NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i>
The dimension of the plants largest organelle—the vacuole—plays a major role in defining cellular elongation rates. The morphology of the vacuole is controlled by the actin cytoskeleton, but molecular players remain largely unknown. Recently, the Networked (NET) family of membran...
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doaj-e0d01b7a576b4098b3435d60113658b32020-11-25T00:09:54ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-09-012019475210.3390/ijms20194752ijms20194752NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i>Sabrina Kaiser0Ahmed Eisa1Jürgen Kleine-Vehn2David Scheuring3Plant Pathology, University of Kaiserslautern, 67663 Kaiserslautern, GermanyDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Applied Life Sciences (BOKU), 1190 Vienna, AustriaDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Applied Life Sciences (BOKU), 1190 Vienna, AustriaPlant Pathology, University of Kaiserslautern, 67663 Kaiserslautern, GermanyThe dimension of the plants largest organelle—the vacuole—plays a major role in defining cellular elongation rates. The morphology of the vacuole is controlled by the actin cytoskeleton, but molecular players remain largely unknown. Recently, the Networked (NET) family of membrane-associated, actin-binding proteins has been identified. Here, we show that NET4A localizes to highly constricted regions of the vacuolar membrane and contributes to vacuolar morphology. Using genetic interference, we found that deregulation of NET4 abundance increases vacuolar occupancy, and that overexpression of NET4 abundance decreases vacuolar occupancy. Our data reveal that NET4A induces more compact vacuoles, correlating with reduced cellular and organ growth in <i>Arabidopsis thaliana</i>.https://www.mdpi.com/1422-0067/20/19/4752<i>arabidopsis</i>cell biologycell sizeplant growthvacuoleactin cytoskeletonvacuolar occupancycompactness |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sabrina Kaiser Ahmed Eisa Jürgen Kleine-Vehn David Scheuring |
spellingShingle |
Sabrina Kaiser Ahmed Eisa Jürgen Kleine-Vehn David Scheuring NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> International Journal of Molecular Sciences <i>arabidopsis</i> cell biology cell size plant growth vacuole actin cytoskeleton vacuolar occupancy compactness |
author_facet |
Sabrina Kaiser Ahmed Eisa Jürgen Kleine-Vehn David Scheuring |
author_sort |
Sabrina Kaiser |
title |
NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> |
title_short |
NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> |
title_full |
NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> |
title_fullStr |
NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> |
title_full_unstemmed |
NET4 Modulates the Compactness of Vacuoles in <i>Arabidopsis thaliana</i> |
title_sort |
net4 modulates the compactness of vacuoles in <i>arabidopsis thaliana</i> |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2019-09-01 |
description |
The dimension of the plants largest organelle—the vacuole—plays a major role in defining cellular elongation rates. The morphology of the vacuole is controlled by the actin cytoskeleton, but molecular players remain largely unknown. Recently, the Networked (NET) family of membrane-associated, actin-binding proteins has been identified. Here, we show that NET4A localizes to highly constricted regions of the vacuolar membrane and contributes to vacuolar morphology. Using genetic interference, we found that deregulation of NET4 abundance increases vacuolar occupancy, and that overexpression of NET4 abundance decreases vacuolar occupancy. Our data reveal that NET4A induces more compact vacuoles, correlating with reduced cellular and organ growth in <i>Arabidopsis thaliana</i>. |
topic |
<i>arabidopsis</i> cell biology cell size plant growth vacuole actin cytoskeleton vacuolar occupancy compactness |
url |
https://www.mdpi.com/1422-0067/20/19/4752 |
work_keys_str_mv |
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