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Cloning of the crustacean hyperglycemic hormone and evidence for molt-inhibiting hormone within the central nervous system of the blue crab Portunus pelagicus

dc.contributor.authorMichael J. Stewarten_US
dc.contributor.authorPraphaporn Stewarten_US
dc.contributor.authorMorakot Sroyrayaen_US
dc.contributor.authorNantawan Soonklangen_US
dc.contributor.authorScott F. Cumminsen_US
dc.contributor.authorPeter J. Hannaen_US
dc.contributor.authorWei Duanen_US
dc.contributor.authorPrasert Sobhonen_US
dc.contributor.otherDeakin Universityen_US
dc.contributor.otherUniversity of the Sunshine Coasten_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-19T04:41:55Z
dc.date.available2018-10-19T04:41:55Z
dc.date.issued2013-02-01en_US
dc.description.abstractThe crustacean X-organ-sinus gland (XO-SG) complex controls molt-inhibiting hormone (MIH) production, although extra expression sites for MIH have been postulated. Therefore, to explore the expression of MIH and distinguish between the crustacean hyperglycemic hormone (CHH) superfamily, and MIH immunoreactive sites (ir) in the central nervous system (CNS), we cloned a CHH gene sequence for the crab Portunus pelagicus (Ppel-CHH), and compared it with crab CHH-type I and II peptides. Employing multiple sequence alignments and phylogenic analysis, the mature Ppel-CHH peptide exhibited residues common to both CHH-type I and II peptides, and a high degree of identity to the type-I group, but little homology between Ppel-CHH and Ppel-MIH (a type II peptide). This sequence identification then allowed for the use of MIH antisera to further confirm the identity and existence of a MIH-ir 9. kDa protein in all neural organs tested by Western blotting, and through immunohistochemistry, MIH-ir in the XO, optic nerve, neuronal cluster 17 of the supraesophageal ganglion, the ventral nerve cord, and cell cluster 22 of the thoracic ganglion. The presence of MIH protein within such a diversity of sites in the CNS, and external to the XO-SG, raises new questions concerning the established mode of MIH action. © 2012 Elsevier Inc.en_US
dc.identifier.citationComparative Biochemistry and Physiology - A Molecular and Integrative Physiology. Vol.164, No.2 (2013), 276-290en_US
dc.identifier.doi10.1016/j.cbpa.2012.10.029en_US
dc.identifier.issn15314332en_US
dc.identifier.issn10956433en_US
dc.identifier.other2-s2.0-84870312700en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/31370
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870312700&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleCloning of the crustacean hyperglycemic hormone and evidence for molt-inhibiting hormone within the central nervous system of the blue crab Portunus pelagicusen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870312700&origin=inwarden_US

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