A synonymous mutation of rs1137070 cause the mice Maoa gene transcription and translation to decrease

IF 3.5 3区 医学 Q2 NEUROSCIENCES Frontiers in Molecular Neuroscience Pub Date : 2024-09-18 DOI:10.3389/fnmol.2024.1406708
Kai Xin Li, Lei Fan, Hongjuan Wang, Yushan Tian, Sen Zhang, Qingyuan Hu, Fanglin Liu, Huan Chen, Hongwei Hou
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Abstract

The Monoamine Oxidase-A (MAOA) EcoRV polymorphism (rs1137070) is a unique synonymous mutation (c.1409 T &gt; C) within the MAOA gene, which plays a crucial role in Maoa gene expression and function. This study aimed to explore the relationship between the mouse Maoa rs1137070 genotype and differences in MAOA gene expression. Mice carrying the CC genotype of rs1137070 exhibited a significantly lower Maoa expression level, with an odds ratio of 2.44 compared to the T carriers. Moreover, the wild-type TT genotype of MAOA demonstrated elevated mRNA expression and a longer half-life. We also delved into the significant expression and structural disparities among genotypes. Furthermore, it was evident that different aspartic acid synonymous codons within Maoa influenced both MAOA expression and enzyme activity, highlighting the association between rs1137070 and MAOA. To substantiate these findings, a dual-luciferase reporter assay confirmed that GAC was more efficient than GAT binding. Conversely, the synonymous mutation altered Maoa gene expression in individual mice. An RNA pull-down assay suggested that this alteration could impact the interaction with RNA-binding proteins. In summary, our results illustrate that synonymous mutations can indeed regulate the downregulation of gene expression, leading to changes in MAOA function and their potential association with neurological-related diseases.
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rs1137070的同义突变导致小鼠Maoa基因转录和翻译减少
单胺氧化酶-A(MAOA)EcoRV多态性(rs1137070)是MAOA基因中一个独特的同义突变(c.1409 T&gt;C),在Maoa基因表达和功能中起着至关重要的作用。本研究旨在探讨小鼠 Maoa rs1137070 基因型与 MAOA 基因表达差异之间的关系。携带rs1137070的CC基因型小鼠的Maoa表达水平明显较低,与T型携带者相比,几率为2.44。此外,MAOA 野生型 TT 基因型的 mRNA 表达量升高,半衰期延长。我们还深入研究了不同基因型在表达和结构上的显著差异。此外,Maoa 中不同的天冬氨酸同义密码子显然会影响 MAOA 的表达和酶活性,这凸显了 rs1137070 与 MAOA 之间的关联。为了证实这些发现,双荧光素酶报告实验证实 GAC 比 GAT 结合更有效。相反,同义突变改变了个体小鼠的 Maoa 基因表达。一项 RNA 下拉实验表明,这种改变可能会影响与 RNA 结合蛋白的相互作用。总之,我们的研究结果表明,同义突变确实可以调控基因表达的下调,从而导致 MAOA 功能的改变及其与神经相关疾病的潜在联系。
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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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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