Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-4-5
pubmed:abstractText
Bach1 functions as a transcriptional repressor of heme oxygenase-1 (HO-1) and the beta-globin genes. The enhancer regions of these genes contain multiple Maf recognition elements (MAREs) to which Bach1 can bind. Previous studies have shown that increased levels of heme and cadmium induce the nuclear export of Bach1, resulting in cytoplasmic accumulation. By means of a yeast two hybrid screening using Bach1 as bait, we identified the intracellular hyaluronic acid binding protein (IHABP) as a potential regulator of Bach1. IHABP is a microtubule-associated protein that may regulate the organization of the cytoskeletal network. A series of domain analyses revealed that a region of Bach1 previously implicated in cytoplasmic accumulation was necessary for IHABP-binding. A C-terminal region of IHABP was necessary for Bach1-binding. Overexpressed Bach1 colocalized with IHABP in the cytoplasm, forming fiber-like structures on microtubules. Fluorescence recovery after photobleaching (FRAP) analysis revealed a dynamic nature of the Bach1-IHABP interaction in living cells. The repression of HO-1 reporter activity by Bach1 was attenuated by co-transfecting IHABP in a dose-dependent manner. Moreover, the overexpression of IHABP induced the endogenous HO-1 gene in NIH3T3 cells. The overall results suggest that IHABP regulates the subcelluar localization of Bach1 in order to fine-tune transactivation of Bach1 target genes such as HO-1.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD44, http://linkedlifedata.com/resource/pubmed/chemical/BACH1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Basic-Leucine Zipper Transcription..., http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Matrix Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Fanconi Anemia Complementation..., http://linkedlifedata.com/resource/pubmed/chemical/HMOX1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase (Decyclizing), http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase-1, http://linkedlifedata.com/resource/pubmed/chemical/Hmox1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/hyaluronan-mediated motility...
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0021-924X
pubmed:author
pubmed:issnType
Print
pubmed:volume
137
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
287-96
pubmed:dateRevised
2007-12-19
pubmed:meshHeading
pubmed-meshheading:15809329-Animals, pubmed-meshheading:15809329-Antigens, CD44, pubmed-meshheading:15809329-Basic-Leucine Zipper Transcription Factors, pubmed-meshheading:15809329-Binding Sites, pubmed-meshheading:15809329-Cell Line, pubmed-meshheading:15809329-Cytoplasm, pubmed-meshheading:15809329-Enzyme Repression, pubmed-meshheading:15809329-Extracellular Matrix Proteins, pubmed-meshheading:15809329-Fanconi Anemia Complementation Group Proteins, pubmed-meshheading:15809329-Fluorescence Recovery After Photobleaching, pubmed-meshheading:15809329-Heme Oxygenase (Decyclizing), pubmed-meshheading:15809329-Heme Oxygenase-1, pubmed-meshheading:15809329-Humans, pubmed-meshheading:15809329-Kidney, pubmed-meshheading:15809329-Membrane Proteins, pubmed-meshheading:15809329-Mice, pubmed-meshheading:15809329-NIH 3T3 Cells, pubmed-meshheading:15809329-Transcription Factors, pubmed-meshheading:15809329-Two-Hybrid System Techniques
pubmed:year
2005
pubmed:articleTitle
Dynamic cytoplasmic anchoring of the transcription factor Bach1 by intracellular hyaluronic acid binding protein IHABP.
pubmed:affiliation
Department of Biomedical Chemistry, Hiroshima University Graduate School of Biomedical Sciences, Kasumi 1-2-3, Hiroshima 734-8551.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't