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Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes
The Saccharomyces cerevisiae myosin-V, Myo2p, is essential for polarized growth, most likely through transport of secretory vesicles to the developing bud. Myo2p is also required for vacuole movement, a process not essential for growth. The globular region of the myosin-V COOH-terminal tail domain i...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175197/ https://www.ncbi.nlm.nih.gov/pubmed/10931864 |
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author | Catlett, Natalie L. Duex, Jason E. Tang, Fusheng Weisman, Lois S. |
author_facet | Catlett, Natalie L. Duex, Jason E. Tang, Fusheng Weisman, Lois S. |
author_sort | Catlett, Natalie L. |
collection | PubMed |
description | The Saccharomyces cerevisiae myosin-V, Myo2p, is essential for polarized growth, most likely through transport of secretory vesicles to the developing bud. Myo2p is also required for vacuole movement, a process not essential for growth. The globular region of the myosin-V COOH-terminal tail domain is proposed to bind cargo. Through random mutagenesis of this globular tail, we isolated six new single point mutants defective in vacuole inheritance, but not polarized growth. These point mutations cluster to four amino acids in an 11-amino acid span, suggesting that this region is important for vacuole movement. In addition, through characterization of myo2-ΔAflII, a deletion of amino acids 1,459–1,491, we identified a second region of the globular tail specifically required for polarized growth. Whereas this mutant does not support growth, it complements the vacuole inheritance defect in myo2-2 (G1248D) cells. Moreover, overexpression of the myo2-ΔAflII globular tail interferes with vacuole movement, but not polarized growth. These data indicate that this second region is dispensable for vacuole movement. The identification of these distinct subdomains in the cargo-binding domain suggests how myosin-Vs can move multiple cargoes. Moreover, these studies suggest that the vacuole receptor for Myo2p differs from the receptor for the essential cargo. |
format | Text |
id | pubmed-2175197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21751972008-05-01 Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes Catlett, Natalie L. Duex, Jason E. Tang, Fusheng Weisman, Lois S. J Cell Biol Original Article The Saccharomyces cerevisiae myosin-V, Myo2p, is essential for polarized growth, most likely through transport of secretory vesicles to the developing bud. Myo2p is also required for vacuole movement, a process not essential for growth. The globular region of the myosin-V COOH-terminal tail domain is proposed to bind cargo. Through random mutagenesis of this globular tail, we isolated six new single point mutants defective in vacuole inheritance, but not polarized growth. These point mutations cluster to four amino acids in an 11-amino acid span, suggesting that this region is important for vacuole movement. In addition, through characterization of myo2-ΔAflII, a deletion of amino acids 1,459–1,491, we identified a second region of the globular tail specifically required for polarized growth. Whereas this mutant does not support growth, it complements the vacuole inheritance defect in myo2-2 (G1248D) cells. Moreover, overexpression of the myo2-ΔAflII globular tail interferes with vacuole movement, but not polarized growth. These data indicate that this second region is dispensable for vacuole movement. The identification of these distinct subdomains in the cargo-binding domain suggests how myosin-Vs can move multiple cargoes. Moreover, these studies suggest that the vacuole receptor for Myo2p differs from the receptor for the essential cargo. The Rockefeller University Press 2000-08-07 /pmc/articles/PMC2175197/ /pubmed/10931864 Text en © 2000 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 | Original Article Catlett, Natalie L. Duex, Jason E. Tang, Fusheng Weisman, Lois S. Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title | Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title_full | Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title_fullStr | Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title_full_unstemmed | Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title_short | Two Distinct Regions in a Yeast Myosin-V Tail Domain Are Required for the Movement of Different Cargoes |
title_sort | two distinct regions in a yeast myosin-v tail domain are required for the movement of different cargoes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175197/ https://www.ncbi.nlm.nih.gov/pubmed/10931864 |
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