Galanin gene expression and effects of its knock-down on the development of the nervous system in larval zebrafish

Authors

  • P. Podlasz,

    1. Neuroscience Center and Institute of Biomedicine, Anatomy, University of Helsinki, FIN-00014 Helsinki, Finland
    2. Department of Animal Anatomy, Faculty of Veterinary Medicine, University of Warmia and Mazury, 10-719 Olsztyn, Poland
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  • V. Sallinen,

    1. Neuroscience Center and Institute of Biomedicine, Anatomy, University of Helsinki, FIN-00014 Helsinki, Finland
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  • Y.-C. Chen,

    1. Neuroscience Center and Institute of Biomedicine, Anatomy, University of Helsinki, FIN-00014 Helsinki, Finland
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  • H. Kudo,

    1. Neuroscience Center and Institute of Biomedicine, Anatomy, University of Helsinki, FIN-00014 Helsinki, Finland
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  • N. Fedorowska,

    1. Department of Animal Anatomy, Faculty of Veterinary Medicine, University of Warmia and Mazury, 10-719 Olsztyn, Poland
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  • P. Panula

    Corresponding author
    1. Neuroscience Center and Institute of Biomedicine, Anatomy, University of Helsinki, FIN-00014 Helsinki, Finland
    • Neuroscience Center and Institute of Biomedicine, Anatomy, P.O. Box 63 (Haartmaninkatu 8), University of Helsinki, FIN-00014 Helsinki, Finland
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Abstract

Despite the known importance of galanin in the nervous system of vertebrates, the galanin gene structure and expression and the consequences of galanin deficiency in developing zebrafish are unknown. We cloned the galanin gene and analyzed its expression by using in situ hybridization, PCR, and immunocytochemistry throughout the early development of zebrafish until the end of the first week of life. The single zebrafish galanin gene encoded for a single amidated galanin peptide and a galanin message-associated peptide. Two forms resulting from alternative processing were identified. Galanin mRNA was maternally expressed and found in developing fish throughout early development. In situ hybridization showed the first positive neurons in three groups in the brain at 28 hours postfertilization. At 2 days postfertilization, three prosencephalic neuron groups were seen in the preoptic area and in rostral and caudal periventricular hypothalamus. In addition, two other groups of weakly stained neurons were visible, one in the midbrain and another in the hindbrain. Translation inhibition of galanin mRNA with morpholino oligonucleotides caused complete disappearance of galanin immunoreactivity in the brain until 7 dpf and did not induce known cascades of nonspecific pathways or morphological abnormalities. A minor disturbance of sensory ganglia was found. Galanin knockdown did not alter the expression of tyrosine hydroxylases 1 and 2, choline acetyltransferase, histidine decarboxylase, or orexin mRNA. The results suggest that galanin does not regulate the development of these key markers of specific neurons, although galanin-expressing fibers were in a close spatial proximity to several neurons of these neuronal populations. J. Comp. Neurol. 520:3846–3862, 2012. © 2012 Wiley Periodicals, Inc.

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