The Relationship between Alpha-Synuclein (SNCA) Gene Polymorphisms and Development Risk of Parkinson’s Disease

Nevra Alkanli, A. Ay
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引用次数: 4

Abstract

Parkinson’s disease (PD) is a neurodegenerative disorder affecting the motor system and occurring in the central nervous system. One of the symptoms of PD is accumulation of Lewy bodies and Lewy neurites. The alpha-synuclein (SNCA) gene is part of the protein complex called Lewy body. The SNCA gene encoding a presynaptic protein product is thought to play a role in PD-related important pathways. It is suggested that there is a relationship between the risk of PD development and SNCA levels, and it is suggested that SNCA level is an important marker in PD diagnosis. Various polymorphisms have been identified in the 5 ′ and/or 3 ′ UTR regions of the SNCA gene, and as a result of these polymorphisms, changes occur in the binding of transcription factors. The identification of the roles of SNCA gene polymorphisms in PD development may enable the development of new methods for the treatment of PD.
α -突触核蛋白(SNCA)基因多态性与帕金森病发展风险的关系
帕金森病(PD)是一种影响运动系统和发生在中枢神经系统的神经退行性疾病。PD的症状之一是路易小体和路易神经突的积聚。α -突触核蛋白(SNCA)基因是称为路易体的蛋白质复合物的一部分。编码突触前蛋白产物的SNCA基因被认为在pd相关的重要通路中发挥作用。提示SNCA水平与PD发生风险有一定关系,SNCA水平是PD诊断的重要指标。在SNCA基因的5 '和/或3 ' UTR区域发现了各种多态性,并且由于这些多态性,转录因子的结合发生了变化。SNCA基因多态性在PD发展中的作用的鉴定可能有助于开发治疗PD的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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