Supra-organismal regulation of strigolactone exudation and plant development in response to rhizospheric cues in rice.

Plants have evolved elaborate mechanisms to detect neighboring plants, which typically involve the perception of "cues" inadvertently produced by the neighbor. 1 Strigolactones are hormonal signaling molecules 2,3 that are also exuded into the rhizosphere by most flowering plant species to promote arbuscular mycorrhizal symbioses. 4 Since flowering plants have an endogenous perception system for strigolactones, 5 strigolactones are obvious candidates to act as a cue for neighbor presence, but have not been shown to act as such. To test this hypothesis in rice plants, we quantified two major strigolactones of rice plants, orobanchol and 4-deoxyorobanchol, in root exudates by using LC-MS/MS (MRM) and examined feedback regulation of strigolactone biosynthesis and changes in shoot branching phenotypes in rice plants grown at different densities in hydroponics and soil culture. We show that the presence of neighboring plants, or greater root volume, results in rapidly induced changes in strigolactone biosynthesis, sensitivity, and exudation and the subsequent longer-term changes in shoot architecture. These changes require intact strigolactone biosynthesis in neighboring plants and intact strigolactone signaling in focal plants. These results suggest that strigolactone biosynthesis and exudation in rice plants are driven by supra-organismal environmental strigolactone levels. Strigolactones thus act as a cue for neighbor presence in rice plants, but also seem to act as a more general root density-sensing mechanism in flowering plants that integrates soil volume and neighbor density and allows plants to adapt to the limitations of the rhizosphere. • Crowding reduces biosynthesis and exudation of strigolactones • This density-dependent response requires strigolactone perception • Strigolactone biosynthesis and exudation respond to environmental strigolactones • Crowding in soil reduces strigolactone exudation and shoot branching in rice plants Strigolactones (SLs) trigger parasitism and symbiosis in the rhizosphere and function as a hormone in plants. Yoneyama et al. demonstrate that rice plants sense SLs in the rhizosphere and regulate their SL biosynthesis and exudation, suggesting that SLs act as a cue for a plant-plant communication in rice plants. [ABSTRACT FROM AUTHOR]