CRISPR/Cas9 disruption of UGT71L1 in poplar connects salicinoid and salicylic acid metabolism and alters growth and morphology

Author:

Gordon Harley1ORCID,Fellenberg Christin1ORCID,Lackus Nathalie D2ORCID,Archinuk Finn1ORCID,Sproule Amanda3,Nakamura Yoko45ORCID,K�llner Tobias G2ORCID,Gershenzon Jonathan2ORCID,Overy David P3ORCID,Constabel C Peter1ORCID

Affiliation:

1. Department of Biology, Centre for Forest Biology, University of Victoria , Victoria, BC V8P 5C2, Canada

2. Department of Biochemistry, Max Planck Institute for Chemical Ecology , Jena 07745, Germany

3. Agriculture and Agri-Food Canada , Ottawa, Ontario K1A 0C6, Canada

4. Department of Nuclear Magnetic Resonance, Max Planck Institute for Chemical Ecology , Jena 07745, Germany

5. Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology , Jena 07745, Germany

Abstract

Abstract Salicinoids are salicyl alcohol-containing phenolic glycosides with strong antiherbivore effects found only in poplars and willows. Their biosynthesis is poorly understood, but recently a UDP-dependent glycosyltransferase, UGT71L1, was shown to be required for salicinoid biosynthesis in poplar tissue cultures. UGT71L1 specifically glycosylates salicyl benzoate, a proposed salicinoid intermediate. Here, we analyzed transgenic CRISPR/Cas9-generated UGT71L1 knockout plants. Metabolomic analyses revealed substantial reductions in the major salicinoids, confirming the central role of the enzyme in salicinoid biosynthesis. Correspondingly, UGT71L1 knockouts were preferred to wild-type by white-marked tussock moth (Orgyia leucostigma) larvae in bioassays. Greenhouse-grown knockout plants showed substantial growth alterations, with decreased internode length and smaller serrated leaves. Reinserting a functional UGT71L1 gene in a transgenic rescue experiment demonstrated that these effects were due only to the loss of UGT71L1. The knockouts contained elevated salicylate (SA) and jasmonate (JA) concentrations, and also had enhanced expression of SA- and JA-related genes. SA is predicted to be released by UGT71L1 disruption, if salicyl salicylate is a pathway intermediate and UGT71L1 substrate. This idea was supported by showing that salicyl salicylate can be glucosylated by recombinant UGT71L1, providing a potential link of salicinoid metabolism to SA and growth impacts. Connecting this pathway with growth could imply that salicinoids are under additional evolutionary constraints beyond selective pressure by herbivores.

Funder

Natural Science and Engineering Research Council of Canada, Agriculture and Agri-food Canada

Max-Planck Society

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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