塞内加尔营养不良儿童线粒体细胞色素b (MT-CYB)基因变异分析

Jessika Issa, F. Mbaye, Ly Fatou, A. Diallo, Pape Mbacké Sembène
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引用次数: 0

摘要

儿童营养不良是全世界婴儿发病率和死亡率的一个主要原因,因此也是一个主要的公共卫生问题。营养基因组学研究营养与基因之间的相互作用,包括两个领域:营养遗传学和营养基因组学。因此,营养不良(缺乏或过量)会影响基因表达和基因组稳定性。目的:研究可能与儿童营养不良有关的线粒体细胞色素b (MT-CYB)突变及其遗传多样性。材料和方法:我们通过pcr测序分析了23名营养不良儿童和6名健康儿童的MT-CYB变异性。利用Surveyor Mutation软件进行MT-CYB基因突变的搜索。使用9个预测软件程序(即SIFT, PROVEAN, polyphen2, DEOGEN, SNPs & go, PREDICTSNP, MUTATIONTASTER, PANTHER和FATHMM)来确定突变的功能影响。采用DNAsp Version 5.1001、Harlequin Version 3.1和Mega x软件获取MT-CYB的遗传变异各项参数及遗传分化。结果:在营养不良和健康儿童中共鉴定出24个突变(z评分≥20)。在营养不良儿童中存在的非同义突变中,突变p.N206N/I、p.T336H、p.Y345A、p.T348T/N和p.L357L/V被至少五个预测软件程序预测为致病性。氨基酸Ile, Lys, Arg和Asn在正常和营养不良儿童之间显示出显著差异。T+ a(53.72%)高于C+G(46.28%)。结果表明,单倍型多样性高(1.000+/-0.013),核苷酸多样性低(0.10545+/- 0.00488)。结论:我们的结果使我们能够检测到可能与儿童营养不良有关的MT-CYB基因突变。异亮氨酸(Ile)、天冬酰胺(Asn)和精氨酸(Arg)的减少可能与营养不良的风险有关。这项研究将有助于重新调整对抗营养不良的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variations Analysis of Mitochondrial Cytochrome b (MT-CYB) Gene in Malnourished Children from Senegal
Introduction: Child malnutrition is a major cause of infant morbidity and mortality worldwide and thus a major public health problem. The study of interactions between nutrition and genes— nutritional genomics—encompasses two domains: nutrigenetics and nutrigenomics. Malnutrition (deficiency or excess) can thus affect gene expression and genome stability. Objective: The objective of this work is to investigate mutations of interest of Mitochondrial Cytochrome b (MT-CYB) that may be related to child malnutrition and to study the genetic diversity of MT-CYB. Materials and methods: We analyzed the variability of MT-CYB in 23 malnourished children and six healthy children via PCR-sequencing. The search of mutations in the MT-CYB gene was conducted using Surveyor Mutation software. Nine prediction software programs (i.e., SIFT, PROVEAN, POLYPHEN-2, DEOGEN, SNPs & go, PREDICTSNP, MUTATIONTASTER, PANTHER, and FATHMM) were used to determine the functional impact of mutations. The various parameters of the genetic variety as well as the genetic differentiation of MT-CYB were obtained using DNAsp Version 5.1001, Harlequin Version 3.1 and Mega X. Results: A total of 24 mutations (Z-score ≥ 20) were identified in malnourished and healthy children. Among the non-synonym mutations present in malnourished children, mutations p.N206N/I, p.T336H, p.Y345A, p.T348T/N, and p.L357L/V were predicted pathogenic by at least five predictive software programs. The amino acids Ile, Lys, Arg and Asn demonstrate significant differences between normal and malnourished children. There is a predominance of T+A (53.72%) compared to C+G (46.28%). Our results show high haplotypic diversity (1.000+/-0.013) and low nucleotide diversity (0.10545+/- 0.00488). Conclusion: Our results allowed us to detect mutations in the MT-CYB gene that could be linked to childhood malnutrition. A decrease in isoleucine (Ile), asparagine (Asn), and arginine (Arg) may be correlated with the risk of malnutrition. This study will allow to readjust the strategies to fight against malnutrition.
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