CLONING AND SEQUENCING OF THE GOLDFISH GROWTH-HORMONE CDNA

Citation
Ss. Mahmoud et al., CLONING AND SEQUENCING OF THE GOLDFISH GROWTH-HORMONE CDNA, General and comparative endocrinology, 101(2), 1996, pp. 139-144
Citations number
30
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
00166480
Volume
101
Issue
2
Year of publication
1996
Pages
139 - 144
Database
ISI
SICI code
0016-6480(1996)101:2<139:CASOTG>2.0.ZU;2-4
Abstract
This study cloned a cDNA encoding the mature goldfish growth hormone ( gGH) using polymerase chain reaction. The nucleotide sequence of the g GH was greater than 90% homologous to that of common carp, silver carp , bighead carp, and grass carp. The amino acid sequence of gGH, determ ined based on the nucleotide sequence of its cDNA, showed more than 93 % homology to that of other mentioned Cyprinid species, 64% to salmon GH, and 32% to human GH. The cloned gGH was found to lack a cysteine ( Cys) residue at position 123 which contrasts with the GH of other Cypr inid species studied to date. The goldfish GH contained only four Cys residues that could be aligned with those of other GHs. This is signif icant from an evolutionary standpoint, suggesting possible divergence among cyprinids. The cloned gGH cDNA was used as a probe in Northern b lotting analysis to investigate the effect of salmon gonadotropin-rele asing hormone (sGnRH) on goldfish GH mRNA production in vivo. The resu lts demonstrate for the first time a strong dose-related stimulation o f GH synthesis by sGnRH in the goldfish pituitary. (C) 1996 Academic P ress, Inc.