# Disruption of CmHmgr1 triggers apoptosis and causes defects in growth, conidiogenesis, and mycoparasitism of Coniothyrium minitans

**Authors:** Xiaoxiang Yang, Haixuan Wang, Lei Zhang, Zhongmei Zhang, Zijin Hu, Daohong Jiang, Yanping Fu

PMC · DOI: 10.1080/21505594.2025.2523884 · 2025-07-23

## TL;DR

Disrupting the CmHmgr1 gene in Coniothyrium minitans impairs its growth, spore production, and ability to parasitize other fungi.

## Contribution

This study identifies CmHmgr1 as a key gene involved in conidiogenesis and mycoparasitism in C. minitans.

## Key findings

- Disruption of CmHmgr1 leads to reduced hyphal development and conidiation in C. minitans.
- CmHmgr1 is localized in mitochondria and its disruption triggers apoptosis.
- The gene is essential for effective mycoparasitism of Sclerotinia sclerotiorum by C. minitans.

## Abstract

Coniothyrium minitans is a well-known mycoparasite against Sclerotinia sclerotiorum. Two critical factors for the commercialization of C. minitans as a biocontrol agent are conidial production and parasitism. To decipher the mechanisms of conidiogenesis and mycoparasitism in C. minitans, a conidiation-deficient mutant, ZS-1TN5012, was isolated from a transfer DNA (T-DNA) insertional library. This mutant exhibited significantly reduced hyphal development, poor conidiation, and decreased sclerotial mycoparasitism. CmHmgr1 encoding a 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) was disrupted by the T-DNA insertion. The colony morphology of the wild-type strain ZS-1 resembled that of the mutant ZS-1TN5012 when the HMGR inhibitor atorvastatin was added to potato dextrose agar, with the mutant showing more sensitivity to atorvastatin. Furthermore, cellular localization assays revealed that CmHmgr1 was localized in mitochondria. Gene replacement and complementation experiments confirmed that CmHmgr1 is involved in the growth, conidiogenesis and mycoparasitism of C. minitans, and disruption of CmHmgr1 triggers apoptosis.

## Linked entities

- **Proteins:** HMGA1 (high mobility group AT-hook 1)
- **Chemicals:** atorvastatin (PubChem CID 60823)
- **Species:** Sclerotinia sclerotiorum (taxon 5180)

## Full-text entities

- **Chemicals:** atorvastatin (MESH:D000069059), agar (MESH:D000362), potato dextrose (-)
- **Species:** Sclerotinia sclerotiorum (species) [taxon 5180], Paraphaeosphaeria minitans (species) [taxon 565426]
- **Cell lines:** ZS-1TN5012 — Homo sapiens (Human), Cockayne syndrome type A, Finite cell line (CVCL_0J83), ZS-1 — Gallus gallus (Chicken), Spontaneously immortalized cell line (CVCL_9R46)

## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12296070/full.md

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Source: https://tomesphere.com/paper/PMC12296070