Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus
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Publication Date: | 2014 |
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Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1523/JNEUROSCI.4343-13.2014 http://hdl.handle.net/11449/111239 |
Summary: | Arginine vasopressin (AVP) is a neurohypophysial hormone regulating hydromineral homeostasis. Here we show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a transcription factor of the CREB/activating transcription factor (ATF) family, increases in expression in parallel with AVP expression in supraoptic nuclei (SONs) and paraventicular nuclei (PVNs) of dehydrated (DH) and salt-loaded (SL) rats, compared with euhydrated (EH) controls. In EH animals, CREB3L1 protein is expressed in glial cells, but only at a low level in SON and PVN neurons, whereas robust upregulation in AVP neurons accompanied DH and SL rats. Concomitantly, CREB3L1 is activated by cleavage, with the N-terminal domain translocating from the Golgi, via the cytosol, to the nucleus. We also show that CREB3L1 mRNA levels correlate with AVP transcription level in SONs and PVNs following sodium depletion, and as a consequence of diurnal rhythm in the suprachiasmatic nucleus. We tested the hypothesis that CREB3L1 activates AVP gene transcription. Both full-length and constitutively active forms of CREB3L1 (CREB3L1CA) induce the expression of rat AVP promoter-luciferase reporter constructs, whereas a dominant-negative mutant reduces expression. Rat AVP promoter deletion constructs revealed that CRE-like and G-box sequences in the region between -170 and -120 bp are important for CREB3L1 actions. Direct binding of CREB3L1 to the AVP promoter was shown by chromatin immunoprecipitation both in vitro and in the SON itself. Injection of a lentiviral vector expressing CREB3L1CA into rat SONs and PVNs resulted in increased AVP biosynthesis. We thus identify CREB3L1 as a regulator of AVP transcription in the rat hypothalamus. |
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Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat HypothalamusCREB3L1hyperosmotic stresshypothalamustranscriptionvasopressinArginine vasopressin (AVP) is a neurohypophysial hormone regulating hydromineral homeostasis. Here we show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a transcription factor of the CREB/activating transcription factor (ATF) family, increases in expression in parallel with AVP expression in supraoptic nuclei (SONs) and paraventicular nuclei (PVNs) of dehydrated (DH) and salt-loaded (SL) rats, compared with euhydrated (EH) controls. In EH animals, CREB3L1 protein is expressed in glial cells, but only at a low level in SON and PVN neurons, whereas robust upregulation in AVP neurons accompanied DH and SL rats. Concomitantly, CREB3L1 is activated by cleavage, with the N-terminal domain translocating from the Golgi, via the cytosol, to the nucleus. We also show that CREB3L1 mRNA levels correlate with AVP transcription level in SONs and PVNs following sodium depletion, and as a consequence of diurnal rhythm in the suprachiasmatic nucleus. We tested the hypothesis that CREB3L1 activates AVP gene transcription. Both full-length and constitutively active forms of CREB3L1 (CREB3L1CA) induce the expression of rat AVP promoter-luciferase reporter constructs, whereas a dominant-negative mutant reduces expression. Rat AVP promoter deletion constructs revealed that CRE-like and G-box sequences in the region between -170 and -120 bp are important for CREB3L1 actions. Direct binding of CREB3L1 to the AVP promoter was shown by chromatin immunoprecipitation both in vitro and in the SON itself. Injection of a lentiviral vector expressing CREB3L1CA into rat SONs and PVNs resulted in increased AVP biosynthesis. We thus identify CREB3L1 as a regulator of AVP transcription in the rat hypothalamus.Medical Research CouncilBiotechnology and Biological Sciences Research CouncilFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)University of Malaya (HIR)Univ Bristol, Sch Clin Sci, Bristol BS1 3NY, Avon, EnglandSao Paulo State Univ, Dept Physiol & Pathol, Sch Dent, BR-14801385 Sao Paulo, BrazilUniv Bristol, Sch Physiol & Pharmacol, Bristol BS8 1TD, Avon, EnglandUniv Malaya, Dept Physiol, Kuala Lumpur 50603, MalaysiaSao Paulo State Univ, Dept Physiol & Pathol, Sch Dent, BR-14801385 Sao Paulo, BrazilMedical Research CouncilG0700954Biotechnology and Biological Sciences Research CouncilBB/G006156/1Biotechnology and Biological Sciences Research CouncilBB/J01515/1FAPESP: 11/50770-1University of Malaya (HIR)H-20001-E000086Soc NeuroscienceUniv BristolUniversidade Estadual Paulista (Unesp)Univ MalayaGreenwood, MingkwanBordieri, LoredanaGreenwood, Michael P.Melo, Mariana Rosso [UNESP]Colombari, Debora S. A. [UNESP]Colombari, Eduardo [UNESP]Paton, Julian F. R.Murphy, David2014-12-03T13:07:05Z2014-12-03T13:07:05Z2014-03-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article3810-3820application/pdfhttp://dx.doi.org/10.1523/JNEUROSCI.4343-13.2014Journal Of Neuroscience. Washington: Soc Neuroscience, v. 34, n. 11, p. 3810-3820, 2014.0270-6474http://hdl.handle.net/11449/11123910.1523/JNEUROSCI.4343-13.2014WOS:000332879500002WOS000332879500002.pdf4544450092427426Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Neuroscience5.9704,466info:eu-repo/semantics/openAccess2025-04-18T09:43:42Zoai:repositorio.unesp.br:11449/111239Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-18T09:43:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
