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Endocrinology, doi:10.1210/en.2008-1435
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Endocrinology Vol. 150, No. 4 1826-1833
Copyright © 2009 by The Endocrine Society

Cloning of Gonadotropin-Releasing Hormone I Complementary DNAs in Songbirds Facilitates Dissection of Mechanisms Mediating Seasonal Changes in Reproduction

T. J. Stevenson, K. S. Lynch, P. Lamba, G. F. Ball1 and D. J. Bernard1

Department of Psychological and Brain Sciences (T.J.S., K.S.L., G.F.B.), The Johns Hopkins University, Baltimore, Maryland 21218; and Department of Pharmacology and Therapeutics (P.L., D.J.B.), McGill University, Montreal, Quebec, Canada H3G 1Y62

Address all correspondence and requests for reprints to: T. J. Stevenson, Department of Psychological and Brain Sciences, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218. E-mail: tsteve13{at}jhu.edu.

Temperate zone animals exhibit seasonal variation in reproductive physiology. In most cases, seasonal changes in reproductive states are regulated by changes in GnRH1 secretion, rather than synthesis, from the preoptic area (POA)/anterior hypothalamus. An important exception occurs in some songbirds that become photorefractory to the stimulatory effects of long days and show profound decreases in brain GnRH1 protein content. Whether this decline reflects changes in gene expression is unknown because of past failures to measure GNRH1 mRNA levels, due in large part to the absence of available GNRH1 gene sequence in this taxon. Here, we report the first cloning of GNRH1 cDNAs in two songbirds: European starlings and zebra finches. Consistent with the size of the prepro-hormone in other avian and non-avian species, the open-reading frames predict proteins of 91 and 92 amino acids, respectively. Whereas the decapeptide in both species is perfectly conserved with chicken GnRH1, the amino acid identity in the signal peptide and GNRH associated peptide subdomains are significantly less well conserved. At the nucleotide level, the starling and zebra finch coding sequences are approximately 88% identical to each other but only approximately 70% identical to chicken GNRH1. In situ hybridization using radiolabeled cRNA probes demonstrated GNRH1 mRNA expression primarily in the POA, consistent with previous studies on the distribution of the GnRH1-immunoreactive cell bodies. Furthermore, we provide evidence for photoperiod-dependent regulation of GNRH1 mRNA in male starlings. Declines in GNRH1 mRNA levels occur in parallel with testicular involution. Thus, photorefractoriness is associated with decreases in GNRH1 gene expression in the medial POA.




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