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Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease
Protein prenylation is a widespread post-translational modification in eukaryotes that plays a crucial role in membrane targeting and signal transduction. RabGTPases is the largest group of post-translationally C-terminally geranylgeranylated. All Rabs are processed by Rab geranylgeranyl-transferase...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864799/ https://www.ncbi.nlm.nih.gov/pubmed/24358126 http://dx.doi.org/10.1371/journal.pone.0081758 |
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author | Köhnke, Monika Delon, Christine Hastie, Marcus L. Nguyen, Uyen T. T. Wu, Yao-Wen Waldmann, Herbert Goody, Roger S. Gorman, Jeffrey J. Alexandrov, Kirill |
author_facet | Köhnke, Monika Delon, Christine Hastie, Marcus L. Nguyen, Uyen T. T. Wu, Yao-Wen Waldmann, Herbert Goody, Roger S. Gorman, Jeffrey J. Alexandrov, Kirill |
author_sort | Köhnke, Monika |
collection | PubMed |
description | Protein prenylation is a widespread post-translational modification in eukaryotes that plays a crucial role in membrane targeting and signal transduction. RabGTPases is the largest group of post-translationally C-terminally geranylgeranylated. All Rabs are processed by Rab geranylgeranyl-transferase and Rab escort protein (REP). Human genetic defects resulting in the loss one of two REP isoforms REP-1, lead to underprenylation of RabGTPases that manifests in retinal degradation and blindness known as choroideremia. In this study we used a combination of microinjections and chemo-enzymatic tagging to establish whether Rab GTPases are prenylated and delivered to their target cellular membranes with the same rate. We demonstrate that although all tested Rab GTPases display the same rate of membrane delivery, the extent of Rab prenylation in 5 hour time window vary by more than an order of magnitude. We found that Rab27a, Rab27b, Rab38 and Rab42 display the slowest prenylation in vivo and in the cell. Our work points to possible contribution of Rab38 to the emergence of choroideremia in addition to Rab27a and Rab27b. |
format | Online Article Text |
id | pubmed-3864799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38647992013-12-19 Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease Köhnke, Monika Delon, Christine Hastie, Marcus L. Nguyen, Uyen T. T. Wu, Yao-Wen Waldmann, Herbert Goody, Roger S. Gorman, Jeffrey J. Alexandrov, Kirill PLoS One Research Article Protein prenylation is a widespread post-translational modification in eukaryotes that plays a crucial role in membrane targeting and signal transduction. RabGTPases is the largest group of post-translationally C-terminally geranylgeranylated. All Rabs are processed by Rab geranylgeranyl-transferase and Rab escort protein (REP). Human genetic defects resulting in the loss one of two REP isoforms REP-1, lead to underprenylation of RabGTPases that manifests in retinal degradation and blindness known as choroideremia. In this study we used a combination of microinjections and chemo-enzymatic tagging to establish whether Rab GTPases are prenylated and delivered to their target cellular membranes with the same rate. We demonstrate that although all tested Rab GTPases display the same rate of membrane delivery, the extent of Rab prenylation in 5 hour time window vary by more than an order of magnitude. We found that Rab27a, Rab27b, Rab38 and Rab42 display the slowest prenylation in vivo and in the cell. Our work points to possible contribution of Rab38 to the emergence of choroideremia in addition to Rab27a and Rab27b. Public Library of Science 2013-12-16 /pmc/articles/PMC3864799/ /pubmed/24358126 http://dx.doi.org/10.1371/journal.pone.0081758 Text en © 2013 Köhnke 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 Köhnke, Monika Delon, Christine Hastie, Marcus L. Nguyen, Uyen T. T. Wu, Yao-Wen Waldmann, Herbert Goody, Roger S. Gorman, Jeffrey J. Alexandrov, Kirill Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title | Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title_full | Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title_fullStr | Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title_full_unstemmed | Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title_short | Rab GTPase Prenylation Hierarchy and Its Potential Role in Choroideremia Disease |
title_sort | rab gtpase prenylation hierarchy and its potential role in choroideremia disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864799/ https://www.ncbi.nlm.nih.gov/pubmed/24358126 http://dx.doi.org/10.1371/journal.pone.0081758 |
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