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Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision
tRNAs that are transcribed in the nucleus are exported to the cytoplasm to perform their iterative essential function in translation. However, the complex set of tRNA post-transcriptional processing and subcellular trafficking steps are not completely understood. In particular, proteins involved in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508810/ https://www.ncbi.nlm.nih.gov/pubmed/36099418 http://dx.doi.org/10.1093/nar/gkac754 |
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author | Chatterjee, Kunal Marshall, William A Hopper, Anita K |
author_facet | Chatterjee, Kunal Marshall, William A Hopper, Anita K |
author_sort | Chatterjee, Kunal |
collection | PubMed |
description | tRNAs that are transcribed in the nucleus are exported to the cytoplasm to perform their iterative essential function in translation. However, the complex set of tRNA post-transcriptional processing and subcellular trafficking steps are not completely understood. In particular, proteins involved in tRNA nuclear export remain unknown since the canonical tRNA nuclear exportin, Los1/Exportin-t, is unessential in all tested organisms. We previously reported that budding yeast Mex67-Mtr2, a mRNA nuclear exporter, co-functions with Los1 in tRNA nuclear export. Here we employed in vivo co-purification of tRNAs with endogenously expressed nuclear exporters to document that Crm1 also is a bona fide tRNA nuclear exporter. We document that Los1, Mex67-Mtr2 and Crm1 possess individual tRNA preferences for forming nuclear export complexes with members of the 10 families of intron-containing pre-tRNAs. Remarkably, Mex67-Mtr2, but not Los1 or Crm1, is error-prone, delivering tRNAs to the cytoplasm prior to 5′ leader removal. tRNA retrograde nuclear import functions to monitor the aberrant leader-containing spliced tRNAs, returning them to the nucleus where they are degraded by 3′ to 5′ exonucleases. Overall, our work identifies a new tRNA nuclear exporter, uncovers exporter preferences for specific tRNA families, and documents contribution of tRNA nuclear import to tRNA quality control. |
format | Online Article Text |
id | pubmed-9508810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95088102022-09-26 Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision Chatterjee, Kunal Marshall, William A Hopper, Anita K Nucleic Acids Res RNA and RNA-protein complexes tRNAs that are transcribed in the nucleus are exported to the cytoplasm to perform their iterative essential function in translation. However, the complex set of tRNA post-transcriptional processing and subcellular trafficking steps are not completely understood. In particular, proteins involved in tRNA nuclear export remain unknown since the canonical tRNA nuclear exportin, Los1/Exportin-t, is unessential in all tested organisms. We previously reported that budding yeast Mex67-Mtr2, a mRNA nuclear exporter, co-functions with Los1 in tRNA nuclear export. Here we employed in vivo co-purification of tRNAs with endogenously expressed nuclear exporters to document that Crm1 also is a bona fide tRNA nuclear exporter. We document that Los1, Mex67-Mtr2 and Crm1 possess individual tRNA preferences for forming nuclear export complexes with members of the 10 families of intron-containing pre-tRNAs. Remarkably, Mex67-Mtr2, but not Los1 or Crm1, is error-prone, delivering tRNAs to the cytoplasm prior to 5′ leader removal. tRNA retrograde nuclear import functions to monitor the aberrant leader-containing spliced tRNAs, returning them to the nucleus where they are degraded by 3′ to 5′ exonucleases. Overall, our work identifies a new tRNA nuclear exporter, uncovers exporter preferences for specific tRNA families, and documents contribution of tRNA nuclear import to tRNA quality control. Oxford University Press 2022-09-13 /pmc/articles/PMC9508810/ /pubmed/36099418 http://dx.doi.org/10.1093/nar/gkac754 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA and RNA-protein complexes Chatterjee, Kunal Marshall, William A Hopper, Anita K Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title | Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title_full | Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title_fullStr | Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title_full_unstemmed | Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title_short | Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision |
title_sort | three trna nuclear exporters in s. cerevisiae: parallel pathways, preferences, and precision |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508810/ https://www.ncbi.nlm.nih.gov/pubmed/36099418 http://dx.doi.org/10.1093/nar/gkac754 |
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