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Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome
Influenza A virus RNA genome exists as eight-segmented ribonucleoprotein complexes containing viral RNA polymerase and nucleoprotein (vRNPs). Packaging of vRNPs and virus budding take place at the apical plasma membrane (APM). However, little is known about the molecular mechanisms of apical transpo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120830/ https://www.ncbi.nlm.nih.gov/pubmed/21731653 http://dx.doi.org/10.1371/journal.pone.0021123 |
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author | Momose, Fumitaka Sekimoto, Tetsuya Ohkura, Takashi Jo, Shuichi Kawaguchi, Atsushi Nagata, Kyosuke Morikawa, Yuko |
author_facet | Momose, Fumitaka Sekimoto, Tetsuya Ohkura, Takashi Jo, Shuichi Kawaguchi, Atsushi Nagata, Kyosuke Morikawa, Yuko |
author_sort | Momose, Fumitaka |
collection | PubMed |
description | Influenza A virus RNA genome exists as eight-segmented ribonucleoprotein complexes containing viral RNA polymerase and nucleoprotein (vRNPs). Packaging of vRNPs and virus budding take place at the apical plasma membrane (APM). However, little is known about the molecular mechanisms of apical transport of newly synthesized vRNP. Transfection of fluorescent-labeled antibody and subsequent live cell imaging revealed that punctate vRNP signals moved along microtubules rapidly but intermittently in both directions, suggestive of vesicle trafficking. Using a series of Rab family protein, we demonstrated that progeny vRNP localized to recycling endosome (RE) in an active/GTP-bound Rab11-dependent manner. The vRNP interacted with Rab11 through viral RNA polymerase. The localization of vRNP to RE and subsequent accumulation to the APM were impaired by overexpression of Rab binding domains (RBD) of Rab11 family interacting proteins (Rab11-FIPs). Similarly, no APM accumulation was observed by overexpression of class II Rab11-FIP mutants lacking RBD. These results suggest that the progeny vRNP makes use of Rab11-dependent RE machinery for APM trafficking. |
format | Online Article Text |
id | pubmed-3120830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31208302011-06-30 Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome Momose, Fumitaka Sekimoto, Tetsuya Ohkura, Takashi Jo, Shuichi Kawaguchi, Atsushi Nagata, Kyosuke Morikawa, Yuko PLoS One Research Article Influenza A virus RNA genome exists as eight-segmented ribonucleoprotein complexes containing viral RNA polymerase and nucleoprotein (vRNPs). Packaging of vRNPs and virus budding take place at the apical plasma membrane (APM). However, little is known about the molecular mechanisms of apical transport of newly synthesized vRNP. Transfection of fluorescent-labeled antibody and subsequent live cell imaging revealed that punctate vRNP signals moved along microtubules rapidly but intermittently in both directions, suggestive of vesicle trafficking. Using a series of Rab family protein, we demonstrated that progeny vRNP localized to recycling endosome (RE) in an active/GTP-bound Rab11-dependent manner. The vRNP interacted with Rab11 through viral RNA polymerase. The localization of vRNP to RE and subsequent accumulation to the APM were impaired by overexpression of Rab binding domains (RBD) of Rab11 family interacting proteins (Rab11-FIPs). Similarly, no APM accumulation was observed by overexpression of class II Rab11-FIP mutants lacking RBD. These results suggest that the progeny vRNP makes use of Rab11-dependent RE machinery for APM trafficking. Public Library of Science 2011-06-22 /pmc/articles/PMC3120830/ /pubmed/21731653 http://dx.doi.org/10.1371/journal.pone.0021123 Text en Momose et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Momose, Fumitaka Sekimoto, Tetsuya Ohkura, Takashi Jo, Shuichi Kawaguchi, Atsushi Nagata, Kyosuke Morikawa, Yuko Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title | Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title_full | Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title_fullStr | Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title_full_unstemmed | Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title_short | Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome |
title_sort | apical transport of influenza a virus ribonucleoprotein requires rab11-positive recycling endosome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120830/ https://www.ncbi.nlm.nih.gov/pubmed/21731653 http://dx.doi.org/10.1371/journal.pone.0021123 |
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