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哮喘患者线粒体tRNA基因的突变分析

Mutational Analysis of Mitochondrial tRNA Genes in Patients with Asthma.

作者信息

Wang Chun Mei, Zhang Xiao Jing, Ma Ying Jun, Li Xia

机构信息

Bright New District Shenzhen City, Guangdong Province People's Hospital, Shenzhen, Guangdong, China.

Dept. of Pathology, Medical College, Shenzhen University, Shenzhen, Guangdong, China.

出版信息

Iran J Public Health. 2017 May;46(5):620-625.

Abstract

BACKGROUND

Mitochondria are autonomous cellular organelles that oversee a variety of functions such as metabolism, energy production, calcium buffering, and cell fate determination. Most recently, mitochondrial dysfunction caused by mitochondrial mutations played important roles in the pathogenesis of asthma. However, the frequency of mitochondrial tRNA mutations in asthma is largely unknown.

METHODS

Overall, 200 patients with asthma and 100 healthy control subjects were recruited between Jan 2015 and Dec 2015 at the Guangming New District People's Hospital, Shenzhen, Guangdong Province, China. We first performed PCR amplification of the mitochondrial tRNA genes and subsequently sequenced the PCR products, and we used the pathogenicity scoring system to evaluate the potential role of these mutations.

RESULTS

Two patients carrying the tRNA G15927A mutation, three patients carrying the tRNA T5655C mutation and one patient carrying the tRNA A14693G mutation, these mutations were absent in healthy controls. Moreover, these mutations located at positions highly conserved between different species, and may cause a failure in mitochondrial tRNA metabolism, consequently result in mitochondrial dysfunction that responsible for asthma. In addition, the pathogenicity scoring system showed that these mutations should be regarded as "pathogenic".

CONCLUSION

Mitochondrial tRNA mutations caused the mitochondrial dysfunction may be involved in the pathogenesis of asthma. Thus, this study provided novel insight into the molecular mechanism underlying mitochondrial tRNA mutations in asthma. Moreover, screening for the mitochondrial tRNA mutations was advised for the diagnosis of patients with asthma.

摘要

背景

线粒体是自主的细胞器,负责多种功能,如新陈代谢、能量产生、钙缓冲和细胞命运决定。最近,由线粒体突变引起的线粒体功能障碍在哮喘发病机制中发挥了重要作用。然而,哮喘中线粒体tRNA突变的频率在很大程度上尚不清楚。

方法

2015年1月至2015年12月期间,在中国广东省深圳市光明新区人民医院招募了200例哮喘患者和100例健康对照者。我们首先对线粒体tRNA基因进行PCR扩增,随后对PCR产物进行测序,并使用致病性评分系统评估这些突变的潜在作用。

结果

两名患者携带tRNA G15927A突变,三名患者携带tRNA T5655C突变,一名患者携带tRNA A14693G突变,健康对照者中不存在这些突变。此外,这些突变位于不同物种间高度保守的位置,可能导致线粒体tRNA代谢失败,进而导致负责哮喘的线粒体功能障碍。此外,致病性评分系统显示这些突变应被视为“致病性的”。

结论

线粒体tRNA突变导致的线粒体功能障碍可能参与哮喘的发病机制。因此,本研究为哮喘中线粒体tRNA突变的分子机制提供了新的见解。此外,建议对哮喘患者进行线粒体tRNA突变筛查以用于诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f5c/5442274/239c1956d697/IJPH-46-620-g001.jpg

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