Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
16
pubmed:dateCreated
2011-8-17
pubmed:abstractText
Hypoxia stabilizes the tumour suppressor p53, allowing it to function primarily as a transrepressor; however, the function of p53 during hypoxia remains unclear. In this study, we showed that p53 suppressed BNIP3 expression by directly binding to the p53-response element motif and recruiting corepressor mSin3a to the BNIP3 promoter. The DNA-binding site of p53 must remain intact for the protein to suppress the BNIP3 promoter. In addition, taking advantage of zebrafish as an in vivo model, we confirmed that zebrafish nip3a, a homologous gene of mammalian BNIP3, was indeed induced by hypoxia and p53 mutation/knockdown enhanced nip3a expression under hypoxia resulted in cell death enhancement in p53 mutant embryos. Furthermore, p53 protected against hypoxia-induced cell death mediated by p53 suppression of BNIP3 as illustrated by p53 knockdown/loss assays in both human cell lines and zebrafish model, which is in contrast to the traditional pro-apoptotic role of p53. Our results suggest a novel function of p53 in hypoxia-induced cell death, leading to the development of new treatments for ischaemic heart disease and cerebral stroke.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1460-2075
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3397-415
pubmed:meshHeading
pubmed-meshheading:21792176-Amino Acid Sequence, pubmed-meshheading:21792176-Animals, pubmed-meshheading:21792176-Apoptosis, pubmed-meshheading:21792176-Autophagy, pubmed-meshheading:21792176-Binding Sites, pubmed-meshheading:21792176-Cell Hypoxia, pubmed-meshheading:21792176-Cell Line, pubmed-meshheading:21792176-Gene Expression Regulation, pubmed-meshheading:21792176-Gene Knockdown Techniques, pubmed-meshheading:21792176-Humans, pubmed-meshheading:21792176-Membrane Proteins, pubmed-meshheading:21792176-Molecular Sequence Data, pubmed-meshheading:21792176-Promoter Regions, Genetic, pubmed-meshheading:21792176-Proto-Oncogene Proteins, pubmed-meshheading:21792176-Recombinant Fusion Proteins, pubmed-meshheading:21792176-Response Elements, pubmed-meshheading:21792176-Sequence Alignment, pubmed-meshheading:21792176-Sequence Homology, Amino Acid, pubmed-meshheading:21792176-Tumor Suppressor Protein p53, pubmed-meshheading:21792176-Zebrafish, pubmed-meshheading:21792176-Zebrafish Proteins
pubmed:year
2011
pubmed:articleTitle
p53 directly suppresses BNIP3 expression to protect against hypoxia-induced cell death.
pubmed:affiliation
Key Laboratory of Biodiversity and Conservation of Aquatic Organisms, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, PR China.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't