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探索 SVA 插入多态性在中枢神经系统中塑造差异基因表达的作用。

Exploring SVA Insertion Polymorphisms in Shaping Differential Gene Expressions in the Central Nervous System.

机构信息

Perron Institute for Neurological and Translational Science, Perth, WA 6009, Australia.

Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3BX, UK.

出版信息

Biomolecules. 2024 Mar 17;14(3):358. doi: 10.3390/biom14030358.

Abstract

Transposable elements (TEs) are repetitive elements which make up around 45% of the human genome. A class of TEs, known as SINE-VNTR-Alu (SVA), demonstrate the capacity to mobilise throughout the genome, resulting in SVA polymorphisms for their presence or absence within the population. Although studies have previously highlighted the involvement of TEs within neurodegenerative diseases, such as Parkinson's disease and amyotrophic lateral sclerosis (ALS), the exact mechanism has yet to be identified. In this study, we used whole-genome sequencing and RNA sequencing data of ALS patients and healthy controls from the New York Genome Centre ALS Consortium to elucidate the influence of reference SVA elements on gene expressions genome-wide within central nervous system (CNS) tissues. To investigate this, we applied a matrix expression quantitative trait loci analysis and demonstrate that reference SVA insertion polymorphisms can significantly modulate the expression of numerous genes, preferentially in the position and in a tissue-specific manner. We also highlight that SVAs significantly regulate mitochondrial genes as well as genes within the and loci, previously associated within neurodegenerative diseases. In conclusion, this study continues to bring to light the effects of polymorphic SVAs on gene regulation and further highlights the importance of TEs within disease pathology.

摘要

转座元件 (TEs) 是重复元件,约占人类基因组的 45%。一类转座元件,称为 SINE-VNTR-Alu (SVA),表现出在整个基因组中移动的能力,导致其在人群中存在或缺失的 SVA 多态性。尽管先前的研究强调了 TEs 在神经退行性疾病(如帕金森病和肌萎缩侧索硬化症 (ALS))中的作用,但确切的机制尚未确定。在这项研究中,我们使用了来自纽约基因组中心 ALS 联盟的 ALS 患者和健康对照者的全基因组测序和 RNA 测序数据,阐明了参考 SVA 元件对中枢神经系统 (CNS) 组织中全基因组基因表达的影响。为了研究这一点,我们应用了矩阵表达数量性状基因座分析,并表明参考 SVA 插入多态性可以显著调节许多基因的表达,优先在 位置并具有组织特异性。我们还强调,SVAs 显著调节线粒体基因以及先前与神经退行性疾病相关的 和 基因座内的基因。总之,这项研究继续揭示多态性 SVA 对基因调控的影响,并进一步强调 TEs 在疾病发病机制中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/427e/10967846/bf6739ba22ea/biomolecules-14-00358-g001.jpg

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