmed:abstractText
AP-1/NF-E2 motifs found in erythroid transcription control elements are associated with powerful transcription activation and thought to be regulated by the erythroid transcription factor NF-E2. We have studied AP-1/NF-E2 motifs from three different erythroid control elements (5'HS2 of the human beta-globin locus control region [LCR], the porphobilinogen deaminase [PBGD] promoter, and the mouse Band 3 promoter). We find that these AP-1/NF-E2 elements differ both in their ability to bind NF-E2 and their activity in transient assays. Each of the elements is bound by AP-1, but only the 5'HS2 and PBGD sites are bound by NF-E2. We examined the activity of these sites in minimal promoter constructs in transient assays. In erythroid cells, activity of duplicated NF-E2 motifs is positively correlated with binding by NF-E2; however, the Band 3 element not bound by NF-E2 is also active in some contexts. In HeLa cells, all sites were active and duplicated sites were most active. In F9 mouse teratocarcinoma cells, which express neither NF-E2 nor AP-1, the elements' activity parallels that in erythroid cells. While these finding are consistent with other evidence that NF-E2 is an important regulator of erythroid transcription, they suggest that some sites that resemble NF-E2 elements are actually regulated by other factors; we speculate that other tissue-specific and/or generally expressed factors may act on these sites.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0301-472X
pubmed:author
pubmed:issnType
Print
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
445-52
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:8599974-Animals, pubmed-meshheading:8599974-Base Sequence, pubmed-meshheading:8599974-Binding, Competitive, pubmed-meshheading:8599974-Binding Sites, pubmed-meshheading:8599974-DNA, pubmed-meshheading:8599974-DNA-Binding Proteins, pubmed-meshheading:8599974-Erythroid-Specific DNA-Binding Factors, pubmed-meshheading:8599974-Globins, pubmed-meshheading:8599974-HeLa Cells, pubmed-meshheading:8599974-Humans, pubmed-meshheading:8599974-Leukemia, Erythroblastic, Acute, pubmed-meshheading:8599974-Mice, pubmed-meshheading:8599974-Molecular Sequence Data, pubmed-meshheading:8599974-NF-E2 Transcription Factor, pubmed-meshheading:8599974-NF-E2 Transcription Factor, p45 Subunit, pubmed-meshheading:8599974-Promoter Regions, Genetic, pubmed-meshheading:8599974-Rabbits, pubmed-meshheading:8599974-Regulatory Sequences, Nucleic Acid, pubmed-meshheading:8599974-Transcription Factor AP-1, pubmed-meshheading:8599974-Transcription Factors, pubmed-meshheading:8599974-Tumor Cells, Cultured
pubmed:year
1996
pubmed:articleTitle
Erythroid AP-1/NF-E2 elements vary in their response to NF-E2.
pubmed:affiliation
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't