| Literature DB >> 30245104 |
Joanna K Polko1, William J Barnes2, Cătălin Voiniciuc3, Stephanie Doctor1, Blaire Steinwand1, Joseph L Hill4, Ming Tien4, Markus Pauly3, Charles T Anderson2, Joseph J Kieber5.
Abstract
Cell walls play critical roles in plants, regulating tissue mechanics, defining the extent and orientation of cell expansion, and providing a physical barrier against pathogen attack [1]. Cellulose microfibrils, which are synthesized by plasma membrane-localized cellulose synthase (CESA) complexes, are the primary load-bearing elements of plant cell walls [2]. Cell walls are dynamic structures that are regulated in part by cell wall integrity (CWI)-monitoring systems that feed back to modulate wall properties and the synthesis of new wall components [3]. Several receptor-like kinases have been implicated as sensors of CWI [3-5], including the FEI1/FEI2 receptor-like kinases [4]. Here, we characterize two genes encoding novel plant-specific plasma membrane proteins (SHOU4 and SHOU4L) that were identified in a suppressor screen of the cellulose-deficient fei1 fei2 mutant. shou4 shou4l double mutants display phenotypes consistent with elevated levels of cellulose, and elevated levels of non-crystalline cellulose are present in this mutant. Disruption of SHOU4 and SHOU4L increases the abundance of CESA proteins at the plasma membrane as a result of enhanced exocytosis. The SHOU4/4L N-terminal cytosolic domains directly interact with CESAs. Our results suggest that the SHOU4 proteins regulate cellulose synthesis in plants by influencing the trafficking of CESA complexes to the cell surface.Entities:
Keywords: Arabidopsis; cellulose biosynthesis; cellulose synthase; exocytosis; protein trafficking
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Year: 2018 PMID: 30245104 DOI: 10.1016/j.cub.2018.07.076
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834