Key result
Human FHOD1 acts as an actin bundling factor with capping activity toward the filament barbed end, stabilizing actin filaments and mediating F-actin bundling.
No immediate clinical implications; leaves open FHOD1 investigation in cardiac cytoskeletal regulation.
Formins are actin polymerization factors that are known to nucleate and elongate actin filaments at the barbed end. In the present study we show that human FHOD1 lacks actin nucleation and elongation capacity, but acts as an actin bundling factor with capping activity toward the filament barbed end. Constitutively active FHOD1 associates with actin filaments in filopodia and lamellipodia at the leading edge, where it moves with the actin retrograde flow. At the base of lamellipodia, FHOD1 is enriched in nascent, bundled actin arcs as well as in more mature stress fibers. This function requires actin-binding domains located N-terminally to the canonical FH1-FH2 element. The bundling phenotype is maintained in the presence of tropomyosin, confirmed by electron microscopy showing assembly of 5 to 10 actin filaments into parallel, closely spaced filament bundles. Taken together, our data suggest a model in which FHOD1 stabilizes actin filaments by protecting barbed ends from depolymerization with its dimeric FH2 domain, whereas the region N-terminal to the FH1 domain mediates F-actin bundling by simultaneously binding to the sides of adjacent F-actin filaments.
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Schönichen et al. (2013) studied Actin filament dynamics. FHOD1 was evaluated on Actin bundling and capping activity. Human FHOD1 acts as an actin bundling factor with capping activity toward the filament barbed end, stabilizing actin filaments and mediating F-actin bundling.
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