Tissue-specific expression atlas of murine mitochondrial tRNAs

被引:11
|
作者
He, Qiufen [1 ,2 ,3 ]
He, Xiao [1 ,2 ,3 ]
Xiao, Yun [3 ]
Zhao, Qiong [3 ]
Ye, Zhenzhen [3 ]
Cui, Limei [3 ]
Chen, Ye [1 ,2 ,3 ,4 ]
Guan, Min-Xin [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Zhejiang Univ, Childrens Hosp, Div Med Genet & Genom, Sch Med, Hangzhou, Zhejiang, Peoples R China
[2] Natl Clin Res Ctr Child Hlth, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Inst Genet, Sch Med, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Zhejiang Prov Key Lab Genet & Dev Disorders, Hangzhou, Zhejiang, Peoples R China
[5] Zhejiang Univ, Ctr Mitochondrial Genet, Key Lab Reprod Genet, Minist Educ PRC, Hangzhou, Zhejiang, Peoples R China
[6] Zhejiang Univ Univ Toronto Joint Inst Genet & Gen, Div Mitochondrial Biomed, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
RIBOSOMAL-RNA; M(1)G37 MODIFICATION; MUTATION; AMINOACYLATION; BIOSYNTHESIS; ORGANIZATION; BIOGENESIS; SEQUENCE; MODEL;
D O I
10.1016/j.jbc.2021.100960
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mammalian mitochondrial tRNA (mt-tRNA) plays a central role in the synthesis of the 13 subunits of the oxidative phosphorylation complex system (OXPHOS). However, many aspects of the context-dependent expression of mt-tRNAs in mammals remain unknown. To investigate the tissue-specific effects of mt-tRNAs, we performed a comprehensive analysis of mitochondrial tRNA expression across five mice tissues (brain, heart, liver, skeletal muscle, and kidney) using Northern blot analysis. Striking differences in the tissue-specific expression of 22 mt-tRNAs were observed, in some cases differing by as much as tenfold from lowest to highest expression levels among these five tissues. Overall, the heart exhibited the highest levels of mt-tRNAs, while the liver displayed markedly lower levels. Variations in the levels of mt-tRNAs showed significant correlations with total mitochondrial DNA (mtDNA) contents in these tissues. However, there were no significant differences observed in the 2-thiouridylation levels of tRNALys, tRNAGlu, and tRNAGln among these tissues. A wide range of aminoacylation levels for 15 mt-tRNAs occurred among these five tissues, with skeletal muscle and kidneys most notably displaying the highest and lowest tRNA aminoacylation levels, respectively. Among these tissues, there was a negative correlation between variations in mt-tRNA aminoacylation levels and corresponding variations in mitochondrial tRNA synthetases (mt-aaRS) expression levels. Furthermore, the variable levels of OXPHOS subunits, as encoded by mtDNA or nuclear genes, may reflect differences in relative functional emphasis for mitochondria in each tissue. Our findings provide new insight into the mechanism of mt-tRNA tissue-specific effects on oxidative phosphorylation.
引用
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页数:10
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