Five Crustacean Hyperglycemic Family Hormones of Penaeus monodon: Complementary DNA Sequence and Identification in Single Sinus Glands by Electrospray Ionization-Fourier Transform Mass Spectrometry

• Published in: Marine biotechnology (New York, N.Y.) N.Y.), 2000-01, Vol.2 (1), p.80-91
• Main Authors: Davey, ML, Hall, MR, Willis, RH, Oliver, RW, Thurn, MJ, Wilson, KJ
• Format: Article
• Language: English
• Subjects: Aquatic crustaceans; Bridges; Complementary DNA; Crustaceans; Deoxyribonucleic acid; DNA; DNA libraries; Eyestalks; Fourier transforms; Freshwater crustaceans; Genes; Glands; Homarus americanus; Hormones; Hyperglycemia; Ionization; Ions; Marine; Marine crustaceans; Mass spectrometry; Mass spectroscopy; Molt-inhibiting hormone; Molting; Neuropeptides; Nucleotide sequence; Penaeus monodon; Peptides; Proteins; Scientific imaging; Sequencing; Sinus; Sinus gland; sinus glands; Sinuses; Spectroscopy
• ISSN: 1436-2228; 1436-2236
• DOI: 10.1007/s101269900011

Five novel neuropeptides, designated Pm-sgp-I to -V, of the crustacean hyperglycemic hormone (CHH) family have been identified from the giant tiger prawn Penaeus monodon by isolation of the preprohormone genes from an eyestalk complementary DNA library. On the basis of sequence similarity, the encoded peptides have been classified as CHH-like type I hormones, which include all known CHHs and the molt-inhibiting hormone (MIH) of the lobster Homarus americanus. Consistent with CHH type I preprohormones, the Pm-sgp precursors include a signal peptide, a CHH precursor-related peptide (CPRP), and the CHH-like hormone. Analysis by electrospray ionization-Fourier transform mass spectrometry enabled the neuropeptide complement of individual sinus glands to be resolved. It also confirmed the presence of the five Pm-sgp neuropeptides within the sinus gland of an individual animal, in that the masses observed were consistent with those predicted from the gene sequence of the Pm-sgps after posttranslational modification. These modifications included cleavage of the signal peptide and precursor protein, carboxy-terminal amidation, and formation of three disulfide bridges. Analysis of crude extracts of single sinus glands from different animals revealed variation in neuropeptide content and will provide a tool for determining whether the content varies as a function of the physiological state of the animal.