Loading…

Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity

The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in cell and developmental biology 2016-02, Vol.4, p.11-11
Main Authors: Kietzmann, Thomas, Mennerich, Daniela, Dimova, Elitsa Y
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863
cites cdi_FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863
container_end_page 11
container_issue
container_start_page 11
container_title Frontiers in cell and developmental biology
container_volume 4
creator Kietzmann, Thomas
Mennerich, Daniela
Dimova, Elitsa Y
description The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation.
doi_str_mv 10.3389/fcell.2016.00011
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3aa4defc4e4b42c8a856c91ab3012648</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_3aa4defc4e4b42c8a856c91ab3012648</doaj_id><sourcerecordid>1770877359</sourcerecordid><originalsourceid>FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863</originalsourceid><addsrcrecordid>eNpVkc9rFDEYhoMottTePckcK3TW_JjJJB4EKa47sKBgBW_hSybpZpmdjMlscf3rzc7W0p4Skud98pEXobcELxgT8oMztu8XFBO-wBgT8gKdUyp5yVn16-WT_Rm6TGl7RGjd1IK9RmeUy4qSRp6j7eowhj8eynbo9sbr3hZLMFOIqbhatcv0voChK75vQho3IR56mHwYPhbtbsxUEYbixwTa9346XBfrYKD3f2fkes7dRhhSBv19Bt6gVw76ZC8f1gv0c_nl9mZVrr99bW8-r0tTUzGVUrquAyowNdoSrB2rGl4LUnNHgXMumeBau6qz1BgtBWHUOUM7pl1Xa8HZBWpP3i7AVo3R7yAeVACv5oMQ7xTEyZveKgaQPc5UttIVNQJEzY0koFn-LF6J7Pp0co17vbOdscMUoX8mfX4z-I26C_cqz8ywaLLg6kEQw--9TZPa-XQsDgYb9kmRpslYw2qZUXxCTQwpResenyFYHRtXc-Pq2LiaG8-Rd0_Hewz875f9Ayxrqg0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1770877359</pqid></control><display><type>article</type><title>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</title><source>PubMed Central</source><creator>Kietzmann, Thomas ; Mennerich, Daniela ; Dimova, Elitsa Y</creator><creatorcontrib>Kietzmann, Thomas ; Mennerich, Daniela ; Dimova, Elitsa Y</creatorcontrib><description>The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation.</description><identifier>ISSN: 2296-634X</identifier><identifier>EISSN: 2296-634X</identifier><identifier>DOI: 10.3389/fcell.2016.00011</identifier><identifier>PMID: 26942179</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>HIF-1α ; hypoxia ; kinase ; MAPK pathway ; Oncology ; Phosphorylation ; PI3K/PKB pathway</subject><ispartof>Frontiers in cell and developmental biology, 2016-02, Vol.4, p.11-11</ispartof><rights>Copyright © 2016 Kietzmann, Mennerich and Dimova. 2016 Kietzmann, Mennerich and Dimova</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863</citedby><cites>FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763087/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763087/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26942179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kietzmann, Thomas</creatorcontrib><creatorcontrib>Mennerich, Daniela</creatorcontrib><creatorcontrib>Dimova, Elitsa Y</creatorcontrib><title>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</title><title>Frontiers in cell and developmental biology</title><addtitle>Front Cell Dev Biol</addtitle><description>The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation.</description><subject>HIF-1α</subject><subject>hypoxia</subject><subject>kinase</subject><subject>MAPK pathway</subject><subject>Oncology</subject><subject>Phosphorylation</subject><subject>PI3K/PKB pathway</subject><issn>2296-634X</issn><issn>2296-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc9rFDEYhoMottTePckcK3TW_JjJJB4EKa47sKBgBW_hSybpZpmdjMlscf3rzc7W0p4Skud98pEXobcELxgT8oMztu8XFBO-wBgT8gKdUyp5yVn16-WT_Rm6TGl7RGjd1IK9RmeUy4qSRp6j7eowhj8eynbo9sbr3hZLMFOIqbhatcv0voChK75vQho3IR56mHwYPhbtbsxUEYbixwTa9346XBfrYKD3f2fkes7dRhhSBv19Bt6gVw76ZC8f1gv0c_nl9mZVrr99bW8-r0tTUzGVUrquAyowNdoSrB2rGl4LUnNHgXMumeBau6qz1BgtBWHUOUM7pl1Xa8HZBWpP3i7AVo3R7yAeVACv5oMQ7xTEyZveKgaQPc5UttIVNQJEzY0koFn-LF6J7Pp0co17vbOdscMUoX8mfX4z-I26C_cqz8ywaLLg6kEQw--9TZPa-XQsDgYb9kmRpslYw2qZUXxCTQwpResenyFYHRtXc-Pq2LiaG8-Rd0_Hewz875f9Ayxrqg0</recordid><startdate>20160223</startdate><enddate>20160223</enddate><creator>Kietzmann, Thomas</creator><creator>Mennerich, Daniela</creator><creator>Dimova, Elitsa