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TMEM39A基因在多发性硬化症中作用的初步研究

Preliminary Study on the Role of TMEM39A Gene in Multiple Sclerosis.

作者信息

Wagner Marta, Sobczyński Maciej, Bilińska Małgorzata, Pokryszko-Dragan Anna, Cyrul Małgorzata, Kuśnierczyk Piotr, Jasek Monika

机构信息

Department of Clinical Immunology, Laboratory of Immunogenetics and Tissue Immunology, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, ul. Weigla 12, 53-114, Wrocław, Poland.

Department of Genomics, Faculty of Biotechnology, University of Wrocław, ul. Fryderyka Joliot-Curie 14a, 50-383, Wrocław, Poland.

出版信息

J Mol Neurosci. 2017 Jun;62(2):181-187. doi: 10.1007/s12031-017-0921-1. Epub 2017 Apr 25.

Abstract

Genome-wide association studies (GWAS) have identified hundreds of new potential genetic risk loci associated with numerous complex diseases such as multiple sclerosis (MS). Genes which have been discovered by GWAS are now the focus of numerous ongoing studies. The goal of this study was to confirm and understand the potential role of one of such genes-transmembrane protein 39A gene (TMEM39A)-in multiple sclerosis.We showed the difference in TMEM39A messenger RNA (mRNA) expression between MS patients and controls (T  = 5.429; p = 0.0063). In our study, the lower mRNA expression of TMEM39A gene in patients did not correlate with a higher methylation level of the TMEM39A promoter. Moreover, a decreased level of TMEM39A mRNA was associated neither with rs1132200 nor with rs17281647. Additionally, we did not find an association between these two TMEM39A polymorphisms and the risk and progression of multiple sclerosis.Our investigation is the first which indicates that TMEM39A mRNA expression may be associated with the development and/or course of multiple sclerosis.

摘要

全基因组关联研究(GWAS)已经确定了数百个与多种复杂疾病(如多发性硬化症,MS)相关的新的潜在遗传风险位点。通过GWAS发现的基因现在是众多正在进行的研究的重点。本研究的目的是证实并了解此类基因之一——跨膜蛋白39A基因(TMEM39A)——在多发性硬化症中的潜在作用。我们发现MS患者与对照组之间TMEM39A信使核糖核酸(mRNA)表达存在差异(T = 5.429;p = 0.0063)。在我们的研究中,患者中TMEM39A基因较低的mRNA表达与TMEM39A启动子较高的甲基化水平无关。此外,TMEM39A mRNA水平的降低既与rs1132200无关,也与rs17281647无关。此外,我们未发现这两种TMEM39A多态性与多发性硬化症的风险及病程之间存在关联。我们的研究首次表明,TMEM39A mRNA表达可能与多发性硬化症的发生发展和/或病程有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/5486520/5bde288b9626/12031_2017_921_Fig1_HTML.jpg

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