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Ankyrin 3: genetic association with bipolar disorder and relevance to disease pathophysiology

机译:锚蛋白3:与躁郁症的遗传关联以及与疾病病理生理学的关系

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Bipolar disorder (BD) is a multi-factorial disorder caused by genetic and environmental influences. It has a large genetic component, with heritability estimated between 59-93%. Recent genome-wide association studies (GWAS) using large BD patient populations have identified a number of genes with strong statistical evidence for association with susceptibility for BD. Among the most significant and replicated genes is ankyrin 3 (ANK3), a large gene that encodes multiple isoforms of the ankyrin G protein. This article reviews the current evidence for genetic association of ANK3 with BD, followed by a comprehensive overview of the known biology of the ankyrin G protein, focusing on its neural functions and their potential relevance to BD. Ankyrin G is a scaffold protein that is known to have many essential functions in the brain, although the mechanism by which it contributes to BD is unknown. These functions include organizational roles for subcellular domains in neurons including the axon initial segment and nodes of Ranvier, through which ankyrin G orchestrates the localization of key ion channels and GABAergic presynaptic terminals, as well as creating a diffusion barrier that limits transport into the axon and helps define axo-dendritic polarity. Ankyrin G is postulated to have similar structural and organizational roles at synaptic terminals. Finally, ankyrin G is implicated in both neurogenesis and neuroprotection. ANK3 and other BD risk genes participate in some of the same biological pathways and neural processes that highlight several mechanisms by which they may contribute to BD pathophysiology. Biological investigation in cellular and animal model systems will be critical for elucidating the mechanism through which ANK3 confers risk of BD. This knowledge is expected to lead to a better understanding of the brain abnormalities contributing to BD symptoms, and to potentially identify new targets for treatment and intervention approaches.
机译:躁郁症(BD)是由遗传和环境影响引起的多因素疾病。它具有很大的遗传成分,遗传力估计在59-93%之间。最近使用大量BD患者群体进行的全基因组关联研究(GWAS)已鉴定出许多与BD易感性相关的具有强大统计证据的基因。锚蛋白3(ANK3)是最重要和复制最多的基因之一,锚蛋白3是编码锚蛋白G​​蛋白多种同工型的大基因。本文回顾了ANK3与BD遗传关联的当前证据,然后对锚蛋白G蛋白的已知生物学进行了全面概述,重点是其神经功能及其与BD的潜在相关性。锚蛋白G是一种支架蛋白,已知它在大脑中具有许多基本功能,尽管其促成BD的机制尚不清楚。这些功能包括神经元亚细胞结构域的组织作用,包括轴突起始节段和Ranvier的结点,锚蛋白G通过这些功能来协调关键离子通道和GABA能突触前末端的定位,并形成限制进入轴突和轴突运输的扩散屏障。帮助定义轴突树突状极性。假定锚蛋白G在突触末端具有类似的结构和组织作用。最后,锚蛋白G与神经发生和神经保护有关。 ANK3和其他BD风险基因参与某些相同的生物途径和神经过程,这些过程和神经过程突显了几种可能有助于BD病理生理的机制。细胞和动物模型系统中的生物学研究对于阐明ANK3赋予BD风险的机制至关重要。这些知识有望使人们更好地了解导致BD症状的脑部异常,并有可能确定治疗和干预方法的新目标。

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