Cellulose synthase complexes display distinct dynamic behaviors during xylem transdifferentiation
Abstract
In plants, plasma membrane-embedded CELLULOSE SYNTHASE (CESA) enzyme complexes deposit cellulose polymers into the developing cell wall. Cellulose synthesis requires two different sets of CESA complexes that are active during cell expansion and secondary cell wall thickening, respectively. Hence, developing xylem cells, which first undergo cell expansion and subsequently deposit thick secondary walls, need to completely reorganize their CESA complexes from primary wall- to secondary wall-specific CESAs. Using live-cell imaging, we analyzed the principles underlying this remodeling. At the onset of secondary wall synthesis, the primary wall CESAs ceased to be delivered to the plasma membrane and were gradually removed from both the plasma membrane and the Golgi. For a brief transition period, both primary wall- and secondary wall-specific CESAs coexisted in banded domains of the plasma membrane where secondary wall synthesis is concentrated. During this transition, primary and secondary wall CESAs displayed discrete dynamic behaviors and sensitivities to the inhibitor isoxaben. As secondary wall-specific CESAs were delivered and inserted into the plasma membrane, the primary wall CESAs became concentrated in prevacuolar compartments and lytic vacuoles. This adjustment in localization between the two CESAs was accompanied by concurrent decreased primary wall CESA and increased secondary wall CESA protein abundance. Ourmore »
- Authors:
-
- Department of Botany, University of British Columbia, Vancouver, BC V6T 1Z4, Canada,, Department of Wood Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada,
- School of Biosciences, University of Melbourne, Parkville VIC 3010, Australia,, Max Planck Institute for Molecular Plant Physiology, 14476 Potsdam, Germany,
- Department of Wood Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada,
- Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802
- Department of Botany, University of British Columbia, Vancouver, BC V6T 1Z4, Canada,
- School of Biosciences, University of Melbourne, Parkville VIC 3010, Australia,
- Publication Date:
- Research Org.:
- Energy Frontier Research Centers (EFRC), Washington D.C (United States). Center for Lignocellulose Structure and Formation (CLSF)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1440385
- Alternate Identifier(s):
- OSTI ID: 1470632
- Grant/Contract Number:
- SC0001090; RGPIN-2013-229548
- Resource Type:
- Journal Article: Published Article
- Journal Name:
- Proceedings of the National Academy of Sciences of the United States of America
- Additional Journal Information:
- Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Volume: 115 Journal Issue: 27; Journal ID: ISSN 0027-8424
- Publisher:
- Proceedings of the National Academy of Sciences
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES; biofuels (including algae and biomass); bio-inspired; membrane; carbon sequestration; materials and chemistry by design; synthesis (self-assembly); cellulose; primary cell wall; secondary cell wall; cellulose biosynthesis; xylem transdifferentiation
Citation Formats
Watanabe, Yoichiro, Schneider, Rene, Barkwill, Sarah, Gonzales-Vigil, Eliana, Hill, Jr., Joseph L., Samuels, A. Lacey, Persson, Staffan, and Mansfield, Shawn D. Cellulose synthase complexes display distinct dynamic behaviors during xylem transdifferentiation. United States: N. p., 2018.
Web. doi:10.1073/pnas.1802113115.
Watanabe, Yoichiro, Schneider, Rene, Barkwill, Sarah, Gonzales-Vigil, Eliana, Hill, Jr., Joseph L., Samuels, A. Lacey, Persson, Staffan, & Mansfield, Shawn D. Cellulose synthase complexes display distinct dynamic behaviors during xylem transdifferentiation. United States. https://doi.org/10.1073/pnas.1802113115
Watanabe, Yoichiro, Schneider, Rene, Barkwill, Sarah, Gonzales-Vigil, Eliana, Hill, Jr., Joseph L., Samuels, A. Lacey, Persson, Staffan, and Mansfield, Shawn D. 2018.
"Cellulose synthase complexes display distinct dynamic behaviors during xylem transdifferentiation". United States. https://doi.org/10.1073/pnas.1802113115.
@article{osti_1440385,
title = {Cellulose synthase complexes display distinct dynamic behaviors during xylem transdifferentiation},
author = {Watanabe, Yoichiro and Schneider, Rene and Barkwill, Sarah and Gonzales-Vigil, Eliana and Hill, Jr., Joseph L. and Samuels, A. Lacey and Persson, Staffan and Mansfield, Shawn D.},
abstractNote = {In plants, plasma membrane-embedded CELLULOSE SYNTHASE (CESA) enzyme complexes deposit cellulose polymers into the developing cell wall. Cellulose synthesis requires two different sets of CESA complexes that are active during cell expansion and secondary cell wall thickening, respectively. Hence, developing xylem cells, which first undergo cell expansion and subsequently deposit thick secondary walls, need to completely reorganize their CESA complexes from primary wall- to secondary wall-specific CESAs. Using live-cell imaging, we analyzed the principles underlying this remodeling. At the onset of secondary wall synthesis, the primary wall CESAs ceased to be delivered to the plasma membrane and were gradually removed from both the plasma membrane and the Golgi. For a brief transition period, both primary wall- and secondary wall-specific CESAs coexisted in banded domains of the plasma membrane where secondary wall synthesis is concentrated. During this transition, primary and secondary wall CESAs displayed discrete dynamic behaviors and sensitivities to the inhibitor isoxaben. As secondary wall-specific CESAs were delivered and inserted into the plasma membrane, the primary wall CESAs became concentrated in prevacuolar compartments and lytic vacuoles. This adjustment in localization between the two CESAs was accompanied by concurrent decreased primary wall CESA and increased secondary wall CESA protein abundance. Our data reveal distinct and dynamic subcellular trafficking patterns that underpin the remodeling of the cellulose biosynthetic machinery, resulting in the removal and degradation of the primary wall CESA complex with concurrent production and recycling of the secondary wall CESAs.},
doi = {10.1073/pnas.1802113115},
url = {https://www.osti.gov/biblio/1440385},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
issn = {0027-8424},
number = 27,
volume = 115,
place = {United States},
year = {Tue Jun 05 00:00:00 EDT 2018},
month = {Tue Jun 05 00:00:00 EDT 2018}
}
Web of Science
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