Kulesza P, Lee C Y, Watson R D
Department of Biology, University of Alabama at Birmingham 35294.
Gen Comp Endocrinol. 1994 Mar;93(3):448-58. doi: 10.1006/gcen.1994.1049.
The 28-kDa size variant of prothoracicotropic hormone (big PTTH) stimulates ecdysteroidogenesis by prothoracic glands of Manduca sexta. In the present studies, big PTTH stimulated in vitro incorporation of [35S]methionine into proteins of prothoracic glands from Day 7 last instar larvae. In 2-hr incubations, big PTTH elicited an approximately 2-fold increase in total protein-specific activity. The effect appeared to be tissue specific, as big PTTH had no effect on incorporation of label into proteins of control tissue (fat body). Electrophoretic separation of tissue homogenates, followed by autoradiography and densitometric analysis, revealed increased incorporation of radiolabel into numerous glandular proteins. The result suggested that the effect of big PTTH was a general stimulation of protein synthesis, not specific stimulation of a subset of glandular proteins. Big PTTH-stimulated ecdysteroidogenesis was inhibited by cycloheximide, indicating that the increase in protein synthesis is a requisite for enhanced hormone production. Analysis of gland incubation media revealed numerous radiolabeled proteins. The effect of big PTTH on incorporation of [35S]methionine into media proteins was considerably more variable than the effect of big PTTH on tissue incorporation. The result is consistent with the hypothesis that prothoracic glands may release proteins in addition to ecdysteroids.
促前胸腺激素的28 kDa大小变体(大PTTH)刺激烟草天蛾前胸腺的蜕皮甾类生成。在本研究中,大PTTH刺激了来自末龄幼虫第7天的前胸腺蛋白质体外掺入[35S]甲硫氨酸。在2小时的孵育中,大PTTH使总蛋白质比活性增加了约2倍。这种效应似乎具有组织特异性,因为大PTTH对标记物掺入对照组织(脂肪体)蛋白质没有影响。对组织匀浆进行电泳分离,随后进行放射自显影和密度分析,结果显示放射性标记物在许多腺蛋白中的掺入增加。结果表明,大PTTH的作用是对蛋白质合成的普遍刺激,而不是对腺蛋白子集的特异性刺激。环己酰亚胺抑制了大PTTH刺激的蜕皮甾类生成,表明蛋白质合成的增加是激素产生增强的必要条件。对腺体孵育培养基的分析揭示了许多放射性标记的蛋白质。大PTTH对[35S]甲硫氨酸掺入培养基蛋白质的影响比大PTTH对组织掺入的影响变化大得多。该结果与前胸腺除了释放蜕皮甾类外还可能释放蛋白质的假说一致。