非综合征性唇裂rs880810、rss545793、rs80094639和rs13251901单核苷酸多态性的遗传分析:病例-父母三人组研究

IF 1.2 Q4 GENETICS & HEREDITY Global Medical Genetics Pub Date : 2023-01-01 DOI:10.1055/s-0043-1764399
Mahamad Irfanulla Khan, Prashanth Cs, N Srinath, Praveen K Neela, Mohammed K Mohiuddin
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引用次数: 0

摘要

唇裂,包括唇裂(CL),腭裂(CP)和唇腭裂(CLP),是最常见的先天性面部畸形类型。各种遗传和环境因素在唇腭裂的发生中起着重要作用。几项研究表明,PAX7基因和8q24区域与世界各地不同人群的这些口腔裂有关。然而,目前还没有关于PAX7基因和8q24区域核苷酸变异与印度人群发生非综合征性唇腭裂(NSOC)风险之间可能联系的研究报道。因此,本研究旨在采用病例-亲本三重奏设计,检测PAX7基因8q24区域rs880810、rss545793、rs80094639和rs13251901的单核苷酸多态性(snp)之间可能存在的关联。从CLP中心选择了40个病例-父母三人组。从这些病例及其父母身上分离出基因组DNA。采用MassARRAY技术对rs880810、rss545793、rs80094639和rs13251901进行基因分型。采用PLINK软件进行统计分析。所有snp均经Hardy-Weinberg平衡检验。各基因型snp的p值均不小于0.05,故无统计学意义。因此,PAX7基因的rs880810、rss545793和rs80094639以及8q24区域的rs13251901与印度人群的NSOC无关。
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Genetic Analysis of the Single-Nucleotide Polymorphisms rs880810, rs545793, rs80094639, and rs13251901 in Nonsyndromic Oral Clefts: A Case-Parent Trio Study.

Oral clefts, including cleft lip (CL), cleft palate (CP), and cleft lip and palate (CLP), are the most common types of congenital anomalies of the human face. Various genetic and environmental factors play a role in developing oral clefts. Several studies have shown the association of the PAX7 gene and the 8q24 region with these oral clefts in different populations worldwide. However, there are no reported studies on the possible connection between the PAX7 gene and the 8q24 region nucleotide variants and the risk of developing nonsyndromic oral clefts (NSOC) in the Indian population. Hence, this study aimed to test the possible association between PAX7 gene single-nucleotide polymorphisms (SNPs) rs880810, rs545793,rs80094639, and rs13251901 of the 8q24 region using a case-parent trio design. Forty case-parent trios were selected from the CLP center. Genomic DNA was isolated from the cases and their parents. The rs880810, rs545793, rs80094639, and rs13251901 were genotyped by the MassARRAY technique. PLINK software was used for statistical analysis. All the SNPs were tested for Hardy-Weinberg equilibrium. No statistical significance was found with any SNPs, as none of the genotyped SNPs showed a p -value of less than 0.05. Hence, the rs880810, rs545793, and rs80094639 of the PAX7 gene, and rs13251901 of the 8q24 region are not associated with NSOC in the Indian population.

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来源期刊
Global Medical Genetics
Global Medical Genetics GENETICS & HEREDITY-
自引率
11.80%
发文量
30
审稿时长
14 weeks
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