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Serotonin induces selective cleavage of the PKA RI subunit but not RII subunit in Aplysia neurons

机译:5-羟色胺诱导海鸟神经元中PKA RI亚基的选择性切割而不诱导RII亚基的切割

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摘要

PKA type I and type II are activated in Aplysia neurons by stimulation with serotonin (5-HT), which causes long-term facilitation (LTF). The proteolysis of the regulatory subunit (R) is thought important for the persistent activation of PKA, which is necessary to produce LTF. In this study, we report that the type I regulatory subunit (RI) and type II regulatory subunit (RII) are differentially regulated by proteolytic cleavage. RI, but not RII, was selectively cleaved after 5-HT treatment for 2 h in Aplysia neurons. Interestingly, the proteasome inhibitor MG132 inhibited the cleavage of RI caused by 5-HT treatment in Aplysia neuron. Besides extracts from Aplysia ganglia treated with 5-HT cleaved 35S-labeled RI synthesized in vitro, but not 35S-labeled RII. This suggests that 5-HT induces the activation state of RI-specific proteolytic cleavage.
机译:PKA I型和II型在海床神经元中通过5-羟色胺(5-HT)刺激而激活,这会引起长期促进(LTF)。人们认为,调节性亚基(R)的蛋白水解对于PKA的持续活化很重要,而PKA的持续活化是产生LTF所必需的。在这项研究中,我们报告说I型调节亚基(RI)和II型调节亚基(RII)通过蛋白水解裂解被不同地调节。在海兔神经元中进行5-HT处理2小时后,选择性裂解RI,而不裂解RII。有趣的是,蛋白酶体抑制剂MG132抑制了海鸟神经元中5-HT处理引起的RI裂解。除了用5-HT裂解的 35 S标记的RI处理的神经节提取物外,还没有 35 S标记的RII的体外合成。这表明5-HT诱导RI特异性蛋白水解切割的激活状态。

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