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由于红系5-氨基乙酰丙酸合成酶基因突变导致精氨酸170被亮氨酸取代而引起的X连锁铁粒幼细胞贫血。

X-linked sideroblastic anaemia due to a mutation in the erythroid 5-aminolaevulinate synthase gene leading to an arginine170 to leucine substitution.

作者信息

Edgar A J, Vidyatilake H M, Wickramasinghe S N

机构信息

Department of Haematology, Imperial College School of Medicine, London, UK.

出版信息

Eur J Haematol. 1998 Jul;61(1):55-8. doi: 10.1111/j.1600-0609.1998.tb01061.x.

Abstract

DNA sequencing of the coding region of the erythroid 5-aminolaevulinate synthase (ALAS2) cDNA from a male with pyridoxine-responsive sideroblastic anaemia revealed a missense mutation, a G561T transversion in exon 5 of the gene. Previously, the mutation G561A has been shown to be responsible for sideroblastic anaemia in females and thought to be lethal in males (1). The mutation G561T results in the loss of an MspA1-I cutting site. Analysis of MspA1-I restriction enzyme digests of amplified exon 5 genomic DNA from other family members revealed that the proband's mother, aunt and youngest sister, who were not anaemic, were heterozygous carriers of the mutation. The G561T mutation results in an arginine to leucine substitution at amino acid residue 170. This arginine residue is conserved in both the erythroid and housekeeping ALAS in vertebrates as well as in all other known ALAS proteins and is located in a predicted alpha-helix region close to the amino-terminus of the enzymatic region of the protein.

摘要

对一名患有吡哆醇反应性铁粒幼细胞贫血的男性患者的红系5-氨基乙酰丙酸合酶(ALAS2)cDNA编码区进行DNA测序,发现了一个错义突变,即该基因第5外显子中的G561T颠换。此前,已证明突变G561A是女性铁粒幼细胞贫血的病因,且被认为对男性具有致死性(1)。突变G561T导致MspA1-I切割位点缺失。对其他家庭成员扩增的第5外显子基因组DNA进行MspA1-I限制性酶切分析,结果显示先证者的母亲、姨妈和最小的妹妹虽未患贫血,但均为该突变的杂合携带者。G561T突变导致氨基酸残基170处的精氨酸被亮氨酸取代。该精氨酸残基在脊椎动物的红系和管家型ALAS以及所有其他已知的ALAS蛋白中均保守,且位于蛋白质酶促区域氨基末端附近的一个预测α螺旋区域内。

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