| Autor: |
Shu, Xinyue, Yin, Desuo, Liang, Juan, Xiang, Ting, Zhang, Chao, Li, Honglian, Zheng, Aiping, Li, Ping, Wang, Aijun |
| Předmět: |
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| Zdroj: |
Plant, Cell & Environment; Jul2024, Vol. 47 Issue 7, p2459-2474, 16p |
| Abstrakt: |
Tilletia horrida is an important soilborne fungal pathogen that causes rice kernel smut worldwide. We found a glycoside hydrolase family 128 protein, designated ThGhd_7, caused cell death in Nicotiana benthamiana leaves. The predicted signal peptide (SP) of ThGhd_7 targets it for secretion. However, loss of the SP did not affect its ability to induce cell death. The 23–201 amino acid sequence of ThGhd_7 was sufficient to trigger cell death in N. benthamiana. ThGhd_7 expression was induced and upregulated during T. horrida infection. ThGhd_7 localised to both the cytoplasm and nucleus of plant cells, and nuclear localisation was required to induce cell death. The ability of ThGhd_7 to trigger cell death in N. benthamiana depends on RAR1 (required for Mla12 resistance), SGT1 (suppressor of G2 allele of Skp1), and BAK1/SERK3 (somatic embryogenesis receptor‐like kinase 3). Heterologous overexpression of ThGhd_7 in rice reduced reactive oxygen species (ROS) production and enhanced susceptibility to T. horrida. Further research revealed that ThGhd_7 interacted with and destabilised OsSGT1, which is required for ROS production and is a positive regulator of rice resistance to T. horrida. Taken together, these findings suggest that T. horrida employs ThGhd_7 to disrupt ROS production and thereby promote infection. Summary Statement: Tilletia horrida is an important soilborne fungal pathogen that causes rice kernel smut (RKS) worldwide. This article finds that glycoside hydrolase family 128 protein ThGhd_7 suppressed host immune responses and thereby promoted T. horrida infection by modulating OsSGT1‐mediated reactive oxygen species (ROS) production. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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