Jurenka R A, Fabriás G, DeVoe L, Roelofs W L
Department of Entomology, Cornell University, Geneva, NY 14456.
Comp Biochem Physiol Pharmacol Toxicol Endocrinol. 1994 Jul;108(2):153-60. doi: 10.1016/1367-8280(94)90026-4.
Isolated pheromone glands from the redbanded leafroller moth, Argyrotaenia velutinana, were utilized to demonstrate the action of pheromone biosynthesis activating neuropeptide (PBAN) and bursa pheromonotropic peptide plus several other related peptides on pheromone biosynthesis. All peptides belonging to the PBAN family and the bursa peptide stimulated pheromone biosynthesis as measured by pheromone titer and incorporation of radiolabeled acetate. These peptides required the presence of extracellular Ca2+ for expression of full activity and several inorganic Ca2+ channel blockers inhibited the stimulation of pheromone biosynthesis. The Ca2+ ionophore A23187 alone stimulated pheromone biosynthesis as did a cAMP analogue. Stimulation by the cAMP analogue in the absence of extracellular Ca2+ was observed. Maximum pheromone titers were observed in 16 hr gland incubations; however, 2-6 hr incubations were required if pheromone biosynthesis was measured by incorporation of radiolabeled acetate. Radiolabeled glucose incorporation was not increased in the presence of PBAN. These results are discussed in the context of how the pheromone biosynthetic pathway is stimulated by these peptides.
利用从红带卷叶蛾(Argyrotaenia velutinana)分离出的性信息素腺体,来证明性信息素生物合成激活神经肽(PBAN)、囊促性信息素肽以及其他几种相关肽对性信息素生物合成的作用。通过性信息素滴度和放射性标记乙酸盐的掺入量来衡量,所有属于PBAN家族的肽和囊肽都刺激了性信息素的生物合成。这些肽需要细胞外Ca2+的存在才能充分发挥活性,几种无机Ca2+通道阻滞剂抑制了性信息素生物合成的刺激作用。单独的Ca2+离子载体A23187与cAMP类似物一样刺激了性信息素的生物合成。在没有细胞外Ca2+的情况下,观察到了cAMP类似物的刺激作用。在腺体孵育16小时时观察到最大性信息素滴度;然而,如果通过放射性标记乙酸盐的掺入来测量性信息素生物合成,则需要2 - 6小时的孵育。在PBAN存在的情况下,放射性标记葡萄糖的掺入没有增加。将结合这些肽如何刺激性信息素生物合成途径的背景来讨论这些结果。