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Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles
The tRNA isopentenyltransferases (IPTases), which add an isopentenyl group to N(6) of A37 (i(6)A37) of certain tRNAs, are among a minority of enzymes that modify cytosolic and mitochondrial tRNAs. Pathogenic mutations to the human IPTase, TRIT1, that decrease i(6)A37 levels, cause mitochondrial insu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200024/ https://www.ncbi.nlm.nih.gov/pubmed/32324744 http://dx.doi.org/10.1371/journal.pgen.1008330 |
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author | Khalique, Abdul Mattijssen, Sandy Haddad, Alexander F. Chaudhry, Shereen Maraia, Richard J. |
author_facet | Khalique, Abdul Mattijssen, Sandy Haddad, Alexander F. Chaudhry, Shereen Maraia, Richard J. |
author_sort | Khalique, Abdul |
collection | PubMed |
description | The tRNA isopentenyltransferases (IPTases), which add an isopentenyl group to N(6) of A37 (i(6)A37) of certain tRNAs, are among a minority of enzymes that modify cytosolic and mitochondrial tRNAs. Pathogenic mutations to the human IPTase, TRIT1, that decrease i(6)A37 levels, cause mitochondrial insufficiency that leads to neurodevelopmental disease. We show that TRIT1 encodes an amino-terminal mitochondrial targeting sequence (MTS) that directs mitochondrial import and modification of mitochondrial-tRNAs. Full understanding of IPTase function must consider the tRNAs selected for modification, which vary among species, and in their cytosol and mitochondria. Selection is principally via recognition of the tRNA A36-A37-A38 sequence. An exception is unmodified tRNA(Trp)CCA-A37-A38 in Saccharomyces cerevisiae, whereas tRNA(Trp)CCA is readily modified in Schizosaccharomyces pombe, indicating variable IPTase recognition systems and suggesting that additional exceptions may account for some of the tRNA-i(6)A37 paucity in higher eukaryotes. Yet TRIT1 had not been characterized for restrictive type substrate-specific recognition. We used i(6)A37-dependent tRNA-mediated suppression and i(6)A37-sensitive northern blotting to examine IPTase activities in S. pombe and S. cerevisiae lacking endogenous IPTases on a diversity of tRNA-A36-A37-A38 substrates. Point mutations to the TRIT1 MTS that decrease human mitochondrial import, decrease modification of mitochondrial but not cytosolic tRNAs in both yeasts. TRIT1 exhibits clear substrate-specific restriction against a cytosolic-tRNA(Trp)CCA-A37-A38. Additional data suggest that position 32 of tRNA(Trp)CCA is a conditional determinant for substrate-specific i(6)A37 modification by the restrictive IPTases, Mod5 and TRIT1. The cumulative biochemical and phylogenetic sequence analyses provide new insights into IPTase activities and determinants of tRNA-i(6)A37 profiles in cytosol and mitochondria. |
format | Online Article Text |
id | pubmed-7200024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72000242020-05-12 Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles Khalique, Abdul Mattijssen, Sandy Haddad, Alexander F. Chaudhry, Shereen Maraia, Richard J. PLoS Genet Research Article The tRNA isopentenyltransferases (IPTases), which add an isopentenyl group to N(6) of A37 (i(6)A37) of certain tRNAs, are among a minority of enzymes that modify cytosolic and mitochondrial tRNAs. Pathogenic mutations to the human IPTase, TRIT1, that decrease i(6)A37 levels, cause mitochondrial insufficiency that leads to neurodevelopmental disease. We show that TRIT1 encodes an amino-terminal mitochondrial targeting sequence (MTS) that directs mitochondrial import and modification of mitochondrial-tRNAs. Full understanding of IPTase function must consider the tRNAs selected for modification, which vary among species, and in their cytosol and mitochondria. Selection is principally via recognition of the tRNA A36-A37-A38 sequence. An exception is unmodified tRNA(Trp)CCA-A37-A38 in Saccharomyces cerevisiae, whereas tRNA(Trp)CCA is readily modified in Schizosaccharomyces pombe, indicating variable IPTase recognition systems and suggesting that additional exceptions may account for some of the tRNA-i(6)A37 paucity in higher eukaryotes. Yet TRIT1 had not been characterized for restrictive type substrate-specific recognition. We used i(6)A37-dependent tRNA-mediated suppression and i(6)A37-sensitive northern blotting to examine IPTase activities in S. pombe and S. cerevisiae lacking endogenous IPTases on a diversity of tRNA-A36-A37-A38 substrates. Point mutations to the TRIT1 MTS that decrease human mitochondrial import, decrease modification of mitochondrial but not cytosolic tRNAs in both yeasts. TRIT1 exhibits clear substrate-specific restriction against a cytosolic-tRNA(Trp)CCA-A37-A38. Additional data suggest that position 32 of tRNA(Trp)CCA is a conditional determinant for substrate-specific i(6)A37 modification by the restrictive IPTases, Mod5 and TRIT1. The cumulative biochemical and phylogenetic sequence analyses provide new insights into IPTase activities and determinants of tRNA-i(6)A37 profiles in cytosol and mitochondria. Public Library of Science 2020-04-23 /pmc/articles/PMC7200024/ /pubmed/32324744 http://dx.doi.org/10.1371/journal.pgen.1008330 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Khalique, Abdul Mattijssen, Sandy Haddad, Alexander F. Chaudhry, Shereen Maraia, Richard J. Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title | Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title_full | Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title_fullStr | Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title_full_unstemmed | Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title_short | Targeting mitochondrial and cytosolic substrates of TRIT1 isopentenyltransferase: Specificity determinants and tRNA-i(6)A37 profiles |
title_sort | targeting mitochondrial and cytosolic substrates of trit1 isopentenyltransferase: specificity determinants and trna-i(6)a37 profiles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200024/ https://www.ncbi.nlm.nih.gov/pubmed/32324744 http://dx.doi.org/10.1371/journal.pgen.1008330 |
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