Characterization of Two Melanin-Concentrating Hormone Genes in Zebrafish Reveals Evolutionary and Physiological Links with the Mammalian MCH System

被引:76
作者
Berman, Jennifer R.
Skariah, Gemini
Maro, Geraldine S. [2 ]
Mignot, Emmanuel
Mourrain, Philippe [1 ,3 ]
机构
[1] Stanford Univ, Ctr Narcolepsy, Dept Psychiat & Behav Sci, Palo Alto, CA 94304 USA
[2] Stanford Univ, Howard Hughes Med Inst, Dept Biol & Pathol, Palo Alto, CA 94305 USA
[3] Ecole Normale Super, INSERM, U784, F-75005 Paris, France
基金
美国国家卫生研究院;
关键词
melanin-concentrating hormone; MCH1; MCH2; pigmentation; feeding; zebrafish; PROTEIN-COUPLED RECEPTOR; DIET-INDUCED OBESITY; TELEOST FISH; IMMUNOCYTOCHEMICAL IDENTIFICATION; CARASSIUS-AURATUS; HYPOCRETIN OREXIN; GENOME EVOLUTION; GOLDFISH BRAIN; FOOD-INTAKE; MICE LEADS;
D O I
10.1002/cne.22171
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Melanin-concentrating hormone (MCH) regulates feeding and complex behaviors in mammals and pigmentation in fish. The relationship between fish and mammalian MCH systems is not well understood. Here, we identify and characterize two MCH genes in zebrafish, Pmch1 and Pmch2. Whereas Pmch1 and its corresponding MCH1 peptide resemble MCH found in other fish, the zebrafish Pmch2 gene and MCH2 peptide share genomic structure, synteny, and high peptide sequence homology with mammalian MCH. Zebrafish Pmch genes are expressed in closely associated but non-overlapping neurons within the hypothalamus, and MCH2 neurons send numerous projections to multiple MCH receptor-rich targets with presumed roles in sensory perception, learning and memory, arousal, and homeostatic regulation. Preliminary functional analysis showed that whereas changes in zebrafish Pmch1 expression correlate with pigmentation changes, the number of MCH2-expressing neurons increases in response to chronic food deprivation. These findings demonstrate that zebrafish MCH2 is the putative structural and functional ortholog of mammalian MCH and help elucidate the nature of MCH evolution among vertebrates. J. Comp. Neurol. 517:695-710, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:695 / 710
页数:16
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