Corticosterone Actions on the Hippocampal Brain-Derived Neurotrophic Factor Expression are Mediated by Exon IV Promoter
Brain‐derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco‐ and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid‐mediated gene reg...
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description | Brain‐derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco‐ and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid‐mediated gene regulation. In adrenalectomised rats, corticosterone (10 mg/kg s.c.) induces a robust down‐regulation of both BDNF mRNA and protein levels in the hippocampus peaking at 2–8 h. To study the role of the individual promoters in the corticosterone response, we employed exon‐specific riboprobe in situ hybridisation as well as real‐time polymerase chain reaction (PCR) in the dentate gyrus. We found a down‐regulation, mainly of exon IV and the protein‐coding exon V, in nearby all hippocampal subregions, but exon II was only down‐regulated in the dentate gyrus. Exon I and exon III transcripts were not affected by corticosterone treatment. The results could be confirmed with real‐time PCR in the dentate gyrus. It appears as if the exon IV promoter is the major target for corticosterone‐mediated transcriptional regulation of BDNF in the hippocampus. |
doi_str_mv | 10.1111/j.1365-2826.2005.01390.x |
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C. ; Sommer, W. H. ; Metsis, M. ; Strömberg, I. ; Agnati, L. F. ; Fuxe, K.</creator><creatorcontrib>Hansson, A. C. ; Sommer, W. H. ; Metsis, M. ; Strömberg, I. ; Agnati, L. F. ; Fuxe, K.</creatorcontrib><description>Brain‐derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco‐ and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid‐mediated gene regulation. In adrenalectomised rats, corticosterone (10 mg/kg s.c.) induces a robust down‐regulation of both BDNF mRNA and protein levels in the hippocampus peaking at 2–8 h. To study the role of the individual promoters in the corticosterone response, we employed exon‐specific riboprobe in situ hybridisation as well as real‐time polymerase chain reaction (PCR) in the dentate gyrus. We found a down‐regulation, mainly of exon IV and the protein‐coding exon V, in nearby all hippocampal subregions, but exon II was only down‐regulated in the dentate gyrus. Exon I and exon III transcripts were not affected by corticosterone treatment. The results could be confirmed with real‐time PCR in the dentate gyrus. It appears as if the exon IV promoter is the major target for corticosterone‐mediated transcriptional regulation of BDNF in the hippocampus.</description><identifier>ISSN: 0953-8194</identifier><identifier>ISSN: 1365-2826</identifier><identifier>EISSN: 1365-2826</identifier><identifier>DOI: 10.1111/j.1365-2826.2005.01390.x</identifier><identifier>PMID: 16420279</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adrenalectomy ; Analysis of Variance ; Animals ; Biological and medical sciences ; brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - genetics ; Brain-Derived Neurotrophic Factor - metabolism ; Brain-Derived Neurotrophic Factor/genetics/metabolism ; Corticosterone - blood ; Corticosterone - physiology ; Corticosterone/blood/physiology ; Down-Regulation ; Exons - genetics ; Exons - physiology ; Exons/genetics/physiology ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation - physiology ; glucocorticoids ; Hippocampus - metabolism ; Male ; neurotrophin ; Promoter Regions (Genetics)/physiology ; Promoter Regions, Genetic - physiology ; rat brain ; rat brain neurotrophin ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - analysis ; Time Factors ; Transcription, Genetic - physiology ; Vertebrates: endocrinology</subject><ispartof>Journal of neuroendocrinology, 2006-02, Vol.18 (2), p.104-114</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Feb 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6340-83063bdf89260b10cce01b2fe63ac62ea1d0666464b316d8a118f36d4771acd13</citedby><cites>FETCH-LOGICAL-c6340-83063bdf89260b10cce01b2fe63ac62ea1d0666464b316d8a118f36d4771acd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2826.2005.01390.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2826.2005.01390.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,777,781,882,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17577761$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16420279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-12294$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1944275$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Hansson, A. C.</creatorcontrib><creatorcontrib>Sommer, W. H.</creatorcontrib><creatorcontrib>Metsis, M.</creatorcontrib><creatorcontrib>Strömberg, I.</creatorcontrib><creatorcontrib>Agnati, L. F.</creatorcontrib><creatorcontrib>Fuxe, K.