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线粒体tRNA(苏氨酸)A15951G突变可能与两个中国家系的Leber遗传性视神经病变相关

[The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].

作者信息

Zhang Yu, Zhang Juan-juan, Ji Yan-chun, Zhang Ming-lian, Tong Yi, Zhao Fu-xin, Qu Jia, Zhou Xiang-tian, Guan Min-xin

机构信息

Giuseppe Attardi Institute of Mitochondrial Biomedicine, Wenzhou Medical College, Wenzhou, Zhejiang, People's Republic of China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):501-6. doi: 10.3760/cma.j.issn.1003-9406.2011.05.006.

Abstract

OBJECTIVE

To explore clinical, genetic and molecular features of two Chinese Han families with Leber's hereditary optic neuropathy (LHON).

METHODS

Ophthalmologic examinations revealed variable severity and age-at-onset of visual loss among probands and other matrilineal relatives of both families. The families exhibited extremely low penetrance of visual impairment. The entire mitochondrial genome of two probands was amplified by PCR in 24 overlapping fragments using sets of oligonucleotide primers.

RESULTS

Sequence analysis of complete mitochondrial genome in the pedigrees excluded three common LHON associated mutations G11778A, G3460A and T14484C, but revealed the presence of a known homoplasmic tRNA(Thr) A15951G mutation. It also showed distinct sets of mtDNA polymorphisms belonging to Eastern Asian haplogroup D4b1. The A15951G mutation is located at the extremely conserved nucleotide (conventional position 71) of tRNA(Thr). Thus, this mutation may alter the structure and stability of mitochondrial tRNA(Thr), thereby leading to a failure in the tRNA metabolism and mitochondrial dysfunction, causing visual impairment.

CONCLUSION

The results suggested that the A15951G mutation might be involved in the pathogenesis of Leber's hereditary optic neuropathy in the two families.

摘要

目的

探究两个中国汉族Leber遗传性视神经病变(LHON)家系的临床、遗传和分子特征。

方法

眼科检查显示两个家系的先证者及其他母系亲属的视力丧失严重程度和发病年龄各不相同。这两个家系的视力损害外显率极低。使用寡核苷酸引物组通过聚合酶链反应(PCR)在24个重叠片段中扩增两个先证者的整个线粒体基因组。

结果

家系线粒体基因组全序列分析排除了三个常见的与LHON相关的突变G11778A、G3460A和T14484C,但发现存在一个已知的同质性tRNA(苏氨酸)A15951G突变。还显示出属于东亚单倍群D4b1的不同线粒体DNA多态性组合。A15951G突变位于tRNA(苏氨酸)的高度保守核苷酸(常规位置71)处。因此,该突变可能会改变线粒体tRNA(苏氨酸)的结构和稳定性,从而导致tRNA代谢失败和线粒体功能障碍,引起视力损害。

结论

结果表明,A15951G突变可能参与了这两个家系Leber遗传性视神经病变的发病机制。

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