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Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family

The Arabidopsis thaliana genome encodes 13 myosin XI motor proteins. Previous insertional mutant analysis has implicated substantial redundancy of function of plant myosin XIs in transport of intracellular organelles. Considerable information is available about the interaction of cargo with the myos...

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Autores principales: Sattarzadeh, Amirali, Schmelzer, Elmon, Hanson, Maureen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355782/
https://www.ncbi.nlm.nih.gov/pubmed/22645548
http://dx.doi.org/10.3389/fpls.2011.00072
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author Sattarzadeh, Amirali
Schmelzer, Elmon
Hanson, Maureen R.
author_facet Sattarzadeh, Amirali
Schmelzer, Elmon
Hanson, Maureen R.
author_sort Sattarzadeh, Amirali
collection PubMed
description The Arabidopsis thaliana genome encodes 13 myosin XI motor proteins. Previous insertional mutant analysis has implicated substantial redundancy of function of plant myosin XIs in transport of intracellular organelles. Considerable information is available about the interaction of cargo with the myosin XI-homologous yeast myosin V protein myo2p. We identified a region in each of 12 myosin XI sequences that correspond to the yeast myo2p secretory-vesicle binding domain (the “DIL” domain). Structural modeling of the myosin DIL domain region of plant myosin XIs revealed significant similarity to the yeast myo2p and myo4p DIL domains. Transient expression of YFP fusions with the Arabidopsis myosin XI DIL domain resulted in fluorescent labeling of a variety of organelles, including the endoplasmic reticulum, peroxisomes, Golgi, and nuclear envelope. With the exception of the YFP::MYA1 DIL fusion, expression of the DIL–YFP fusions resulted in loss of motility of labeled organelles, consistent with a dominant-negative effect. Certain fusions resulted in localization to the cytoplasm, plasma membrane, or to unidentified vesicles. The same YFP-domain fusion sometimes labeled more than one organelle. Expression of a YFP fusion to a yeast myo2p DIL domain resulted in labeling of plant peroxisomes. Fusions with some of the myosin XI domains resulted in labeling of known cargoes of the particular myosin XI; however, certain myosin XI YFP fusions labeled organelles that had not previously been found to be detectably affected by mutations nor by expression of dominant-negative constructs.
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spelling pubmed-33557822012-05-29 Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family Sattarzadeh, Amirali Schmelzer, Elmon Hanson, Maureen R. Front Plant Sci Plant Science The Arabidopsis thaliana genome encodes 13 myosin XI motor proteins. Previous insertional mutant analysis has implicated substantial redundancy of function of plant myosin XIs in transport of intracellular organelles. Considerable information is available about the interaction of cargo with the myosin XI-homologous yeast myosin V protein myo2p. We identified a region in each of 12 myosin XI sequences that correspond to the yeast myo2p secretory-vesicle binding domain (the “DIL” domain). Structural modeling of the myosin DIL domain region of plant myosin XIs revealed significant similarity to the yeast myo2p and myo4p DIL domains. Transient expression of YFP fusions with the Arabidopsis myosin XI DIL domain resulted in fluorescent labeling of a variety of organelles, including the endoplasmic reticulum, peroxisomes, Golgi, and nuclear envelope. With the exception of the YFP::MYA1 DIL fusion, expression of the DIL–YFP fusions resulted in loss of motility of labeled organelles, consistent with a dominant-negative effect. Certain fusions resulted in localization to the cytoplasm, plasma membrane, or to unidentified vesicles. The same YFP-domain fusion sometimes labeled more than one organelle. Expression of a YFP fusion to a yeast myo2p DIL domain resulted in labeling of plant peroxisomes. Fusions with some of the myosin XI domains resulted in labeling of known cargoes of the particular myosin XI; however, certain myosin XI YFP fusions labeled organelles that had not previously been found to be detectably affected by mutations nor by expression of dominant-negative constructs. Frontiers Research Foundation 2011-11-03 /pmc/articles/PMC3355782/ /pubmed/22645548 http://dx.doi.org/10.3389/fpls.2011.00072 Text en Copyright © 2011 Sattarzadeh, Schmelzer and Hanson. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Plant Science
Sattarzadeh, Amirali
Schmelzer, Elmon
Hanson, Maureen R.
Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title_full Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title_fullStr Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title_full_unstemmed Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title_short Analysis of Organelle Targeting by DIL Domains of the Arabidopsis Myosin XI Family
title_sort analysis of organelle targeting by dil domains of the arabidopsis myosin xi family
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355782/
https://www.ncbi.nlm.nih.gov/pubmed/22645548
http://dx.doi.org/10.3389/fpls.2011.00072
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