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dc.creatorJanjić, Marija
dc.creatorStojilković, Stanko S.
dc.creatorBjelobaba, Ivana
dc.date.accessioned2017-11-23T11:33:55Z
dc.date.available2017-11-23T11:33:55Z
dc.date.issued2017
dc.identifier.issn1664-2392
dc.identifier.urihttp://journal.frontiersin.org/article/10.3389/fendo.2017.00221/full
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/2853
dc.description.abstractThe hypothalamic decapeptide gonadotropin-releasing hormone (GnRH), acting via its receptors (GnRHRs) expressed in pituitary gonadotrophs, represents a critical molecule in control of reproductive functions in all vertebrate species. GnRH-activated receptors regulate synthesis of gonadotropins in a frequency-dependent manner. The number of GnRHRs on the plasma membrane determines the responsiveness of gonadotrophs to GnRH and varies in relation to age, sex, and physiological status. This is achieved by a complex control that operates at transcriptional, translational, and posttranslational levels. This review aims to overview the mechanisms of GnRHR gene (Gnrhr) transcription in mammalian gonadotrophs. In general, Gnrhr exhibits basal and regulated transcription activities. Basal Gnrhr transcription appears to be an intrinsic property of native and immortalized gonadotrophs that secures the presence of a sufficient number GnRHRs to preserve their functionality independently of the status of regulated transcription. On the other hand, regulated transcription modulates GnRHR expression during development, reproductive cycle, and aging. GnRH is crucial for regulated Gnrhr transcription in native gonadotrophs but is ineffective in immortalized gonadotrophs. In rat and mouse, both basal and GnRH-induced Gnrhr transcription rely primarily on the protein kinase C signaling pathway, with subsequent activation of mitogen-activated protein kinases. Continuous GnRH application, after a transient stimulation, shuts offregulated but not basal transcription, suggesting that different branches of this signaling pathway control transcription. Pituitary adenylate cyclase-activating polypeptide, but not activins, contributes to the regulated transcription utilizing the protein kinase A signaling pathway, whereas a mechanisms by which steroid hormones modulate Gnrhr transcription has not been well characterized.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41014/RS//
dc.relationIntramural Research Program of the National Institute of Child Health and Human Development, NIH, Project ZIA HD 000195-22 (SS)
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceFrontiers in Endocrinology
dc.subjectBasal transcription
dc.subjectGonadotrophs
dc.subjectGonadotropin-releasing hormone
dc.subjectGonadotropin-releasing hormone receptor
dc.subjectRegulated transcription
dc.titleIntrinsic and Regulated Gonadotropin-Releasing Hormone Receptor Gene Transcription in Mammalian Pituitary Gonadotrophsen
dc.typearticle
dc.rights.licenseBY
dcterms.abstractЈањић, Марија; Бјелобаба, Ивана; Стојилковић, Станко С.;
dc.rights.holder© 2017 Janjic, Stojilkovic and Bjelobaba.
dc.citation.issueSEP
dc.citation.volume8
dc.identifier.doi10.3389/fendo.2017.00221
dc.identifier.pmid28928715
dc.identifier.scopus2-s2.0-85029220118
dc.identifier.wos000409268900001
dc.citation.apaJanjic, M. M., Stojilkovic, S. S., & Bjelobaba, I. (2017). Intrinsic and Regulated Gonadotropin-Releasing Hormone Receptor Gene Transcription in Mammalian Pituitary Gonadotrophs. Frontiers in Endocrinology, 8(SEP), 221
dc.citation.vancouverJanjic MM, Stojilkovic SS, Bjelobaba I. Intrinsic and Regulated Gonadotropin-Releasing Hormone Receptor Gene Transcription in Mammalian Pituitary Gonadotrophs. Front Endocrinol (Lausanne). 2017;8(SEP):221.
dc.citation.spage221
dc.citation.epage221
dc.type.versionpublishedVersionen
dc.identifier.fulltexthttps://radar.ibiss.bg.ac.rs//bitstream/id/3660/FrontEndocrinolLausanne_2017_8_SEP_221.pdf
dc.citation.rankM22


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