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Abstract Root hairs are single-cell protrusions that enable roots to optimize nutrient and water acquisition. These structures attain their tubular shapes by confining growth to the cell apex, a process called tip growth. The actin cytoskeleton and endomembrane systems are essential for tip growth; however, little is known about how these cellular components coordinate their activities during this process. Here, we show that SPIRRIG (SPI), a beige and Chediak Higashi domain-containing protein involved in membrane trafficking, and BRK1 and SCAR2, subunits of the WAVE/SCAR (W/SC) actin nucleating promoting complex, display polarized localizations in Arabidopsis thaliana root hairs during distinct developmental stages. SPI accumulates at the root hair apex via post-Golgi compartments and positively regulates tip growth by maintaining tip-focused vesicle secretion and filamentous-actin integrity. BRK1 and SCAR2 on the other hand, mark the root hair initiation domain to specify the position of root hair emergence. Consistent with the localization data, tip growth was reduced in spi and the position of root hair emergence was disrupted in brk1 and scar1234. BRK1 depletion coincided with SPI accumulation as root hairs transitioned from initiation to tip growth. Taken together, our work uncovers a role for SPI in facilitating actin-dependent root hair development in Arabidopsis through pathways that might intersect with W/SC.
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Tip Growth
Pollen tubes and root hairs grow by a highly focused deposition of new wall and membrane materials at their growing apex. Comparison of the machinery that localises such growth between these cell types has revealed common components, providing important insight into how plant cells control cell expansion. Such elements include the small GTPases (e.g. ROPs and RABs), gradients and intricate spatial patterning in the fluxes of ions (e.g. Ca2+ and H+) and partitioning of membrane lipids (such as the phosphoinositides). These regulators are coupled to focused action of the secretory machinery (e.g. the exocyst) and cytoskeletal dynamics, with integral roles emerging for actin, tubulin and their associated motor proteins. These components form an integrated regulatory network that imposes robust spatial localisation of the growth machinery and so supports the production of an elongating tube-like growth form where cell expansion is limited to the very apex, that is, tip growth.
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- PAR ID:
- 10045464
- Date Published:
- Journal Name:
- Encyclopedia of life sciences
- ISSN:
- 1476-9506
- Page Range / eLocation ID:
- 1-8
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1002/9780470015902.a0023746
