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与线粒体tRNA(亮氨酸)(UUR)基因(A3243T)新突变相关的线粒体脑肌病

Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).

作者信息

Shaag A, Saada A, Steinberg A, Navon P, Elpeleg O N

机构信息

Metabolic Disease Unit, Shaare-Zedek Medical Center, Jerusalem, Israel.

出版信息

Biochem Biophys Res Commun. 1997 Apr 28;233(3):637-9. doi: 10.1006/bbrc.1997.6496.

Abstract

We report a new mutation, an A-->T transition at nt 3243 in the mitochondrial tRNA(leu)(UUR) gene, in a 9-year-old girl who presented with muscle weakness of 3 years duration complicated by rapidly progressive encephalopathy. In muscle, the activity of the mitochondrial respiratory chain complexes I, III, and IV was markedly reduced. The mutation, involving a highly conserved base pair in the dihydrouridine loop, was heteroplasmic in muscle (81.4%), skin (69.3%), and blood (13.8%) and was not present in blood of 50 healthy individuals. The mitochondrial 3243 base is a "hot spot" for mutations; an A-->G transition at this position is found in a high proportion in most MELAS patients. Since the A-->T transition creates a new recognition site for the restriction enzyme TspRI, both ApaI and TspRI should be used to exclude a mutation at nt 3243.

摘要

我们报告了一名9岁女孩线粒体tRNA(leu)(UUR)基因第3243位核苷酸处发生的一个新突变,即A→T转换。该女孩有3年肌肉无力病史,并伴有快速进展性脑病。在肌肉中,线粒体呼吸链复合物I、III和IV的活性显著降低。该突变位于二氢尿嘧啶环中一个高度保守的碱基对处,在肌肉(81.4%)、皮肤(69.3%)和血液(13.8%)中为异质性,50名健康个体的血液中未发现该突变。线粒体3243位碱基是突变的“热点”;在大多数线粒体脑肌病伴乳酸血症和卒中样发作(MELAS)患者中,该位置的A→G转换比例很高。由于A→T转换产生了限制性内切酶TspRI的一个新识别位点,因此应同时使用ApaI和TspRI来排除第3243位核苷酸处的突变。

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