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Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors
In yeast, growth and organelle segregation requires formin-dependent assembly of polarized actin cables. These tracks are used by myosin Vs to deliver secretory vesicles for cell growth, organelles for their segregation, and mRNA for fate determination. Several specific receptors have been identifie...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173777/ https://www.ncbi.nlm.nih.gov/pubmed/12642608 http://dx.doi.org/10.1083/jcb.200301035 |
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author | Bretscher, Anthony |
author_facet | Bretscher, Anthony |
author_sort | Bretscher, Anthony |
collection | PubMed |
description | In yeast, growth and organelle segregation requires formin-dependent assembly of polarized actin cables. These tracks are used by myosin Vs to deliver secretory vesicles for cell growth, organelles for their segregation, and mRNA for fate determination. Several specific receptors have been identified that interact with the cargo-binding tails of the myosin Vs. A recent study implicates specific degradation in the bud of the vacuolar receptor, Vac17, as a mechanism for cell cycle–regulated segregation of this organelle. |
format | Text |
id | pubmed-2173777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21737772008-05-01 Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors Bretscher, Anthony J Cell Biol Mini-Review In yeast, growth and organelle segregation requires formin-dependent assembly of polarized actin cables. These tracks are used by myosin Vs to deliver secretory vesicles for cell growth, organelles for their segregation, and mRNA for fate determination. Several specific receptors have been identified that interact with the cargo-binding tails of the myosin Vs. A recent study implicates specific degradation in the bud of the vacuolar receptor, Vac17, as a mechanism for cell cycle–regulated segregation of this organelle. The Rockefeller University Press 2003-03-17 /pmc/articles/PMC2173777/ /pubmed/12642608 http://dx.doi.org/10.1083/jcb.200301035 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Mini-Review Bretscher, Anthony Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title | Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title_full | Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title_fullStr | Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title_full_unstemmed | Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title_short | Polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
title_sort | polarized growth and organelle segregation in yeast: the tracks, motors, and receptors |
topic | Mini-Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173777/ https://www.ncbi.nlm.nih.gov/pubmed/12642608 http://dx.doi.org/10.1083/jcb.200301035 |
work_keys_str_mv | AT bretscheranthony polarizedgrowthandorganellesegregationinyeastthetracksmotorsandreceptors |