TY - JOUR
T1 - Making parallel lines meet transferring information from microtubules to extracellular matrix
AU - Baskin, Tobias I.
AU - Gu, Ying
N1 - Funding Information:
Work in the Baskin laboratory on cellulose and the control of growth anisotropy is supported by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the
Funding Information:
US Department of Energy through Grant DE-FG-03ER15421. Work in the Gu laboratory is supported by grants from National Science Foundation (1121375), and The Center for LignoCellulose Structure and Formation, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science under Award Number DE SC0001090.
PY - 2012
Y1 - 2012
N2 - The extracellular matrix is constructed beyond the plasma membrane, challenging mechanisms for its control by the cell. In plants, the cell wall is highly ordered, with cellulose microfibrils aligned coherently over a scale spanning hundreds of cells. To a considerable extent, deploying aligned microfibrils determines mechanical properties of the cell wall, including strength and compliance. Cellulose microfibrils have long been seen to be aligned in parallel with an array of microtubules in the cell cortex. How do these cortical microtu-bules affect the cellulose synthase complex? This question has stood for as many years as the parallelism between the elements has been observed, but now an answer is emerging. Here, we review recent work establishing that the link between microtubules and microfibrils is mediated by a protein named cellulose synthase-interacting protein 1 (CSI1). The protein binds both microtubules and components of the cellulose synthase complex. In the absence of CSI1, micro-fibrils are synthesized but their alignment becomes uncoupled from the microtubules, an effect that is phenocopied in the wild type by depolymerizing the micro-tubules. The characterization of CSI1 significantly enhances knowledge of how cellulose is aligned, a process that serves as a paradigmatic example of how cells dictate the construction of their extracellular environment.
AB - The extracellular matrix is constructed beyond the plasma membrane, challenging mechanisms for its control by the cell. In plants, the cell wall is highly ordered, with cellulose microfibrils aligned coherently over a scale spanning hundreds of cells. To a considerable extent, deploying aligned microfibrils determines mechanical properties of the cell wall, including strength and compliance. Cellulose microfibrils have long been seen to be aligned in parallel with an array of microtubules in the cell cortex. How do these cortical microtu-bules affect the cellulose synthase complex? This question has stood for as many years as the parallelism between the elements has been observed, but now an answer is emerging. Here, we review recent work establishing that the link between microtubules and microfibrils is mediated by a protein named cellulose synthase-interacting protein 1 (CSI1). The protein binds both microtubules and components of the cellulose synthase complex. In the absence of CSI1, micro-fibrils are synthesized but their alignment becomes uncoupled from the microtubules, an effect that is phenocopied in the wild type by depolymerizing the micro-tubules. The characterization of CSI1 significantly enhances knowledge of how cellulose is aligned, a process that serves as a paradigmatic example of how cells dictate the construction of their extracellular environment.
UR - http://www.scopus.com/inward/record.url?scp=84868149349&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84868149349&partnerID=8YFLogxK
U2 - 10.4161/cam.21121
DO - 10.4161/cam.21121
M3 - Article
C2 - 22902763
AN - SCOPUS:84868149349
SN - 1933-6918
VL - 6
SP - 404
EP - 408
JO - Cell Adhesion and Migration
JF - Cell Adhesion and Migration
IS - 5
ER -