Duplication and neofunctionalization of a horizontally transferred xyloglucanase as a facet of the Red Queen coevolutionary dynamic

Author:

Attah Victoria1,Milner David S.1ORCID,Fang Yufeng2ORCID,Yan Xia3ORCID,Leonard Guy1ORCID,Heitman Joseph2ORCID,Talbot Nicholas J.3ORCID,Richards Thomas A.1ORCID

Affiliation:

1. Department of Biology, University of Oxford, Oxford OX1 3SZ, United Kingdom

2. Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710

3. The Sainsbury Laboratory, University of East Anglia, Norwich Research Park NR4 7UH, United Kingdom

Abstract

Oomycete protists share phenotypic similarities with fungi, including the ability to cause plant diseases, but branch in a distant region of the tree of life. It has been suggested that multiple horizontal gene transfers (HGTs) from fungi-to-oomycetes contributed to the evolution of plant-pathogenic traits. These HGTs are predicted to include secreted proteins that degrade plant cell walls, a barrier to pathogen invasion and a rich source of carbohydrates. Using a combination of phylogenomics and functional assays, we investigate the diversification of a horizontally transferred xyloglucanase gene family in the model oomycete species Phytophthora sojae . Our analyses detect 11 xyloglucanase paralogs retained in P. sojae . Using heterologous expression in yeast, we show consistent evidence that eight of these paralogs have xyloglucanase function, including variants with distinct protein characteristics, such as a long-disordered C-terminal extension that can increase xyloglucanase activity. The functional variants analyzed subtend a phylogenetic node close to the fungi-to-oomycete transfer, suggesting the horizontally transferred gene was a bona fide xyloglucanase. Expression of three xyloglucanase paralogs in Nicotiana benthamiana triggers high-reactive oxygen species (ROS) generation, while others inhibit ROS responses to bacterial immunogens, demonstrating that the paralogs differentially stimulate pattern-triggered immunity. Mass spectrometry of detectable enzymatic products demonstrates that some paralogs catalyze the production of variant breakdown profiles, suggesting that secretion of variant xyloglucanases increases efficiency of xyloglucan breakdown as well as diversifying the damage-associated molecular patterns released. We suggest that this pattern of neofunctionalization and the variant host responses represent an aspect of the Red Queen host–pathogen coevolutionary dynamic.

Funder

Leverhulme Trust

Royal Society

Publisher

Proceedings of the National Academy of Sciences

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