title |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
spellingShingle |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus Greenwood, Mingkwan CREB3L1 hyperosmotic stress hypothalamus transcription vasopressin |
title_short |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
title_full |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
title_fullStr |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
title_full_unstemmed |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
title_sort |
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus |
author |
Greenwood, Mingkwan |
author_facet |
Greenwood, Mingkwan Bordieri, Loredana Greenwood, Michael P. Melo, Mariana Rosso [UNESP] Colombari, Debora S. A. [UNESP] Colombari, Eduardo [UNESP] Paton, Julian F. R. Murphy, David |
author_role |
author |
author2 |
Bordieri, Loredana Greenwood, Michael P. Melo, Mariana Rosso [UNESP] Colombari, Debora S. A. [UNESP] Colombari, Eduardo [UNESP] Paton, Julian F. R. Murphy, David |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Bristol Universidade Estadual Paulista (Unesp) Univ Malaya |
dc.contributor.author.fl_str_mv |
Greenwood, Mingkwan Bordieri, Loredana Greenwood, Michael P. Melo, Mariana Rosso [UNESP] Colombari, Debora S. A. [UNESP] Colombari, Eduardo [UNESP] Paton, Julian F. R. Murphy, David |
dc.subject.por.fl_str_mv |
CREB3L1 hyperosmotic stress hypothalamus transcription vasopressin |
topic |
CREB3L1 hyperosmotic stress hypothalamus transcription vasopressin |
description |
Arginine vasopressin (AVP) is a neurohypophysial hormone regulating hydromineral homeostasis. Here we show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a transcription factor of the CREB/activating transcription factor (ATF) family, increases in expression in parallel with AVP expression in supraoptic nuclei (SONs) and paraventicular nuclei (PVNs) of dehydrated (DH) and salt-loaded (SL) rats, compared with euhydrated (EH) controls. In EH animals, CREB3L1 protein is expressed in glial cells, but only at a low level in SON and PVN neurons, whereas robust upregulation in AVP neurons accompanied DH and SL rats. Concomitantly, CREB3L1 is activated by cleavage, with the N-terminal domain translocating from the Golgi, via the cytosol, to the nucleus. We also show that CREB3L1 mRNA levels correlate with AVP transcription level in SONs and PVNs following sodium depletion, and as a consequence of diurnal rhythm in the suprachiasmatic nucleus. We tested the hypothesis that CREB3L1 activates AVP gene transcription. Both full-length and constitutively active forms of CREB3L1 (CREB3L1CA) induce the expression of rat AVP promoter-luciferase reporter constructs, whereas a dominant-negative mutant reduces expression. Rat AVP promoter deletion constructs revealed that CRE-like and G-box sequences in the region between -170 and -120 bp are important for CREB3L1 actions. Direct binding of CREB3L1 to the AVP promoter was shown by chromatin immunoprecipitation both in vitro and in the SON itself. Injection of a lentiviral vector expressing CREB3L1CA into rat SONs and PVNs resulted in increased AVP biosynthesis. We thus identify CREB3L1 as a regulator of AVP transcription in the rat hypothalamus. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-12-03T13:07:05Z 2014-12-03T13:07:05Z 2014-03-12 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1523/JNEUROSCI.4343-13.2014 Journal Of Neuroscience. Washington: Soc Neuroscience, v. 34, n. 11, p. 3810-3820, 2014. 0270-6474 http://hdl.handle.net/11449/111239 10.1523/JNEUROSCI.4343-13.2014 WOS:000332879500002 WOS000332879500002.pdf 4544450092427426 |
url |
http://dx.doi.org/10.1523/JNEUROSCI.4343-13.2014 http://hdl.handle.net/11449/111239 |
identifier_str_mv |
Journal Of Neuroscience. Washington: Soc Neuroscience, v. 34, n. 11, p. 3810-3820, 2014. 0270-6474 10.1523/JNEUROSCI.4343-13.2014 WOS:000332879500002 WOS000332879500002.pdf 4544450092427426 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Neuroscience 5.970 4,466 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
3810-3820 application/pdf |
dc.publisher.none.fl_str_mv |
Soc Neuroscience |
publisher.none.fl_str_mv |
Soc Neuroscience |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1834482910960287744 |