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δ-氨基乙酰丙酸脱水酶(ALAD)基因型频率的种族差异。

Ethnic variation in genotype frequencies of delta-aminolevulinic acid dehydratase (ALAD).

作者信息

Fujihara Junko, Agusa Tetsuro, Yasuda Toshihiro, Soejima Mikiko, Kato Hideaki, Panduro Arturo, Koda Yoshiro, Kimura-Kataoka Kaori, Takeshita Haruo

机构信息

Department of Legal Medicine, Shimane University Faculty of Medicine, 89-1 Enya, Izumo 693-8501, Japan.

出版信息

Toxicol Lett. 2009 Dec 15;191(2-3):236-9. doi: 10.1016/j.toxlet.2009.09.005. Epub 2009 Sep 17.

Abstract

Delta-aminolevulinic acid dehydratase (ALAD) is a cytosolic enzyme in the heme biosynthetic pathway. The ALAD is controlled by two codominant alleles (ALAD1 and ALAD2), which result in a Asn-Lys substitution at amino acid position 59 of the mature enzyme based on a single nucleotide polymorphism (SNP) (G177C) leading three phenotypes (ALAD1-1, ALAD1-2, and ALAD2-2). Previous studies have shown that this polymorphism is related to lead toxicity. There is little evidence showing interethnic differences in the distribution of this polymorphism. We examined the distribution of genetic variants of the ALAD G177C polymorphism in four Asians, three Africans, and three Mexicans. Genomic DNA was extracted from blood or bloodstain, and the genotypes for the ALAD polymorphism were determined by PCR followed by RFLP digestion and gel electrophoresis. We found a notable interethnic disparity in the distribution of ALAD G177C genotypes and alleles. The frequencies of ALAD2 in Asian populations were comparable to those in Caucasians, while Africans had no mutation allele. These findings may help us understand the interethnic disparities in susceptibility to lead toxicity.

摘要

δ-氨基乙酰丙酸脱水酶(ALAD)是血红素生物合成途径中的一种胞质酶。ALAD由两个共显性等位基因(ALAD1和ALAD2)控制,基于单核苷酸多态性(SNP)(G177C),这两个等位基因导致成熟酶的第59位氨基酸发生天冬酰胺-赖氨酸替换,产生三种表型(ALAD1-1、ALAD1-2和ALAD2-2)。先前的研究表明,这种多态性与铅毒性有关。几乎没有证据表明这种多态性的分布存在种族间差异。我们研究了四个亚洲人、三个非洲人和三个墨西哥人中ALAD G177C多态性的基因变异分布。从血液或血迹中提取基因组DNA,通过PCR扩增,随后进行限制性片段长度多态性(RFLP)消化和凝胶电泳来确定ALAD多态性的基因型。我们发现ALAD G177C基因型和等位基因的分布存在显著的种族间差异。亚洲人群中ALAD2的频率与白种人相当,而非洲人没有突变等位基因。这些发现可能有助于我们理解种族间对铅毒性易感性的差异。

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