A Fungal Natural Product that Inhibits Plant Cellulose Biosynthesis by disrupting Cellulose Synthase Complexes

preprint OA: closed CC-BY-4.0
📄 Open PDF Full text JSON View at publisher

Abstract

Cellulose, a primary component of plant cell walls, is synthesized by cellulose synthase complexes (CSCs) at the plasma membrane. Targeting this process with cellulose biosynthesis inhibitors (CBIs) has significantly advanced our understanding of plant cell wall formation and provided valuable compounds for herbicide development. Here, we identified a fungal natural product, 8-methyldichlorodiaporthin (MDD), as a broad-spectrum plant CBI. Structure-activity relationship analyses demonstrate that methylation modifications on the isocoumarin ring and chlorination of side chain are crucial for MDD-induced growth inhibition. A chemical forward genetic screen in Arabidopsis thaliana revealed two semi-dominant CESA1 mutations, causing A903T and H1024Y substitutions, that confer insensitivity to MDD. Both mutations locate to transmembrane domains of CESA1, and we show that MDD depletes CSCs from the plasma membrane and reduces cellulose content. Further genetic analyses indicate that the cesa1 mddi1-1 A903T mutant also confers resistance to CBIs quinoxyphen and C17, but not to CBIs isoxaben, indaziflam, or ES20. Stacking additional point mutations conferring resistance to other CBIs, cesa3 ixr1-1 G998D , and cesa6 es20-r3 G935E into the cesa1 mddi1-1 A903T background yields multiple-drugs resistant lines that maintain normal growth. These findings establish MDD, as a novel, natural CBI that likely targets CESA1, thereby extending our understanding of CSC regulation and abilities to develop multi-drugs resistant crop varieties. These findings offer new perspectives for weed management and plant biotechnology. Significance Statement Cellulose, a fundamental structural component of plant cell walls, is synthesized by cellulose synthase complexes (CSCs) and represents a critical herbicide target. While synthetic cellulose biosynthesis inhibitors (CBIs) like isoxaben and quinoxyphen have helped in the elucidation of CSC function and aided in weed control, natural CBIs remain largely undiscovered. Here, we identify 8-methyldichlorodiaporthin (MDD), a fungal-derived isocoumarin natural product, as a CBI that inhibits plant growth by depleting CSCs from the plasma membrane. Genetic screens reveal MDD-resistant cesa1 mutations, and combining these with other CBI-resistant alleles yields multi-herbicide resistant plants that can grow normally. This research enhances our understanding of cellulose biosynthesis and paves the way for multi-herbicide resistant crops with agricultural benefits.
Full text 2,694 characters · extracted from oa-doi-fallback · click to expand
Abstract Cellulose, a primary component of plant cell walls, is synthesized by cellulose synthase complexes (CSCs) at the plasma membrane. Targeting this process with cellulose biosynthesis inhibitors (CBIs) has significantly advanced our understanding of plant cell wall formation and provided valuable compounds for herbicide development. Here, we identified a fungal natural product, 8-methyldichlorodiaporthin (MDD), as a broad-spectrum plant CBI. Structure-activity relationship analyses demonstrate that methylation modifications on the isocoumarin ring and chlorination of side chain are crucial for MDD-induced growth inhibition. A chemical forward genetic screen in Arabidopsis thaliana revealed two semi-dominant CESA1 mutations, causing A903T and H1024Y substitutions, that confer insensitivity to MDD. Both mutations locate to transmembrane domains of CESA1, and we show that MDD depletes CSCs from the plasma membrane and reduces cellulose content. Further genetic analyses indicate that the cesa1mddi1-1 A903T mutant also confers resistance to CBIs quinoxyphen and C17, but not to CBIs isoxaben, indaziflam, or ES20. Stacking additional point mutations conferring resistance to other CBIs, cesa3ixr1-1 G998D, and cesa6es20-r3 G935E into the cesa1mddi1-1 A903T background yields multiple-drugs resistant lines that maintain normal growth. These findings establish MDD, as a novel, natural CBI that likely targets CESA1, thereby extending our understanding of CSC regulation and abilities to develop multi-drugs resistant crop varieties. These findings offer new perspectives for weed management and plant biotechnology. Significance Statement Cellulose, a fundamental structural component of plant cell walls, is synthesized by cellulose synthase complexes (CSCs) and represents a critical herbicide target. While synthetic cellulose biosynthesis inhibitors (CBIs) like isoxaben and quinoxyphen have helped in the elucidation of CSC function and aided in weed control, natural CBIs remain largely undiscovered. Here, we identify 8-methyldichlorodiaporthin (MDD), a fungal-derived isocoumarin natural product, as a CBI that inhibits plant growth by depleting CSCs from the plasma membrane. Genetic screens reveal MDD-resistant cesa1 mutations, and combining these with other CBI-resistant alleles yields multi-herbicide resistant plants that can grow normally. This research enhances our understanding of cellulose biosynthesis and paves the way for multi-herbicide resistant crops with agricultural benefits. Competing Interest Statement The authors have declared no competing interest. Footnotes Competing Interest Statement: Authors declare that they have no competing interests.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2026) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-06-04T02:00:05.705006+00:00
License: CC-BY-4.0