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首页> 外文期刊>Comparative biochemistry and physiology, Part A. Molecular and integrative physiology >Cloning of the crustacean hyperglycemic hormone and evidence for molt-inhibiting hormone within the central nervous system of the blue crab Portunus pelagicus
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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

机译:蓝蟹Portunus pelagicus中枢神经系统中甲壳类高血糖激素的克隆和抑制蜕皮激素的证据

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The 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.
机译:甲壳类X-器官-窦(XO-SG)复合物控制着蜕皮抑制激素(MIH)的产生,尽管已经假定了MIH的额外表达位点。因此,为探索MIH的表达并区分甲壳类高血糖激素(CHH)超家族和中枢神经系统(CNS)中MIH免疫反应位点(ir),我们克隆了蟹蟹Portunus(Ppel- CHH),并将其与螃蟹CHH I和II型肽进行比较。通过多序列比对和系统发育分析,成熟的Ppel-CHH肽显示出CHH I型和II型肽共有的残基,并且与I型基团具有高度同一性,但Ppel-CHH和Ppel-CHI之间几乎没有同源性MIH(II型肽)。然后,通过此序列鉴定,可以使用MIH抗血清进一步确认通过Western印迹法以及免疫组织化学方法检测到的XH,视神经中的MIH-ir,MIH-ir 9. kDa蛋白在所有神经器官中的身份和存在。食管上神经节的神经元簇17,腹神经索和胸神经节的细胞簇22。在中枢神经系统中如此多样的位点中以及在XO-SG外部,MIH蛋白的存在提出了有关已建立的MIH作用方式的新问题。

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