A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.

In this report, we investigated the pathogenic mechanism underlying the deafness-associated mitochondrial(mt) tRNA(Asp) 7551A > G mutation. The m.7551A > G mutation is localized at a highly conserved nucleotide(A37), adjacent (3') to the anticodon, which is important for the fidelity of codon recognition and stabilization in functional tRNAs. It was anticipated that the m.7551A > G mutation altered the structure and function of mt-tRNA(Asp) The primer extension assay demonstrated that the m.7551A > G mutation created the m(1)G37 modification of mt-tRNA(Asp) Using cybrid cell lines generated by transferring mitochondria from lymphoblastoid cell lines derived from a Chinese family into mitochondrial DNA(mtDNA)-less (ρ(o)) cells, we demonstrated the significant decreases in the efficiency of aminoacylation and steady-state level of mt-tRNA(Asp) in mutant cybrids, compared with control cybrids. A failure in metabolism of mt-tRNA(Asp) caused the variable reductions in mtDNA-encoded polypeptides in mutant cybrids. Impaired mitochondrial translation led to the respiratory phenotype in mutant cybrids. The respiratory deficiency lowed mitochondrial adenosine triphosphate production and increased the production of oxidative reactive species in mutant cybrids. Our data demonstrated that mitochondrial dysfunctions caused by the m.7551A > G mutation are associated with deafness. Our findings may provide new insights into the pathophysiology of maternally transmitted deafness that was manifested by altered nucleotide modification of mitochondrial tRNA. © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

Citation

Meng Wang, Yanyan Peng, Jing Zheng, Binjiao Zheng, Xiaofen Jin, Hao Liu, Yong Wang, Xiaowen Tang, Taosheng Huang, Pingping Jiang, Min-Xin Guan. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. Nucleic acids research. 2016 Aug 17

PMID: 27536005

search → result