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鉴定和分析科威特人群中基因座第 6 内含子变异。

Identification and Characterization of Variants in Intron 6 of the Gene Locus among a Sample of the Kuwaiti Population.

机构信息

Department of Biological Sciences, Faculty of Science, Kuwait University, Kuwait City 13060, Kuwait.

Kuwait Medical Genetic Center, Ministry of Health, Kuwait City 70051, Kuwait.

出版信息

Genes (Basel). 2022 Apr 9;13(4):664. doi: 10.3390/genes13040664.

Abstract

Lipoprotein lipase (LPL) is responsible for the hydrolysis of lipoproteins; hence defective LPL is associated with metabolic disorders. Here, we identify certain intronic insertions and deletions (InDels) and single nucleotide polymorphisms (SNPs) in intron 6 of the gene and investigate their associations with different phenotypic characteristics in a cohort of the general Kuwaiti population. Two specific regions of intron 6 of the gene, which contain InDels, were amplified via Sanger sequencing in 729 subjects. Genotypic and allelic frequencies were estimated, and genetic modeling was used to investigate genetic associations of the identified variants with lipid profile, body mass index (BMI), and risk of coronary heart disease (CHD). A total of 16 variants were identified, including 2 InDels, 2 novel SNPs, and 12 known SNPs. The most common variants observed among the population were rs293, rs274, rs295, and rs294. The rs293 "A" insertion showed a significant positive correlation with elevated LDL levels, while rs295 was significantly associated with increased BMI. The rs274 and rs294 variants showed a protective effect of the minor allele with decreased CHD prevalence. These findings shed light on the possible role of intronic variants on metabolic disorders.

摘要

脂蛋白脂肪酶(LPL)负责脂蛋白的水解;因此,有缺陷的 LPL 与代谢紊乱有关。在这里,我们鉴定了 基因第 6 内含子中的某些插入和缺失(InDels)和单核苷酸多态性(SNPs),并在科威特普通人群的队列中研究了它们与不同表型特征的关联。通过对 729 名受试者进行 Sanger 测序,扩增了包含 InDels 的 基因第 6 内含子的两个特定区域。估计了基因型和等位基因频率,并使用遗传建模研究了鉴定出的变体与脂质谱、体重指数(BMI)和冠心病(CHD)风险的遗传关联。共发现 16 种变体,包括 2 种 InDels、2 种新的 SNP 和 12 种已知的 SNP。在人群中观察到的最常见变体是 rs293、rs274、rs295 和 rs294。rs293“A”插入与 LDL 水平升高呈显著正相关,而 rs295 与 BMI 增加显著相关。rs274 和 rs294 变体显示出较小等位基因的保护作用,降低了 CHD 的患病率。这些发现揭示了 内含子变异体在代谢紊乱中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5ab/9024856/f87c2972e125/genes-13-00664-g001.jpg

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