Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/50821
Campo DC Valoridioma
dc.contributor.authorMorales, V.en_US
dc.contributor.authorGonzalez Robayna, I.en_US
dc.contributor.authorHernandez, Ien_US
dc.contributor.authorQuintana, Jen_US
dc.contributor.authorSantana, P.en_US
dc.contributor.authorRuiz De Galarreta Hernandez,C. Manuelen_US
dc.contributor.authorFanjul Rodríguez, Luisa Fernandaen_US
dc.contributor.otherHernandez Gonzalez, Inmaculada-
dc.contributor.otherQuintana, Jose-
dc.contributor.otherGonzalez Robayna, Ignacio-
dc.date.accessioned2018-11-24T19:07:57Z-
dc.date.available2018-11-24T19:07:57Z-
dc.date.issued2003en_US
dc.identifier.issn0022-0795en_US
dc.identifier.urihttp://hdl.handle.net/10553/50821-
dc.description.abstractThe synthesis of estradiol by the granulosa cells is a prominent event in ovarian physiology and depends on the expression of P450(AROM). FSH induces the expression of P450(AROM) in granulosa cells as a result of the presence in the ovarian promoter of a CRE (cAMP response element)like sequence (CLS). In rodents, LH downregulates aromatase expression during luteinization by an as yet undescribed mechanism. In granulosa cells, LH increases the expression of the inducible cAMP early repressor (ICER), an isoform of CREM (cAMP-responsive element modulator) that represses cAMP-induced transcription. The possibility that ICER represses the activity of the aromatase ovarian promoter, thus being part of the mechanism underlying the effects of LH was investigated. We have found that: (1) nuclear proteins from forskolin-stimulated granulosa cells were specifically bound to an oligonucleotide containing the CLS sequence of the CYP19 ovarian promoter and one out of the two protein-DNA complexes formed was supershifted by an anti-REM antibody; (2) in granulosa cells, forskolin-induced increases in P450(AROM) promoter luciferase reporter gene activity were prevented by the transient overexpression of ICER; (3) similar results were obtained in 8-Br-cAMP-stimulated R2C cells, a Leydig tumor cell line routinely used for the study of P450(AROM) promoter activity; (4) both ICER mRNA levels and P450(AROM) promoter-driven luciferase activity were elevated 6 and 12 h after stimulation of R2C cells with 8-Br-cAMP and were decreased 24 and 48 h later; (5) in an R2C polyclonal line overexpressing ICER, the promoter activity at early stages of stimulation was completely attenuated, while 24 and 48 h downregulation was prevented in another R2C line stably transfected with an antisense ICER construct. These results suggest that ICER represses CYP19 ovarian promoter and that LH-induced expression of ICER may serve to downregulate P450(AROM) transcription in granulosa cells during luteinization.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Endocrinologyen_US
dc.sourceJournal of Endocrinology [ISSN 0022-0795], v. 179, p. 417-425en_US
dc.subject32 Ciencias médicasen_US
dc.subject320502 Endocrinologíaen_US
dc.subject.otherLong-Term Desensitizationen_US
dc.subject.otherElement-Binding Proteinen_US
dc.subject.otherSubunit Gene-Expressionen_US
dc.subject.otherR2C Leydig-Cellsen_US
dc.subject.otherGranulosa-Cellsen_US
dc.subject.otherCyclic Adenosine-3',5'-Monophosphateen_US
dc.subject.otherDna-Bindingen_US
dc.subject.otherAromatase Promoteren_US
dc.subject.otherTranscriptional Activationen_US
dc.subject.otherConstitutive Expressionen_US
dc.titleThe inducible isoform of CREM (inducible cAMP early repressor, ICER) is a repressor of CYP19 rat ovarian promoteren_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1677/joe.0.1790417en_US
dc.identifier.scopus0347917307-
dc.identifier.isi000187930200012-
dcterms.isPartOfJournal Of Endocrinology-
dcterms.sourceJournal Of Endocrinology[ISSN 0022-0795],v. 179 (3), p. 417-425-
dc.contributor.authorscopusid7005232305-
dc.contributor.authorscopusid6507425244-
dc.contributor.authorscopusid7102922509-
dc.contributor.authorscopusid57211220417-
dc.contributor.authorscopusid8681043500-
dc.contributor.authorscopusid7003526778-
dc.contributor.authorscopusid7003806034-
dc.contributor.authorscopusid7004158812-
dc.description.lastpage425en_US
dc.description.firstpage417en_US
dc.relation.volume179en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000187930200012-
dc.contributor.daisngid1664025-
dc.contributor.daisngid2922182-
dc.contributor.daisngid2446020-
dc.contributor.daisngid128315-
dc.contributor.daisngid329218-
dc.contributor.daisngid31449715-
dc.contributor.daisngid1664323-
dc.contributor.daisngid1127140-
dc.identifier.investigatorRIDK-7776-2014-
dc.identifier.investigatorRIDK-5709-2014-
dc.identifier.investigatorRIDK-9671-2014-
dc.description.numberofpages9en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Morales, V-
dc.contributor.wosstandardWOS:Gonzalez-Robayna, I-
dc.contributor.wosstandardWOS:Hernandez, I-
dc.contributor.wosstandardWOS:Quintana, J-
dc.contributor.wosstandardWOS:Santana, P-
dc.contributor.wosstandardWOS:de Galarreta, CMR-
dc.contributor.wosstandardWOS:Fanjul, LF-
dc.date.coverdateDiciembre 2003en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr3,023-
dc.description.jcrqQ2-
dc.description.scieSCIE-
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0002-7650-4454-
crisitem.author.orcid0000-0001-8937-9034-
crisitem.author.orcid0000-0001-8225-4538-
crisitem.author.orcid0000-0002-4093-2692-
crisitem.author.orcid0009-0000-1982-055X-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameGonzález Robayna, Ignacio Javier-
crisitem.author.fullNameHernández González, Inmaculada Servanda-
crisitem.author.fullNameQuintana Aguiar, José Martín-
crisitem.author.fullNameSantana Delgado, María Del Pino-
crisitem.author.fullNameRuiz De Galarreta Hernandez,C. Manuel-
crisitem.author.fullNameFanjul Rodríguez, Luisa Fernanda-
Colección:Artículos
Adobe PDF (241,66 kB)
Vista resumida

Citas SCOPUSTM   

19
actualizado el 21-abr-2024

Citas de WEB OF SCIENCETM
Citations

17
actualizado el 25-feb-2024

Visitas

56
actualizado el 06-ene-2024

Descargas

4
actualizado el 06-ene-2024

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.