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Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization

Multisubunit members of the CATCHR family: COG and NRZ complexes, mediate intra-Golgi and Golgi to ER vesicle tethering, respectively. We systematically addressed the genetic and functional interrelationships between Rabs, Kifs, and the retrograde CATCHR family proteins: COG3 and ZW10, which are nec...

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Autores principales: Liu, Shijie, Majeed, Waqar, Grigaitis, Pranas, Betts, Matthew J., Climer, Leslie K., Starkuviene, Vytaute, Storrie, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687757/
https://www.ncbi.nlm.nih.gov/pubmed/31428608
http://dx.doi.org/10.3389/fcell.2019.00126
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author Liu, Shijie
Majeed, Waqar
Grigaitis, Pranas
Betts, Matthew J.
Climer, Leslie K.
Starkuviene, Vytaute
Storrie, Brian
author_facet Liu, Shijie
Majeed, Waqar
Grigaitis, Pranas
Betts, Matthew J.
Climer, Leslie K.
Starkuviene, Vytaute
Storrie, Brian
author_sort Liu, Shijie
collection PubMed
description Multisubunit members of the CATCHR family: COG and NRZ complexes, mediate intra-Golgi and Golgi to ER vesicle tethering, respectively. We systematically addressed the genetic and functional interrelationships between Rabs, Kifs, and the retrograde CATCHR family proteins: COG3 and ZW10, which are necessary to maintain the organization of the Golgi complex. We scored the ability of siRNAs targeting 19 Golgi-associated Rab proteins and all 44 human Kifs, microtubule-dependent motor proteins, to suppress CATCHR-dependent Golgi fragmentation in an epistatic fluorescent microscopy-based assay. We found that co-depletion of Rab6A, Rab6A’, Rab27A, Rab39A and two minus-end Kifs, namely KIFC3 and KIF25, suppressed both COG3- and ZW10-depletion-induced Golgi fragmentation. ZW10-dependent Golgi fragmentation was suppressed selectively by a separate set of Rabs: Rab11A, Rab33B and the little characterized Rab29. 10 Kifs were identified as hits in ZW10-depletion-induced Golgi fragmentation, and, in contrast to the double suppressive Kifs, these were predominantly plus-end motors. No Rabs or Kifs selectively suppressed COG3-depletion-induced Golgi fragmentation. Protein-protein interaction network analysis indicated putative direct and indirect links between suppressive Rabs and tether function. Validation of the suppressive hits by EM confirmed a restored organization of the Golgi cisternal stack. Based on these outcomes, we propose a three-way competitive model of Golgi organization in which Rabs, Kifs and tethers modulate sequentially the balance between Golgi-derived vesicle formation, consumption, and off-Golgi transport.
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spelling pubmed-66877572019-08-19 Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization Liu, Shijie Majeed, Waqar Grigaitis, Pranas Betts, Matthew J. Climer, Leslie K. Starkuviene, Vytaute Storrie, Brian Front Cell Dev Biol Cell and Developmental Biology Multisubunit members of the CATCHR family: COG and NRZ complexes, mediate intra-Golgi and Golgi to ER vesicle tethering, respectively. We systematically addressed the genetic and functional interrelationships between Rabs, Kifs, and the retrograde CATCHR family proteins: COG3 and ZW10, which are necessary to maintain the organization of the Golgi complex. We scored the ability of siRNAs targeting 19 Golgi-associated Rab proteins and all 44 human Kifs, microtubule-dependent motor proteins, to suppress CATCHR-dependent Golgi fragmentation in an epistatic fluorescent microscopy-based assay. We found that co-depletion of Rab6A, Rab6A’, Rab27A, Rab39A and two minus-end Kifs, namely KIFC3 and KIF25, suppressed both COG3- and ZW10-depletion-induced Golgi fragmentation. ZW10-dependent Golgi fragmentation was suppressed selectively by a separate set of Rabs: Rab11A, Rab33B and the little characterized Rab29. 10 Kifs were identified as hits in ZW10-depletion-induced Golgi fragmentation, and, in contrast to the double suppressive Kifs, these were predominantly plus-end motors. No Rabs or Kifs selectively suppressed COG3-depletion-induced Golgi fragmentation. Protein-protein interaction network analysis indicated putative direct and indirect links between suppressive Rabs and tether function. Validation of the suppressive hits by EM confirmed a restored organization of the Golgi cisternal stack. Based on these outcomes, we propose a three-way competitive model of Golgi organization in which Rabs, Kifs and tethers modulate sequentially the balance between Golgi-derived vesicle formation, consumption, and off-Golgi transport. Frontiers Media S.A. 2019-08-02 /pmc/articles/PMC6687757/ /pubmed/31428608 http://dx.doi.org/10.3389/fcell.2019.00126 Text en Copyright © 2019 Liu, Majeed, Grigaitis, Betts, Climer, Starkuviene and Storrie. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Liu, Shijie
Majeed, Waqar
Grigaitis, Pranas
Betts, Matthew J.
Climer, Leslie K.
Starkuviene, Vytaute
Storrie, Brian
Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title_full Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title_fullStr Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title_full_unstemmed Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title_short Epistatic Analysis of the Contribution of Rabs and Kifs to CATCHR Family Dependent Golgi Organization
title_sort epistatic analysis of the contribution of rabs and kifs to catchr family dependent golgi organization
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687757/
https://www.ncbi.nlm.nih.gov/pubmed/31428608
http://dx.doi.org/10.3389/fcell.2019.00126
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