Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family

• Published in: Biochemical and biophysical research communications 2008-03, Vol.367 (4), p.906-911
• Main Authors: Li, Zongbin, Liu, Yuqi, Yang, Li, Wang, Shiwen, Guan, Min-Xin
• Format: Article
• Language: English
• Subjects: Adult; China; DNA Mutational Analysis; Female; Genetic Predisposition to Disease - genetics; Heterozygote; Humans; Hypertension - congenital; Hypertension - genetics; Male; Middle Aged; Mitochondria - genetics; Mitochondrial Diseases - congenital; Mitochondrial Diseases - genetics; Mothers; Pedigree; Penetrance; RNA, Transfer - genetics
• ISSN: 1090-2104
• DOI: 10.1016/j.bbrc.2007.12.150

Mutations in mitochondrial DNA have been associated with cardiovascular disease. We report here the clinical, genetic, and molecular characterization of one three-generation Han Chinese family with maternally transmitted hypertension. All matrilineal relatives in this family exhibited the variable degree of hypertension at the age at onset of 36 to 56 years old. Sequence analysis of the complete mitochondrial DNA in this pedigree revealed the presence of the known hypertension-associated tRNA(Ile) A4295G mutation and 33 other variants, belonging to the Asian haplogroup D4j. The A4295G mutation, which is extraordinarily conserved from bacteria to human mitochondria, is located at immediately 3' end to the anticodon, corresponding to conventional position 37 of tRNA(Ile). The occurrence of the A4295G mutation in several genetically unrelated pedigrees affected by cardiovascular disease but the absence of 242 Chinese controls strongly indicates that this mutation is involved in the pathogenesis of cardiovascular disease. Of other variants, the tRNA(Glu) A14693G and ND1 G11696A mutations were implicated to be associated with other mitochondrial disorders. The A14693G mutation, which is a highly conserved nucleoside at the TpsiC-loop of tRNA(Glu), has been implicated to be important for tRNA structure and function. Furthermore, the ND4 G11696A mutation was associated with Leber's hereditary optic neuropathy. Therefore, the combination of the A4295G mutation in the tRNA(Ile) gene with the ND4 G11696A mutation and tRNA(Glu) A14693G mutation may contribute to the high penetrance of hypertension in this Chinese family.