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The maize heterotrimeric G-protein β subunit controls shoot meristem development and immune responses.

By Qingyu Wu, Fang Xu, Lei Liu, Si Nian Char, Yezhang Ding, Eric Schmelz, Bing Yang, David Jackson

Posted 08 Oct 2019
bioRxiv DOI: 10.1101/797985 (published DOI: 10.1073/pnas.1917577116)

Heterotrimeric G-proteins are important transducers of receptor signaling, functioning in plants with CLAVATA receptors in control of shoot meristem size, and with pathogen associated molecular pattern (PAMP) receptors in basal immunity. However, whether specific members of the heterotrimeric complex potentiate crosstalk between development and defense, and the extent to which these functions are conserved across species, has not been addressed. Here we used CRISPR/Cas9 to knockout the maize Gβ subunit gene, and found that the mutants were lethal, differing from Arabidopsis, where homologous mutants have normal growth and fertility. We show that lethality is not caused by a specific developmental arrest, but by autoimmunity. We used a genetic diversity screen to suppress the lethal gβ phenotype, and also identified a new maize Gβ allele with weak autoimmune responses but strong development phenotypes. Using these tools, we show that Gβ controls meristem size in maize, acting epistatically with Gα, suggesting that Gβ and Gα function in a common signaling complex. Furthermore, we used an association study to show that natural variation in Gβ influences maize kernel row number, an important agronomic trait. Our results demonstrate the dual role of Gβ in immunity and development in a cereal crop, and suggest that it functions in crosstalk between these competing signaling networks. Therefore, modification of Gβ has the potential to optimize the tradeoff between growth and defense signaling to improve agronomic production.

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