A Study of Association of the MIR137 VNTR rs58335419 with Schizophrenia

IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Russian Journal of Genetics Pub Date : 2024-03-11 DOI:10.1134/s102279542402008x
G. I. Korovaitseva, I. V. Oleichik, T. V. Lezheiko, V. E. Golimbet
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Abstract

The MIR137 gene encodes microRNA-137 (miR-137), which is a brain-enriched miR that is highly expressed in various brain regions. miR-137 has been identified as a modulator of processes involved in the pathogenesis of neuropsychiatric disorders. Functional polymorphism of variable number of tandem repeats (VNTR) rs58335419 was found in the regulatory region of the MIR137 gene. It is associated with a change in the expression of miR-137 and, as a result, with an increased risk of developing psychopathologies, including schizophrenia. In this study, we for the first time have analyzed the distribution of frequencies of alleles and genotypes of MIR137 VNTR in a large sample from the Russian population. The association of VNTR with the risk of schizophrenia has been studied. It was found that the presence of VNTR alleles with more than three repeats, as well as a genotype homozygous for such alleles, is associated with an increased risk of developing schizophrenia (OR = 1.4, 95% CI: 1.01–1.95).

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MIR137 VNTR rs58335419 与精神分裂症的关联研究
摘要 MIR137基因编码microRNA-137(miR-137),miR-137是一种脑丰富miR,在不同脑区高度表达。在 MIR137 基因的调节区发现了可变串联重复序列(VNTR)rs58335419 的功能多态性。它与 miR-137 的表达变化有关,因此增加了患精神疾病(包括精神分裂症)的风险。在这项研究中,我们首次分析了俄罗斯人口大样本中 MIR137 VNTR 等位基因和基因型的频率分布。我们还研究了 VNTR 与精神分裂症风险的关系。研究发现,存在三个以上重复的 VNTR 等位基因以及此类等位基因的同源基因型与精神分裂症发病风险的增加有关(OR = 1.4,95% CI:1.01-1.95)。
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来源期刊
Russian Journal of Genetics
Russian Journal of Genetics 生物-遗传学
CiteScore
1.00
自引率
33.30%
发文量
126
审稿时长
1 months
期刊介绍: Russian Journal of Genetics is a journal intended to make significant contribution to the development of genetics. The journal publishes reviews and experimental papers in the areas of theoretical and applied genetics. It presents fundamental research on genetic processes at molecular, cell, organism, and population levels, including problems of the conservation and rational management of genetic resources and the functional genomics, evolutionary genomics and medical genetics.
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