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10.1038/ki.1997.76 http://scihub22266oqcxt.onion/10.1038/ki.1997.76 9027736!ä!9027736 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=9027736&cmd=llinks): Failed to open stream: HTTP request failed! 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Erythropoietin gene regulation depends on heme-dependent oxygen sensing and assembly of interacting transcription factors |pdf=|usr=}}{{9027736}} gab.com Text Erythropoietin gene regulation depends on heme-dependent oxygen sensing and assembly of interacting transcription factors JO: Kidney Int http://www.kidney.de/pget.php?&tw=1&pmid=9027736 #FOAvip Studies on erythropoietin (Epo) gene expression have been useful in investigating the mechanism by which cells and tissues sense hypoxia. Both in vivo and in Hep3B cells. Epo production is induced not only by hypoxia but also by certain transition metal (cobalt and nickel) and by iron chelation. When Hep3B cells were incubated in an iron deficient medium, Epo mRNA expression was enhanced fourfold compared to Hep3B cells in iron enriched medium. Epo induction by cobalt was inversely related to iron concentration in the medium, indicating competition between the two metals. Under hyperbaric oxygen, cobalt induction of erythropoietin mRNA was modestly suppressed while nickel induction was markedly enhanced. These recent observations support the proposal that the oxygen sensor is a heme protein in which cobalt and nickel can substitute for iron in the porphyrin ring. The up-regulation of Epo gene transcription by hypoxia depends on at least two known DNA binding transcription factors, HIF-1 and HNF-4, which bind to cognate response elements in a critical approximately 50 bp 3' enhancer. Hypoxia induces HIF-1 binding. HNF-4, an orphan nuclear receptor constitutively expressed in kidney and liver, binds downstream of HIF-1 and cooperates with HIF-1, contributing importantly to high level and perhaps tissue specific expression. The C-terminal activation domain of HNF-4 binds to the beta subunit of HIF-1. The C-terminal portion of the alpha subunit of HIF-1 binds specifically to p300, a general transcriptional activator. Hypoxic induction of the endogenous Epo gene in Hep3B cells as well as an Epo-reporter gene was fully inhibited by E1A, an adenovirus protein that binds to and inactivates p300, but only slightly by a mutant E1A that fails to bind to p300. Moreover, overexpression of p300 enhanced hypoxic induction. Thus, it is likely that in hypoxic cells, p300 or a related family member plays a critical role in forming a macromolecular assembly with HIF-1 and HNF-4, enabling transduction from the Epo 3' enhancer to the apparatus on the promoter responsible for the initiation of transcription. Twit Text FOAVip Erythropoietin gene regulation depends on heme-dependent oxygen sensing and assembly of interacting transcription factors ????Kidney Int http://www.kidney.de/pget.php?&tw=1&pmid=9027736 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=9027736 #FOAvip English Wikipedia <ref>{{Cite pmid|9027736}}</ref> Erythropoietin gene regulation depends on heme-dependent oxygen sensing and assembly of interacting transcription factors #MMPMID9027736 Huang LE; Ho V; Arany Z; Krainc D; Galson D; Tendler D; Livingston DM; Bunn HF Kidney Int 1997[Feb]; 51 (2): 548-52 PMID9027736show ga Studies on erythropoietin (Epo) gene expression have been useful in investigating the mechanism by which cells and tissues sense hypoxia. Both in vivo and in Hep3B cells. Epo production is induced not only by hypoxia but also by certain transition metal (cobalt and nickel) and by iron chelation. When Hep3B cells were incubated in an iron deficient medium, Epo mRNA expression was enhanced fourfold compared to Hep3B cells in iron enriched medium. Epo induction by cobalt was inversely related to iron concentration in the medium, indicating competition between the two metals. Under hyperbaric oxygen, cobalt induction of erythropoietin mRNA was modestly suppressed while nickel induction was markedly enhanced. These recent observations support the proposal that the oxygen sensor is a heme protein in which cobalt and nickel can substitute for iron in the porphyrin ring. The up-regulation of Epo gene transcription by hypoxia depends on at least two known DNA binding transcription factors, HIF-1 and HNF-4, which bind to cognate response elements in a critical approximately 50 bp 3' enhancer. Hypoxia induces HIF-1 binding. HNF-4, an orphan nuclear receptor constitutively expressed in kidney and liver, binds downstream of HIF-1 and cooperates with HIF-1, contributing importantly to high level and perhaps tissue specific expression. The C-terminal activation domain of HNF-4 binds to the beta subunit of HIF-1. The C-terminal portion of the alpha subunit of HIF-1 binds specifically to p300, a general transcriptional activator. Hypoxic induction of the endogenous Epo gene in Hep3B cells as well as an Epo-reporter gene was fully inhibited by E1A, an adenovirus protein that binds to and inactivates p300, but only slightly by a mutant E1A that fails to bind to p300. Moreover, overexpression of p300 enhanced hypoxic induction. Thus, it is likely that in hypoxic cells, p300 or a related family member plays a critical role in forming a macromolecular assembly with HIF-1 and HNF-4, enabling transduction from the Epo 3' enhancer to the apparatus on the promoter responsible for the initiation of transcription. |*Gene Expression Regulation[MESH] |Basic Helix-Loop-Helix Leucine Zipper Transcription Factors[MESH] |Cell Hypoxia/genetics/physiology[MESH] |Cell Line[MESH] |DNA-Binding Proteins/chemistry/metabolism[MESH] |Erythropoietin/*genetics[MESH] |Heme/*metabolism[MESH] |Hepatocyte Nuclear Factor 4[MESH] |Humans[MESH] |Hypoxia-Inducible Factor 1[MESH] |Hypoxia-Inducible Factor 1, alpha Subunit[MESH] |Macromolecular Substances[MESH] |Models, Biological[MESH] |Nuclear Proteins/chemistry/metabolism[MESH] |Oxygen/*metabolism[MESH] |Phosphoproteins/chemistry/metabolism[MESH] |Protein Conformation[MESH] |RNA, Messenger/genetics/metabolism[MESH] |Signal Transduction[MESH]Erythropoietin gene regulation depends on heme-dependent oxygen sensin(epmc).pdf DeepDyve Pubget Overpricing