Immuno-reactant to RhoA antibody co-localizes with cortical actin filaments in guard cells of open stomata inCommelina communis L.

Abstract

Stomatal regulation is essential for the growth of land plants. Pairs of guard cells that delineate the stomata perceive stimuli and respond to acquire the optimum aperture. The actin cytoskeleton participates in signaling pathways of the guard cell (Kim et al., 1995; Eun and Lee, 1997; Hwang et al., 1997). To identify the upstream molecules that regulate actin dynamics in plant cells, we immunoblotted proteins extracted from leaves ofCommelina commuais L. with the RhoA antibody, and identified one band of 26KD from the epidermis. Using immunofluorescence microscopy, we examined the subcellular distribution of the immuno-reactant(s) in guard cells. When stomata were open under light, the organization of the immuno-reactant(s) resembled the radial arrangement of cortical actin filaments of guard cells. Double-labeling of the guard cells, using the RhoA and actin antibodies as primary antibodies, showed that the immuno-reactant(s) of the RhoA antibody and actin filaments co-localized in the cortex of illuminated guard cells. However, the pattern was not found in guard cells when stomata were closed under darkness or by ABA, conditions under which cortical actin proteins are disassembled in guard cells. From these observations, we can suggest the possible presence of a RhoA-like protein and its involvement in the organization of the actin cytoskeleton in guard cells.