Cargando…
Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae
tRNAs in yeast and vertebrate cells move bidirectionally and reversibly between the nucleus and the cytoplasm. We investigated roles of members of the β-importin family in tRNA subcellular dynamics. Retrograde import of tRNA into the nucleus is dependent, directly or indirectly, upon Mtr10. tRNA nuc...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820427/ https://www.ncbi.nlm.nih.gov/pubmed/20032305 http://dx.doi.org/10.1091/mbc.E09-07-0551 |
_version_ | 1782177366083108864 |
---|---|
author | Murthi, Athulaprabha Shaheen, Hussam H. Huang, Hsiao-Yun Preston, Melanie A. Lai, Tsung-Po Phizicky, Eric M. Hopper, Anita K. |
author_facet | Murthi, Athulaprabha Shaheen, Hussam H. Huang, Hsiao-Yun Preston, Melanie A. Lai, Tsung-Po Phizicky, Eric M. Hopper, Anita K. |
author_sort | Murthi, Athulaprabha |
collection | PubMed |
description | tRNAs in yeast and vertebrate cells move bidirectionally and reversibly between the nucleus and the cytoplasm. We investigated roles of members of the β-importin family in tRNA subcellular dynamics. Retrograde import of tRNA into the nucleus is dependent, directly or indirectly, upon Mtr10. tRNA nuclear export utilizes at least two members of the β-importin family. The β-importins involved in nuclear export have shared and exclusive functions. Los1 functions in both the tRNA primary export and the tRNA reexport processes. Msn5 is unable to export tRNAs in the primary round of export if the tRNAs are encoded by intron-containing genes, and for these tRNAs Msn5 functions primarily in their reexport to the cytoplasm. The data support a model in which tRNA retrograde import to the nucleus is a constitutive process; in contrast, reexport of the imported tRNAs back to the cytoplasm is regulated by the availability of nutrients to cells and by tRNA aminoacylation in the nucleus. Finally, we implicate Tef1, the yeast orthologue of translation elongation factor eEF1A, in the tRNA reexport process and show that its subcellular distribution between the nucleus and cytoplasm is dependent upon Mtr10 and Msn5. |
format | Text |
id | pubmed-2820427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-28204272010-04-30 Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae Murthi, Athulaprabha Shaheen, Hussam H. Huang, Hsiao-Yun Preston, Melanie A. Lai, Tsung-Po Phizicky, Eric M. Hopper, Anita K. Mol Biol Cell Articles tRNAs in yeast and vertebrate cells move bidirectionally and reversibly between the nucleus and the cytoplasm. We investigated roles of members of the β-importin family in tRNA subcellular dynamics. Retrograde import of tRNA into the nucleus is dependent, directly or indirectly, upon Mtr10. tRNA nuclear export utilizes at least two members of the β-importin family. The β-importins involved in nuclear export have shared and exclusive functions. Los1 functions in both the tRNA primary export and the tRNA reexport processes. Msn5 is unable to export tRNAs in the primary round of export if the tRNAs are encoded by intron-containing genes, and for these tRNAs Msn5 functions primarily in their reexport to the cytoplasm. The data support a model in which tRNA retrograde import to the nucleus is a constitutive process; in contrast, reexport of the imported tRNAs back to the cytoplasm is regulated by the availability of nutrients to cells and by tRNA aminoacylation in the nucleus. Finally, we implicate Tef1, the yeast orthologue of translation elongation factor eEF1A, in the tRNA reexport process and show that its subcellular distribution between the nucleus and cytoplasm is dependent upon Mtr10 and Msn5. The American Society for Cell Biology 2010-02-15 /pmc/articles/PMC2820427/ /pubmed/20032305 http://dx.doi.org/10.1091/mbc.E09-07-0551 Text en © 2010 by The American Society for Cell Biology |
spellingShingle | Articles Murthi, Athulaprabha Shaheen, Hussam H. Huang, Hsiao-Yun Preston, Melanie A. Lai, Tsung-Po Phizicky, Eric M. Hopper, Anita K. Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title | Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title_full | Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title_fullStr | Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title_full_unstemmed | Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title_short | Regulation of tRNA Bidirectional Nuclear-Cytoplasmic Trafficking in Saccharomyces cerevisiae |
title_sort | regulation of trna bidirectional nuclear-cytoplasmic trafficking in saccharomyces cerevisiae |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820427/ https://www.ncbi.nlm.nih.gov/pubmed/20032305 http://dx.doi.org/10.1091/mbc.E09-07-0551 |
work_keys_str_mv | AT murthiathulaprabha regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT shaheenhussamh regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT huanghsiaoyun regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT prestonmelaniea regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT laitsungpo regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT phizickyericm regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae AT hopperanitak regulationoftrnabidirectionalnuclearcytoplasmictraffickinginsaccharomycescerevisiae |