</creatorcontrib><title>Corticosterone Actions on the Hippocampal Brain-Derived Neurotrophic Factor Expression are Mediated by Exon IV Promoter</title><title>Journal of neuroendocrinology</title><addtitle>J Neuroendocrinol</addtitle><description>Brain‐derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco‐ and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid‐mediated gene regulation. In adrenalectomised rats, corticosterone (10 mg/kg s.c.) induces a robust down‐regulation of both BDNF mRNA and protein levels in the hippocampus peaking at 2–8 h. To study the role of the individual promoters in the corticosterone response, we employed exon‐specific riboprobe in situ hybridisation as well as real‐time polymerase chain reaction (PCR) in the dentate gyrus. We found a down‐regulation, mainly of exon IV and the protein‐coding exon V, in nearby all hippocampal subregions, but exon II was only down‐regulated in the dentate gyrus. Exon I and exon III transcripts were not affected by corticosterone treatment. The results could be confirmed with real‐time PCR in the dentate gyrus. It appears as if the exon IV promoter is the major target for corticosterone‐mediated transcriptional regulation of BDNF in the hippocampus.</description><subject>Adrenalectomy</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Brain-Derived Neurotrophic Factor/genetics/metabolism</subject><subject>Corticosterone - blood</subject><subject>Corticosterone - physiology</subject><subject>Corticosterone/blood/physiology</subject><subject>Down-Regulation</subject><subject>Exons - genetics</subject><subject>Exons - physiology</subject><subject>Exons/genetics/physiology</subject><subject>Fundamental and applied biological sciences. 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C.</creator><creator>Sommer, W. H.</creator><creator>Metsis, M.</creator><creator>Strömberg, I.</creator><creator>Agnati, L. F.</creator><creator>Fuxe, K.</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D93</scope></search><sort><creationdate>200602</creationdate><title>Corticosterone Actions on the Hippocampal Brain-Derived Neurotrophic Factor Expression are Mediated by Exon IV Promoter</title><author>Hansson, A. C. ; Sommer, W. H. ; Metsis, M. ; Strömberg, I. ; Agnati, L. 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C.</au><au>Sommer, W. H.</au><au>Metsis, M.</au><au>Strömberg, I.</au><au>Agnati, L. F.</au><au>Fuxe, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corticosterone Actions on the Hippocampal Brain-Derived Neurotrophic Factor Expression are Mediated by Exon IV Promoter</atitle><jtitle>Journal of neuroendocrinology</jtitle><addtitle>J Neuroendocrinol</addtitle><date>2006-02</date><risdate>2006</risdate><volume>18</volume><issue>2</issue><spage>104</spage><epage>114</epage><pages>104-114</pages><issn>0953-8194</issn><issn>1365-2826</issn><eissn>1365-2826</eissn><abstract>Brain‐derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco‐ and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid‐mediated gene regulation. In adrenalectomised rats, corticosterone (10 mg/kg s.c.) induces a robust down‐regulation of both BDNF mRNA and protein levels in the hippocampus peaking at 2–8 h. To study the role of the individual promoters in the corticosterone response, we employed exon‐specific riboprobe in situ hybridisation as well as real‐time polymerase chain reaction (PCR) in the dentate gyrus. We found a down‐regulation, mainly of exon IV and the protein‐coding exon V, in nearby all hippocampal subregions, but exon II was only down‐regulated in the dentate gyrus. Exon I and exon III transcripts were not affected by corticosterone treatment. The results could be confirmed with real‐time PCR in the dentate gyrus. It appears as if the exon IV promoter is the major target for corticosterone‐mediated transcriptional regulation of BDNF in the hippocampus.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>16420279</pmid><doi>10.1111/j.1365-2826.2005.01390.x</doi><tpages>11</tpages></addata></record> |
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subjects | Adrenalectomy Analysis of Variance Animals Biological and medical sciences brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - genetics Brain-Derived Neurotrophic Factor - metabolism Brain-Derived Neurotrophic Factor/genetics/metabolism Corticosterone - blood Corticosterone - physiology Corticosterone/blood/physiology Down-Regulation Exons - genetics Exons - physiology Exons/genetics/physiology Fundamental and applied biological sciences. Psychology Gene Expression Regulation - physiology glucocorticoids Hippocampus - metabolism Male neurotrophin Promoter Regions (Genetics)/physiology Promoter Regions, Genetic - physiology rat brain rat brain neurotrophin Rats Rats, Sprague-Dawley RNA, Messenger - analysis Time Factors Transcription, Genetic - physiology Vertebrates: endocrinology |
title | Corticosterone Actions on the Hippocampal Brain-Derived Neurotrophic Factor Expression are Mediated by Exon IV Promoter |
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