TY - JOUR
T1 - Heterotrimeric G-protein interactions are conserved despite regulatory element loss in some plants
AU - Bhatnagar, Nikita
AU - Pandey, Sona
N1 - Funding Information:
1This work was supported by the National Science Foundation (grant nos. MCB–1714693 and IOS–1557942). 2Author for contact: [email protected]. 3Senior author. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Sona Pandey ([email protected]). S.P. conceived the project; N.B. performed all experiments with input from S.P.; N.B. and S.P. wrote the article. [OPEN]Articles can be viewed without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.20.01309
Publisher Copyright:
© 2020 American Society of Plant Biologists. All Rights Reserved.
PY - 2020/12
Y1 - 2020/12
N2 - 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 Ga in both species resulted in similar phenotypes. Moreover, overexpression of Setaria italica RGS in B. distachyon resulted in phenotypes similar to the suppression of BdGa. This effect of RGS overexpression depended on its ability to deactivate Ga, 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 Ga 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 Ga proteins have retained their ability to be deactivated by RGS.
AB - 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 Ga in both species resulted in similar phenotypes. Moreover, overexpression of Setaria italica RGS in B. distachyon resulted in phenotypes similar to the suppression of BdGa. This effect of RGS overexpression depended on its ability to deactivate Ga, 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 Ga 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 Ga proteins have retained their ability to be deactivated by RGS.
UR - http://www.scopus.com/inward/record.url?scp=85097469602&partnerID=8YFLogxK
U2 - 10.1104/pp.20.01309
DO - 10.1104/pp.20.01309
M3 - Article
C2 - 33082269
AN - SCOPUS:85097469602
SN - 0032-0889
VL - 184
SP - 1941
EP - 1954
JO - Plant Physiology
JF - Plant Physiology
IS - 4
ER -