Kar9 symmetry breaking alone is insufficient to ensure spindle alignment

Abstract Spindle positioning must be tightly regulated to ensure asymmetric cell divisions are successful. In budding yeast, spindle positioning is mediated by the asymmetric localization of microtubule + end tracking protein Kar9. Kar9 asymmetry is believed to be essential for spindle alignment. Ho...

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Autores principales: Miram Meziane, Rachel Genthial, Jackie Vogel
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/fa04e7d4d13a495c8b0ef53736aaf624
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spelling oai:doaj.org-article:fa04e7d4d13a495c8b0ef53736aaf6242021-12-02T12:11:52ZKar9 symmetry breaking alone is insufficient to ensure spindle alignment10.1038/s41598-021-83136-w2045-2322https://doaj.org/article/fa04e7d4d13a495c8b0ef53736aaf6242021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-83136-whttps://doaj.org/toc/2045-2322Abstract Spindle positioning must be tightly regulated to ensure asymmetric cell divisions are successful. In budding yeast, spindle positioning is mediated by the asymmetric localization of microtubule + end tracking protein Kar9. Kar9 asymmetry is believed to be essential for spindle alignment. However, the temporal correlation between symmetry breaking and spindle alignment has not been measured. Here, we establish a method of quantifying Kar9 symmetry breaking and find that Kar9 asymmetry is not well coupled with stable spindle alignment. We report the spindles are not aligned in the majority of asymmetric cells. Rather, stable alignment is correlated with Kar9 residence in the bud, regardless of symmetry state. Our findings suggest that Kar9 asymmetry alone is insufficient for stable alignment and reveal a possible role for Swe1 in regulating Kar9 residence in the bud.Miram MezianeRachel GenthialJackie VogelNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Miram Meziane
Rachel Genthial
Jackie Vogel
Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
description Abstract Spindle positioning must be tightly regulated to ensure asymmetric cell divisions are successful. In budding yeast, spindle positioning is mediated by the asymmetric localization of microtubule + end tracking protein Kar9. Kar9 asymmetry is believed to be essential for spindle alignment. However, the temporal correlation between symmetry breaking and spindle alignment has not been measured. Here, we establish a method of quantifying Kar9 symmetry breaking and find that Kar9 asymmetry is not well coupled with stable spindle alignment. We report the spindles are not aligned in the majority of asymmetric cells. Rather, stable alignment is correlated with Kar9 residence in the bud, regardless of symmetry state. Our findings suggest that Kar9 asymmetry alone is insufficient for stable alignment and reveal a possible role for Swe1 in regulating Kar9 residence in the bud.
format article
author Miram Meziane
Rachel Genthial
Jackie Vogel
author_facet Miram Meziane
Rachel Genthial
Jackie Vogel
author_sort Miram Meziane
title Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
title_short Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
title_full Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
title_fullStr Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
title_full_unstemmed Kar9 symmetry breaking alone is insufficient to ensure spindle alignment
title_sort kar9 symmetry breaking alone is insufficient to ensure spindle alignment
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/fa04e7d4d13a495c8b0ef53736aaf624
work_keys_str_mv AT mirammeziane kar9symmetrybreakingaloneisinsufficienttoensurespindlealignment
AT rachelgenthial kar9symmetrybreakingaloneisinsufficienttoensurespindlealignment
AT jackievogel kar9symmetrybreakingaloneisinsufficienttoensurespindlealignment
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