Y</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160223</creationdate><title>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</title><author>Kietzmann, Thomas ; Mennerich, Daniela ; Dimova, Elitsa Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>HIF-1α</topic><topic>hypoxia</topic><topic>kinase</topic><topic>MAPK pathway</topic><topic>Oncology</topic><topic>Phosphorylation</topic><topic>PI3K/PKB pathway</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kietzmann, Thomas</creatorcontrib><creatorcontrib>Mennerich, Daniela</creatorcontrib><creatorcontrib>Dimova, Elitsa Y</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in cell and developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kietzmann, Thomas</au><au>Mennerich, Daniela</au><au>Dimova, Elitsa Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity</atitle><jtitle>Frontiers in cell and developmental biology</jtitle><addtitle>Front Cell Dev Biol</addtitle><date>2016-02-23</date><risdate>2016</risdate><volume>4</volume><spage>11</spage><epage>11</epage><pages>11-11</pages><issn>2296-634X</issn><eissn>2296-634X</eissn><abstract>The hypoxia-inducible factor α-subunits (HIFα) are key transcription factors in the mammalian response to oxygen deficiency. The HIFα regulation in response to hypoxia occurs primarily on the level of protein stability due to posttranslational hydroxylation and proteasomal degradation. However, HIF α-subunits also respond to various growth factors, hormones, or cytokines under normoxia indicating involvement of different kinase pathways in their regulation. Because these proteins participate in angiogenesis, glycolysis, programmed cell death, cancer, and ischemia, HIFα regulating kinases are attractive therapeutic targets. Although numerous kinases were reported to regulate HIFα indirectly, direct phosphorylation of HIFα affects HIFα stability, nuclear localization, and transactivity. Herein, we review the role of phosphorylation-dependent HIFα regulation with emphasis on protein stability, subcellular localization, and transactivation.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>26942179</pmid><doi>10.3389/fcell.2016.00011</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2296-634X
ispartof Frontiers in cell and developmental biology, 2016-02, Vol.4, p.11-11
issn 2296-634X
2296-634X
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_3aa4defc4e4b42c8a856c91ab3012648
source PubMed Central
subjects HIF-1α
hypoxia
kinase
MAPK pathway
Oncology
Phosphorylation
PI3K/PKB pathway
title Hypoxia-Inducible Factors (HIFs) and Phosphorylation: Impact on Stability, Localization, and Transactivity
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T18%3A38%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hypoxia-Inducible%20Factors%20(HIFs)%20and%20Phosphorylation:%20Impact%20on%20Stability,%20Localization,%20and%20Transactivity&rft.jtitle=Frontiers%20in%20cell%20and%20developmental%20biology&rft.au=Kietzmann,%20Thomas&rft.date=2016-02-23&rft.volume=4&rft.spage=11&rft.epage=11&rft.pages=11-11&rft.issn=2296-634X&rft.eissn=2296-634X&rft_id=info:doi/10.3389/fcell.2016.00011&rft_dat=%3Cproquest_doaj_%3E1770877359%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c528t-99fdda2802cbe10bf347658156f2a6669386bbf4de2ccb98132ffc2d3bfd5b863%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1770877359&rft_id=info:pmid/26942179&rfr_iscdi=true