4.8 Article

Heterotrimeric G-Protein Interactions Are Conserved Despite Regulatory Element Loss in Some Plants

Journal

PLANT PHYSIOLOGY
Volume 184, Issue 4, Pages 1941-1954

Publisher

AMER SOC PLANT BIOLOGISTS
DOI: 10.1104/pp.20.01309

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Funding

  1. National Science Foundation [MCB-1714693, IOS-1557942]

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The functional networks between the G-protein alpha -subunit and its regulatory protein, RGS, are conserved in plants, and despite the absence of RGS in many monocots, their corresponding G alpha proteins have retained the ability to be deactivated by nonnative RGS in planta. Heterotrimeric G-proteins are key modulators of multiple signaling and development pathways in plants and regulate many agronomic traits, including architecture and grain yield. Regulator of G-protein signaling (RGS) proteins are an integral part of the G-protein networks; however, these are lost in many monocots. To assess if the loss of RGS in specific plants has resulted in altered G-protein networks and the extent to which RGS function is conserved across contrasting monocots, we explored G-protein-dependent developmental pathways in Brachypodium distachyon and Setaria viridis, representing species without or with a native RGS, respectively. Artificial microRNA-based suppression of G alpha in both species resulted in similar phenotypes. Moreover, overexpression of Setaria italica RGS in B. distachyon resulted in phenotypes similar to the suppression of BdG alpha. This effect of RGS overexpression depended on its ability to deactivate G alpha, as overexpression of a biochemically inactive variant protein resulted in plants indistinguishable from the wild type. Comparative transcriptome analysis of B. distachyon plants with suppressed levels of G alpha or overexpression of RGS showed significant overlap of differentially regulated genes, corroborating the phenotypic data. These results suggest that despite the loss of RGS in many monocots, the G-protein functional networks are maintained, and G alpha proteins have retained their ability to be deactivated by RGS.

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