Literature DB >> 25693701

The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population.

Xing Meng1, Hui Pei1, Chao Lan1.   

Abstract

We reported here the possible role of a mitochondrial tRNA mutation: T4353C in clinical expression of essential hypertension in Chinese population. The human mammalian mitochondrial tRNA database was used to analyze the conservation index of this mutation between different species. Moreover, phylogenetic analysis showed that the T4353C mutation belonged to human mitochondrial haplogroup HV, a West Eurasian haplogroup found throughout Western Asia and Eastern European but was infrequent in China. In addition, structural prediction of the T4353C mutation indicated that this transition did not alter the secondary structure of tRNA(Gln). Together, our data indicated that the T4353C mutation occurred infrequent and may not be associated with essential hypertension in Han Chinese population.

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Keywords:  Haplogroup; T4353C mutation; mitochondrial tRNAGln

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Year:  2015        PMID: 25693701     DOI: 10.3109/19401736.2015.1018199

Source DB:  PubMed          Journal:  Mitochondrial DNA A DNA Mapp Seq Anal        ISSN: 2470-1394            Impact factor:   1.514


  1 in total

1.  Novel mitochondrial tRNALeu(UUR) 3261A > g mutation in two pedigrees with essential hypertension.

Authors:  Ye Fu; Pan Jing; Lina Yao; Huajun Wang; Chengjie Zhou
Journal:  Ir J Med Sci       Date:  2022-06-03       Impact factor: 1.568

  1 in total

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