A role for SPEECHLESS in the integration of leaf stomatal patterning with the growth vs disease trade‐off in poplar. Issue 4 (11th July 2019)

• Record Type: Journal Article
• Authors: McKown, Athena D.; Klápště, Jaroslav; Guy, Robert D.; Corea, Oliver R. A.; Fritsche, Steffi; Ehlting, Jürgen; El‐Kassaby, Yousry A.; Mansfield, Shawn D.
• Is Part Of: New phytologist. Volume 223:Issue 4(2019)
• Page Start: 1888
• Page End: 1903
• Publication Date: 2019-07-11
• Subjects: amphistomaty -- association genetics -- GWAS -- immunity -- Populus trichocarpa -- stomata -- trait trade‐offs; Botany -- Periodicals; 580
• DOI: 10.1111/nph.15911
• Languages: English
• ISSNs: 0028-646X

Abstract

Summary: Occurrence of stomata on both leaf surfaces (amphistomaty) promotes higher stomatal conductance and photosynthesis while simultaneously increasing exposure to potential disease agents in black cottonwood ( Populus trichocarpa ). A genome‐wide association study (GWAS) with 2.2M single nucleotide polymorphisms generated through whole‐genome sequencing found 280 loci associated with variation in adaxial stomatal traits, implicating genes regulating stomatal development and behavior. Strikingly, numerous loci regulating plant growth and response to biotic and abiotic stresses were also identified. The most significant locus was a poplar homologue of SPEECHLESS ( PtSPCH1 ). Individuals possessing PtSPCH1 alleles associated with greater adaxial stomatal density originated primarily from environments with shorter growing seasons (e.g. northern latitudes, high elevations) or with less precipitation. PtSPCH1 was expressed in developing leaves but not developing stem xylem. In developing leaves, RNA sequencing showed patterns of coordinated expression between PtSPCH1 and other GWAS‐identified genes. The breadth of our GWAS results suggests that the evolution of amphistomaty is part of a larger, complex response in plants. Suites of genes underpin this response, retrieved through genetic association to adaxial stomata, and show coordinated expression during development. We propose that the occurrence of amphistomaty in P. trichocarpa involves PtSPCH1 and reflects selection for supporting rapid growth over investment in immunity.