Source:http://linkedlifedata.com/resource/pubmed/id/18308612
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0005221,
umls-concept:C0007600,
umls-concept:C0017255,
umls-concept:C0017337,
umls-concept:C0042679,
umls-concept:C0086597,
umls-concept:C0205177,
umls-concept:C0218530,
umls-concept:C1416968,
umls-concept:C1417108,
umls-concept:C1417699,
umls-concept:C1514583,
umls-concept:C1514873,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C1706553
|
pubmed:issue |
8
|
pubmed:dateCreated |
2008-5-5
|
pubmed:abstractText |
Evidences indicate that locus control region (LCR) of beta-globin spatially closes to the downstream active gene promoter to mediate the transcriptional activation by looping. DNA binding proteins may play an important role in the looping formation. NF-E2 is one of the key transcription factors in beta-globin gene transcriptional activation. To shed light on whether NF-E2 is involved in this process, DS19MafKsiRNA cell pools were established by specifically knocked down the expression of MafK/NF-E2 p18, one subunit of NF-E2 heterodimer. In the above cell pools, it was observed that the occupancy efficiency of NF-E2 on beta-globin gene locus and the expression level of beta-globin genes were decreased. H3 acetylation, H3-K4 methylation and the deposition of RNA polymerase II, but not the recruitment of GATA-1, were also found reduced at the beta-globin gene cluster. Chromosome Conformation Capture (3C) assay showed that the cross-linking frequency between the main NF-E2 binding site HS2 and downstream structural genes was reduced compared to the normal cell. This result demonstrated that MafK/NF-E2 p18 recruitment was involved in the physical proximity of LCR and active beta-globin genes upon beta-globin gene transcriptional activation.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA Polymerase II,
http://linkedlifedata.com/resource/pubmed/chemical/GATA1 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Gata1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Globins,
http://linkedlifedata.com/resource/pubmed/chemical/Histones,
http://linkedlifedata.com/resource/pubmed/chemical/MafK Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Mafk protein, mouse
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1357-2725
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
40
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1481-93
|
pubmed:meshHeading |
pubmed-meshheading:18308612-Animals,
pubmed-meshheading:18308612-Cell Line, Tumor,
pubmed-meshheading:18308612-Chromatin Immunoprecipitation,
pubmed-meshheading:18308612-DNA Polymerase II,
pubmed-meshheading:18308612-GATA1 Transcription Factor,
pubmed-meshheading:18308612-Gene Expression Regulation,
pubmed-meshheading:18308612-Gene Silencing,
pubmed-meshheading:18308612-Globins,
pubmed-meshheading:18308612-Histones,
pubmed-meshheading:18308612-Locus Control Region,
pubmed-meshheading:18308612-MafK Transcription Factor,
pubmed-meshheading:18308612-Mice,
pubmed-meshheading:18308612-RNA Interference
|
pubmed:year |
2008
|
pubmed:articleTitle |
MafK/NF-E2 p18 is required for beta-globin genes activation by mediating the proximity of LCR and active beta-globin genes in MEL cell line.
|
pubmed:affiliation |
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, PR China.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|