Jessika Issa, F. Mbaye, Ly Fatou, A. Diallo, Pape Mbacké Sembène
{"title":"Variations Analysis of Mitochondrial Cytochrome b (MT-CYB) Gene in Malnourished Children from Senegal","authors":"Jessika Issa, F. Mbaye, Ly Fatou, A. Diallo, Pape Mbacké Sembène","doi":"10.33425/2768-0363.1014","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":297300,"journal":{"name":"Pediatrics and Neonatal Medicine","volume":"149 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatrics and Neonatal Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33425/2768-0363.1014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.