Greenwood M T, Guo Y, Kumar U, Beauséjours S, Hussain S N
Department of Medicine, Royal Victoria Hospital, Montreal, Quebec, Canada.
Biochem Biophys Res Commun. 1997 Sep 18;238(2):617-21. doi: 10.1006/bbrc.1997.7361.
In neuronal cells, nitric oxide (NO) is synthesized by neuronal nitric oxide synthase (nNOS) and performs various functions including neurotransmission, modulation of nociception and long-term potentiation and memory. Recently, a novel 89-amino acid protein, designated PIN, has been shown to interact specifically with nNOS and inhibit nNOS dimerization. In this report, we investigated the distribution and the correlation of PIN with that of nNOS in various brain regions of rats. Amplified PIN cDNA from brain tissues revealed an open reading frame which is identical to that of human PIN. Northern blotting of brain RNA with PIN cDNA produced two transcripts, a major 0.9 kb and a minor 2.5 kb. Expression of PIN cDNA as a fusion protein in E. coli produced a 10 kDa protein which interacted specifically with pure nNOS in an overlay assay. Immunoblotting of rat brain regions with nNOS antibody demonstrated strong expression in the cerebellum, moderate expression in the cerebral cortex, midbrain, medulla and hippocampus with only weak expression in the spinal cord. By comparison, PIN expression was stronger in the cerebral cortex, midbrain, hippocampus and medulla compared with that of cerebellum and spinal cord. We conclude that PIN interacts strongly with nNOS and is constitutively expressed in various brain regions. The dissimilarity between nNOS and PIN expressions in various brain regions may explain the well known differences in NOS activity between these regions. Our results also suggest that PIN may serve other functions other than nNOS inhibition.
在神经元细胞中,一氧化氮(NO)由神经元型一氧化氮合酶(nNOS)合成,并执行多种功能,包括神经传递、伤害感受调节、长时程增强和记忆。最近,一种名为PIN的新型89个氨基酸的蛋白质已被证明可与nNOS特异性相互作用并抑制nNOS二聚化。在本报告中,我们研究了PIN在大鼠不同脑区的分布及其与nNOS分布的相关性。从脑组织中扩增的PIN cDNA显示出一个与人类PIN相同的开放阅读框。用PIN cDNA对脑RNA进行Northern印迹分析产生了两种转录本,一种主要的0.9 kb和一种次要的2.5 kb。PIN cDNA作为融合蛋白在大肠杆菌中表达产生了一种10 kDa的蛋白质,该蛋白质在覆盖分析中与纯nNOS特异性相互作用。用nNOS抗体对大鼠脑区进行免疫印迹分析表明,小脑表达强烈,大脑皮质、中脑、延髓和海马表达中等,脊髓仅表达较弱。相比之下,与小脑和脊髓相比,PIN在大脑皮质、中脑、海马和延髓中的表达更强。我们得出结论,PIN与nNOS强烈相互作用,并在不同脑区组成性表达。不同脑区中nNOS和PIN表达的差异可能解释了这些区域之间众所周知的NOS活性差异。我们的结果还表明,PIN可能具有除抑制nNOS之外的其他功能。