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Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site

Bipolar spindle formation in yeast requires insertion of centrosomes (known as spindle pole bodies [SPBs]) into fenestrated regions of the nuclear envelope (NE). Using structured illumination microscopy and bimolecular fluorescence complementation, we map protein distribution at SPB fenestrae and in...

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Autores principales: Chen, Jingjing, Gardner, Jennifer M., Yu, Zulin, Smith, Sarah E., McKinney, Sean, Slaughter, Brian D., Unruh, Jay R., Jaspersen, Sue L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504903/
https://www.ncbi.nlm.nih.gov/pubmed/30862629
http://dx.doi.org/10.1083/jcb.201809045
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author Chen, Jingjing
Gardner, Jennifer M.
Yu, Zulin
Smith, Sarah E.
McKinney, Sean
Slaughter, Brian D.
Unruh, Jay R.
Jaspersen, Sue L.
author_facet Chen, Jingjing
Gardner, Jennifer M.
Yu, Zulin
Smith, Sarah E.
McKinney, Sean
Slaughter, Brian D.
Unruh, Jay R.
Jaspersen, Sue L.
author_sort Chen, Jingjing
collection PubMed
description Bipolar spindle formation in yeast requires insertion of centrosomes (known as spindle pole bodies [SPBs]) into fenestrated regions of the nuclear envelope (NE). Using structured illumination microscopy and bimolecular fluorescence complementation, we map protein distribution at SPB fenestrae and interrogate protein–protein interactions with high spatial resolution. We find that the Sad1-UNC-84 (SUN) protein Mps3 forms a ring-like structure around the SPB, similar to toroids seen for components of the SPB insertion network (SPIN). Mps3 and the SPIN component Mps2 (a Klarsicht-ANC-1-Syne-1 domain [KASH]–like protein) form a novel noncanonical linker of nucleoskeleton and cytoskeleton (LINC) complex that is connected in both luminal and extraluminal domains at the site of SPB insertion. The LINC complex also controls the distribution of a soluble SPIN component Bbp1. Taken together, our work shows that Mps3 is a fifth SPIN component and suggests both direct and indirect roles for the LINC complex in NE remodeling.
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spelling pubmed-65049032019-05-21 Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site Chen, Jingjing Gardner, Jennifer M. Yu, Zulin Smith, Sarah E. McKinney, Sean Slaughter, Brian D. Unruh, Jay R. Jaspersen, Sue L. J Cell Biol Research Articles Bipolar spindle formation in yeast requires insertion of centrosomes (known as spindle pole bodies [SPBs]) into fenestrated regions of the nuclear envelope (NE). Using structured illumination microscopy and bimolecular fluorescence complementation, we map protein distribution at SPB fenestrae and interrogate protein–protein interactions with high spatial resolution. We find that the Sad1-UNC-84 (SUN) protein Mps3 forms a ring-like structure around the SPB, similar to toroids seen for components of the SPB insertion network (SPIN). Mps3 and the SPIN component Mps2 (a Klarsicht-ANC-1-Syne-1 domain [KASH]–like protein) form a novel noncanonical linker of nucleoskeleton and cytoskeleton (LINC) complex that is connected in both luminal and extraluminal domains at the site of SPB insertion. The LINC complex also controls the distribution of a soluble SPIN component Bbp1. Taken together, our work shows that Mps3 is a fifth SPIN component and suggests both direct and indirect roles for the LINC complex in NE remodeling. Rockefeller University Press 2019-05-06 2019-03-12 /pmc/articles/PMC6504903/ /pubmed/30862629 http://dx.doi.org/10.1083/jcb.201809045 Text en © 2019 Chen et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Chen, Jingjing
Gardner, Jennifer M.
Yu, Zulin
Smith, Sarah E.
McKinney, Sean
Slaughter, Brian D.
Unruh, Jay R.
Jaspersen, Sue L.
Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title_full Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title_fullStr Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title_full_unstemmed Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title_short Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
title_sort yeast centrosome components form a noncanonical linc complex at the nuclear envelope insertion site
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504903/
https://www.ncbi.nlm.nih.gov/pubmed/30862629
http://dx.doi.org/10.1083/jcb.201809045
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