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Glycine Receptors Caught between Genome and Proteome – Functional Implications of RNA Editing and Splicing

机译:甘氨酸受体夹在基因组和蛋白质组之间– RNA编辑和剪接的功能含义

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摘要

Information processing in the brain requires a delicate balance between excitation and inhibition. Glycine receptors (GlyR) are involved in inhibitory mechanisms mainly at a synaptic level, but potential novel roles for these receptors recently emerged due to the discovery of posttranscriptional processing. GLR transcripts are edited through enzymatic modification of a single nucleotide leading to amino acid substitution within the neurotransmitter binding domain. RNA editing produces gain-of-function receptors well suited for generation and maintenance of tonic inhibition of neuronal excitability. As neuronal activity deprivation in early stages of development or in epileptic tissue is detrimental to neurons and because RNA editing of GlyR is up-regulated in temporal lobe epilepsy patients with a severe course of disease a pathophysiological role of these receptors emerges. This review contains a state-of-the-art discussion of (patho)physiological implications of GlyR RNA editing.
机译:大脑中的信息处理需要激发与抑制之间的微妙平衡。甘氨酸受体(GlyR)主要在突触水平上参与抑制机制,但由于转录后加工的发现,最近出现了这些受体的潜在新作用。通过对单个核苷酸进行酶促修饰来修饰GLR转录本,从而导致神经递质结合域内的氨基酸置换。 RNA编辑产生功能增强受体,非常适合于产生和维持对神经元兴奋性的强直抑制作用。由于发育早期或癫痫组织中神经元活性的丧失对神经元有害,并且由于GlyR的RNA编辑在患有严重病程的颞叶癫痫患者中上调,因此出现了这些受体的病理生理作用。这篇综述包含了有关GlyR RNA编辑的(病理)生理影响的最新讨论。

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