Duve H, Thorpe A, Scott A G, Johnsen A H, Rehfeld J F, Hines E, East P D
School of Biological Sciences, Queen Mary & Westfield College, University of London, England.
Eur J Biochem. 1995 Sep 1;232(2):633-40. doi: 10.1111/j.1432-1033.1995.tb20854.x.
The nonapeptide, Phe-Asp-Asp-Tyr(SO3)-Gly-His-Met-Arg-Phe-NH2 was isolated from heads of the blowfly Calliphora vomitoria. Designated callisulfakinin I, the peptide is identical to the earlier known drosulfakinin I of Drosophila melanogaster and to neosulfakinin I of Neobellieria bullata. It belongs to the sulfakinin family, all known members of which (from flies, cockroaches and locusts) have the C-terminal heptapeptide sequence Asp-Tyr(SO3)-Gly-His-Met-Arg-Phe-NH2. The callisulfakinin gene of C. vomitoria was cloned and sequenced. In addition to callisulfakinin I, the DNA revealed a coding sequence for the putative tetradecapeptide. Gly-Gly-Glu-Glu-Gln-Phe-Asp-Asp-Tyr-Gly-His- Met-Arg-Phe-NH2, callisulfakinin II. However, this peptide was not identified in the fly head extracts. Confocal laser scanning immunocytochemical studies with antisera raised against the synthetic undecapeptide C-terminal fragment of drosulfakinin II from D. melanogaster, Asp-Gln-Phe-Asp-Asp-Tyr(SO3)- Gly-His-Met-Arg-Phe-NH2, revealed only four pairs of sulfakinin neurones in the brain of C. vomitoria and no others anywhere else in the neural, endocrine or gut tissues. In situ hybridisation studies with a digoxigenin-labelled sulfakinin gene probe (from the blowfly Lucilia cuprina) also revealed only four pairs of neurones in the brain. The perikarya of two pairs of cells are situated medially in the caudo-dorsal region, close to the roots of the ocellar nerve. The other perikarya are slightly more posterior and lateral. Although it has been suggested by several authors that the insect sulfakinins are homologous to the vertebrate peptides gastrin and cholecystokinin, such arguments (based essentially on C-terminal structural similarities) do not take account of important differences in the C-terminal tetrapeptide. His-Met-Arg-Phe-NH2 in the sulfakinins, compared with Trp-Met-Asp-Phe-NH2 in gastrin and cholecystokinin. Furthermore, whereas the sulfakinin neurons of C. vomitoria are small in number and have a very specialised location, a greater number of cells throughout the nervous system react positively to gastrin/cholecystokinin antisera. Chromatographic profiles of the present study also revealed peaks of gastrin/cholecystokinin-immunoreactive material separate from the sulfakinin peptides. This evidence suggests that the insect and vertebrate peptides may not necessarily be homologous.
九肽苯丙氨酸 - 天冬氨酸 - 天冬氨酸 - 酪氨酸(磺酸基) - 甘氨酸 - 组氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 氨基从绿头苍蝇(丽蝇)头部中分离出来。该肽被命名为callisulfakinin I,与先前已知的黑腹果蝇的drosulfakinin I以及新蜂蝇的neosulfakinin I相同。它属于速激肽家族,该家族所有已知成员(来自苍蝇、蟑螂和蝗虫)都具有C末端七肽序列天冬氨酸 - 酪氨酸(磺酸基) - 甘氨酸 - 组氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 氨基。克隆并测序了丽蝇的callisulfakinin基因。除了callisulfakinin I外,该DNA还揭示了假定的十四肽甘氨酸 - 甘氨酸 - 谷氨酸 - 谷氨酸 - 谷氨酰胺 - 苯丙氨酸 - 天冬氨酸 - 天冬氨酸 - 酪氨酸 - 甘氨酸 - 组氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 氨基(callisulfakinin II)的编码序列。然而,在苍蝇头部提取物中未鉴定出这种肽。用针对来自黑腹果蝇的drosulfakinin II的合成十一肽C末端片段天冬氨酸 - 谷氨酰胺 - 苯丙氨酸 - 天冬氨酸 - 天冬氨酸 - 酪氨酸(磺酸基) - 甘氨酸 - 组氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 氨基制备的抗血清进行共聚焦激光扫描免疫细胞化学研究,结果显示在丽蝇大脑中仅发现四对速激肽神经元,在神经、内分泌或肠道组织的其他任何部位均未发现其他神经元。用洋地黄毒苷标记的速激肽基因探针(来自绿蝇)进行的原位杂交研究也仅在大脑中发现四对神经元。两对细胞的胞体位于尾背区域的内侧,靠近单眼神经的根部。其他胞体位置稍靠后且更偏外侧。尽管几位作者认为昆虫速激肽与脊椎动物的肽胃泌素和胆囊收缩素是同源的,但这种观点(主要基于C末端结构相似性)没有考虑到C末端四肽的重要差异。速激肽中的组氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 氨基与胃泌素和胆囊收缩素中的色氨酸 - 甲硫氨酸 - 天冬氨酸 - 苯丙氨酸 - 氨基相比。此外,虽然丽蝇的速激肽神经元数量少且位置非常特殊,但整个神经系统中有更多细胞对胃泌素/胆囊收缩素抗血清呈阳性反应。本研究的色谱图还显示了与速激肽肽分开的胃泌素/胆囊收缩素免疫反应性物质的峰。这一证据表明昆虫和脊椎动物的肽不一定是同源的。