Differential Neuroendocrine Expression of Multiple Brain-Derived Neurotrophic Factor Transcripts

• Published in: Endocrinology (Philadelphia) 2009-03, Vol.150 (3), p.1361-1368
• Main Authors: Kidane, Adhanet H, Heinrich, Gerhard, Dirks, Ron P. H, de Ruyck, Brechje A, Lubsen, Nicolette H, Roubos, Eric W, Jenks, Bruce G
• Format: Article
• Language: English
• Subjects: Adaptation; Adaptation, Physiological - genetics; Animals; Base Sequence; Biological and medical sciences; Biosynthesis; Brain; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Brain-Derived Neurotrophic Factor - metabolism; Cloning, Molecular; Color; Environmental factors; Exons; Fundamental and applied biological sciences. Psychology; Gene expression; Gene Expression Regulation; Molecular Sequence Data; Neuroendocrine Cells - metabolism; Open reading frames; Organ Specificity - genetics; Pro-Opiomelanocortin - genetics; Proopiomelanocortin; Protein biosynthesis; Protein Biosynthesis - physiology; Proteins; Proto-Oncogene Proteins c-fos - genetics; Regulatory Elements, Transcriptional - genetics; RNA, Messenger - metabolism; Time Factors; Translation; Vertebrates: endocrinology; Xenopus; Xenopus laevis - genetics
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2008-0993

Brain-derived neurotrophic factor (BDNF) is a neurotrophin with important growth-promoting properties. We report here the first characterization of a BDNF gene in an amphibian, Xenopus laevis, and demonstrate that environmental factors can activate this gene in a promoter-specific fashion. The Xenopus BDNF gene contains six promoter-specific 5′-exons and one 3′-protein-encoding exon. We examined the expression of promoter-specific transcripts in Xenopus neuroendocrine melanotrope cells. These cells make a good model to study how environmental factors control gene expression. In animals placed on a black background melanotrope cells more actively produce and release αMSH than in animals on a white background. BDNF is cosequestered and coreleased with αMSH and stimulates biosynthesis of proopiomelanocortin (POMC), the precursor protein for αMSH. Our analysis of the expression of the BDNF transcripts revealed that there is differential use of some BDNF promoters in melanotrope cells, depending on the adaptation state of the frog. During black-background adaptation, stimulation of expression of BDNF transcript IV preceded that of the POMC transcript, suggesting the BDNF gene is an effector gene for POMC expression. The possible mechanisms regulating expression of the various transcripts are discussed on the basis of the potential calcium- and cAMP-responsive elements in the promoter region of exon IV. Finally, we show that the upstream open reading frames of BDNF transcripts I and IV markedly decrease BDNF translation efficiency, giving the first indication for a functional role of untranslated BDNF exons. We show promoter-specific expression of BDNF transcripts in neuroendocrine melanotrope cells and provide evidence that upstream open reading frames of BDNF transcripts decrease translation efficiency.