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Tissue-specific expression atlas of murine mitochondrial tRNAs
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-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342785/ https://www.ncbi.nlm.nih.gov/pubmed/34265302 http://dx.doi.org/10.1016/j.jbc.2021.100960 |
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author | He, Qiufen He, Xiao Xiao, Yun Zhao, Qiong Ye, Zhenzhen Cui, Limei Chen, Ye Guan, Min-Xin |
author_facet | He, Qiufen He, Xiao Xiao, Yun Zhao, Qiong Ye, Zhenzhen Cui, Limei Chen, Ye Guan, Min-Xin |
author_sort | He, Qiufen |
collection | PubMed |
description | 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 tRNA(Lys), tRNA(Glu), and tRNA(Gln) 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. |
format | Online Article Text |
id | pubmed-8342785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83427852021-08-11 Tissue-specific expression atlas of murine mitochondrial tRNAs He, Qiufen He, Xiao Xiao, Yun Zhao, Qiong Ye, Zhenzhen Cui, Limei Chen, Ye Guan, Min-Xin J Biol Chem Research Article 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 tRNA(Lys), tRNA(Glu), and tRNA(Gln) 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. American Society for Biochemistry and Molecular Biology 2021-07-13 /pmc/articles/PMC8342785/ /pubmed/34265302 http://dx.doi.org/10.1016/j.jbc.2021.100960 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article He, Qiufen He, Xiao Xiao, Yun Zhao, Qiong Ye, Zhenzhen Cui, Limei Chen, Ye Guan, Min-Xin Tissue-specific expression atlas of murine mitochondrial tRNAs |
title | Tissue-specific expression atlas of murine mitochondrial tRNAs |
title_full | Tissue-specific expression atlas of murine mitochondrial tRNAs |
title_fullStr | Tissue-specific expression atlas of murine mitochondrial tRNAs |
title_full_unstemmed | Tissue-specific expression atlas of murine mitochondrial tRNAs |
title_short | Tissue-specific expression atlas of murine mitochondrial tRNAs |
title_sort | tissue-specific expression atlas of murine mitochondrial trnas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342785/ https://www.ncbi.nlm.nih.gov/pubmed/34265302 http://dx.doi.org/10.1016/j.jbc.2021.100960 |
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