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Endocrinology Vol. 144, No. 6 2461-2472
Copyright © 2003 by The Endocrine Society

Transcription Factors May Frame Aa-nat Gene Expression and Melatonin Synthesis at Night in the Syrian Hamster Pineal Gland

Marie-Laure Garidou, Elena Diaz, Christiane Calgari, Paul Pévet and Valérie Simonneaux

Laboratoire de Neurobiologie des Rythmes (M.-L.G., C.G., P.P., V.S.), Unité Mixte Recherche-Centre National de la Recherche Scientifique-Université Louis Pasteur 7518, F-67000 Strasbourg, France; and Departamento de Biología Funcional (E.D.), Area Fisiología, Facultad de Medicina, Universidad de Oviedo, 33006 Oviedo, Spain

Address all correspondence and requests for reprints to: Valérie Simonneaux, Laboratoire de Neurobiologie des Rythmes, Unité Mixte Recherche-Centre National de la Recherche Scientifique-Université Louis Pasteur 7518, 12, rue de l’Université, F-67000 Strasbourg, France. E-mail: simonneaux{at}neurochem.u-strasbg.fr.

Pineal melatonin synthesis is stimulated at night following an increase in arylalkylamine-N-acetyltransferase (AA-NAT) activity. Depending on the species, two mechanisms of enzyme activation have been described: a cAMP/phospho-cAMP response element-binding protein-dependent stimulation of Aa-nat gene transcription in the rat, presumed to occur in all rodents, or a posttranslational regulation of AA-NAT protein in ongulates. The present data obtained in the Syrian hamster indicate another route of AA-NAT regulation. Elevated nocturnal levels of Aa-nat mRNA were strongly suppressed following light exposure or adrenergic antagonist administration, demonstrating the involvement of norepinephrine in the stimulation of melatonin synthesis. However, administration of adrenergic agonists during the day did not increase Aa-nat mRNA unless a protein synthesis inhibitor was given during the previous night. This indicates that an inhibitory protein, synthesized at night, prevents melatonin synthesis during the day. By contrast, a protein synthesis inhibitor given at the beginning of the night markedly reduced Aa-nat mRNA, suggesting that a stimulatory protein (transcription factor?) is necessary for Aa-nat gene transcription at night. Noteworthy, hamsters raised in long photoperiod were responsive to adrenergic agonist injection only in the first hour after light onset, a response that may be important in this photoperiodic species in which the melatonin peak extends into the morning hours in a short photoperiod.




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