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BOR - Papers in Press, published online ahead of print May 26, 2004.
Biol Reprod 2004, 10.1095/biolreprod.104.028019
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BIOLOGY OF REPRODUCTION 71, 1026–1035 (2004)
DOI: 10.1095/biolreprod.104.028019
© 2004 by the Society for the Study of Reproduction, Inc.


Neuroendocrinology

Developmental Expression of Three Forms of Gonadotropin-Releasing Hormone and Ontogeny of the Hypothalamic-Pituitary-Gonadal Axis in Gilthead Seabream (Sparus aurata)1

Ten-Tsao Wong3, Yoav Gothilf4, Nilli Zmora3, Katherine E. Kight3, Iris Meiri5, Abigail Elizur6, and Yonathan Zohar2,3

Center of Marine Biotechnology,3 University of Maryland Biotechnology Institute, Baltimore, Maryland 21202 Department of Zoology,4 George S. Wise Faculty of Life Sciences, Tel-Aviv University, Israel Israel Oceanographic and Limnological Research,5 National Center for Mariculture, Eilat, Israel Bribie Island Aquaculture Research Center,6 Queensland Department of Primary Industries, Woorim, Queensland, Australia

To address the complexity of the origin of the GnRH system in perciforms, we investigated the ontogenic expression of three GnRHs in gilthead seabream. Using in situ hybridization, chicken (c) GnRH-II mRNA-expressing cells were detected in the hindbrain at 1.5 days postfertilization (DPF) and in the midbrain at 2 DPF and thereafter; the hindbrain signals became undetectable after 10 DPF. Salmon (s) GnRH mRNA-expressing cells were first seen in the olfactory placode at 3 DPF, started caudal migration at 14 DPF, and reached the preoptic areas at 59 DPF. Seabream (sb) GnRH mRNA-expressing cells were first detected in the terminal nerve ganglion cells (TNgc), ventral part of the ventral telencephalon, nucleus preopticus parvocellularis, and thalamus at 39 DPF, and extended to the nucleus preopticus magnocellularis at 43 DPF, ventrolateral hypothalamus at 51 DPF, and nucleus lateralis tuberis and posterior tuberculum at 59 DPF. Coexpression of sbGnRH and sGnRH transcripts was found in the TNgc. Using real-time fluorescence-based quantitative polymerase chain reaction, transcript levels of cGnRH-II and sGnRH were first detected at 1 and 1.5 DPF, respectively, and increased and remained high thereafter. Transcript levels of sbGnRH remained low after first detection at 1 DPF. Furthermore, these GnRH expression profiles were correlated with the expression profiles of reproduction-related genes in which at least four concomitant increases of GnRH, GnRH receptor, gonadotropin, gonadotropin receptor, and Vasa transcripts were found at 5, 8, 14, and 28 DPF. Our data provide an expanded view of the ontogeny of the GnRH system and reproductive axis in perciforms.

1 Supported by US-Israel Bi-national Agricultural Research and Development (BARD) Foundation grant 3428-03 (Y.G. and Y.Z.); Maryland Sea Grant Fellowship (T.-T.W.); and MDSG award NA46RG0091 (Y.Z.). This is contribution number 04-621 from the Center of Marine Biotechnology, University of Maryland Biotechnology Institute.

2 Correspondence: Yonathan Zohar, 701 East Pratt Street, Baltimore, MD 21202. FAX: 410 234 8896; zohar{at}umbi.umd.edu




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