Cargando…
Extensive cargo identification reveals distinct biological roles of the 12 importin pathways
Vast numbers of proteins are transported into and out of the nuclei by approximately 20 species of importin-β family nucleocytoplasmic transport receptors. However, the significance of the multiple parallel transport pathways that the receptors constitute is poorly understood because only limited nu...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305215/ https://www.ncbi.nlm.nih.gov/pubmed/28117667 http://dx.doi.org/10.7554/eLife.21184 |
_version_ | 1782507011453222912 |
---|---|
author | Kimura, Makoto Morinaka, Yuriko Imai, Kenichiro Kose, Shingo Horton, Paul Imamoto, Naoko |
author_facet | Kimura, Makoto Morinaka, Yuriko Imai, Kenichiro Kose, Shingo Horton, Paul Imamoto, Naoko |
author_sort | Kimura, Makoto |
collection | PubMed |
description | Vast numbers of proteins are transported into and out of the nuclei by approximately 20 species of importin-β family nucleocytoplasmic transport receptors. However, the significance of the multiple parallel transport pathways that the receptors constitute is poorly understood because only limited numbers of cargo proteins have been reported. Here, we identified cargo proteins specific to the 12 species of human import receptors with a high-throughput method that employs stable isotope labeling with amino acids in cell culture, an in vitro reconstituted transport system, and quantitative mass spectrometry. The identified cargoes illuminated the manner of cargo allocation to the receptors. The redundancies of the receptors vary widely depending on the cargo protein. Cargoes of the same receptor are functionally related to one another, and the predominant protein groups in the cargo cohorts differ among the receptors. Thus, the receptors are linked to distinct biological processes by the nature of their cargoes. DOI: http://dx.doi.org/10.7554/eLife.21184.001 |
format | Online Article Text |
id | pubmed-5305215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53052152017-02-15 Extensive cargo identification reveals distinct biological roles of the 12 importin pathways Kimura, Makoto Morinaka, Yuriko Imai, Kenichiro Kose, Shingo Horton, Paul Imamoto, Naoko eLife Biochemistry Vast numbers of proteins are transported into and out of the nuclei by approximately 20 species of importin-β family nucleocytoplasmic transport receptors. However, the significance of the multiple parallel transport pathways that the receptors constitute is poorly understood because only limited numbers of cargo proteins have been reported. Here, we identified cargo proteins specific to the 12 species of human import receptors with a high-throughput method that employs stable isotope labeling with amino acids in cell culture, an in vitro reconstituted transport system, and quantitative mass spectrometry. The identified cargoes illuminated the manner of cargo allocation to the receptors. The redundancies of the receptors vary widely depending on the cargo protein. Cargoes of the same receptor are functionally related to one another, and the predominant protein groups in the cargo cohorts differ among the receptors. Thus, the receptors are linked to distinct biological processes by the nature of their cargoes. DOI: http://dx.doi.org/10.7554/eLife.21184.001 eLife Sciences Publications, Ltd 2017-01-24 /pmc/articles/PMC5305215/ /pubmed/28117667 http://dx.doi.org/10.7554/eLife.21184 Text en © 2017, Kimura et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Kimura, Makoto Morinaka, Yuriko Imai, Kenichiro Kose, Shingo Horton, Paul Imamoto, Naoko Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title | Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title_full | Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title_fullStr | Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title_full_unstemmed | Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title_short | Extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
title_sort | extensive cargo identification reveals distinct biological roles of the 12 importin pathways |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305215/ https://www.ncbi.nlm.nih.gov/pubmed/28117667 http://dx.doi.org/10.7554/eLife.21184 |
work_keys_str_mv | AT kimuramakoto extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways AT morinakayuriko extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways AT imaikenichiro extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways AT koseshingo extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways AT hortonpaul extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways AT imamotonaoko extensivecargoidentificationrevealsdistinctbiologicalrolesofthe12importinpathways |