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Myosin XI drives polarized growth by vesicle focusing and local enrichment of F-actin inPhyscomitrium patens
Author(s) -
Giulia Galotto,
Pattipong Wisanpitayakorn,
Jeffrey P. Bibeau,
Yen-Chun Liu,
Fabienne Furt,
Ellen Christine Pierce,
Parker J. Simpson,
Erkan Tüzel,
Luis Vidali
Publication year - 2021
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1093/plphys/kiab435
Subject(s) - myosin , actin , vesicle , microbiology and biotechnology , biology , secretory vesicle , tip growth , formins , biophysics , actin cytoskeleton , biochemistry , cell , cytoskeleton , botany , membrane , pollen , pollination , pollen tube
In tip-growing plant cells, growth results from myosin XI and F-actin-mediated deposition of cell wall polysaccharides contained in secretory vesicles. Previous evidence showed that myosin XI anticipates F-actin accumulation at the cell’s tip, suggesting a mechanism where vesicle clustering via myosin XI increases F-actin polymerization. To evaluate this model, we used a conditional loss-of-function strategy by generating moss (Physcomitrium patens) plants harboring a myosin XI temperature-sensitive allele. We found that loss of myosin XI function alters tip cell morphology, vacuolar homeostasis, and cell viability but not following F-actin depolymerization. Importantly, our conditional loss-of-function analysis shows that myosin XI focuses and directs vesicles at the tip of the cell, which induces formin-dependent F-actin polymerization, increasing F-actin’s local concentration. Our findings support the role of myosin XI in vesicle focusing, possibly via clustering and F-actin organization, necessary for tip growth, and deepen our understanding of additional myosin XI functions.

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