GhPME36 aggravates susceptibility to Liriomyza sativae by affecting cell wall biosynthesis in cotton leaves
文献类型: 外文期刊
第一作者: Yang, Zheng
作者: Yang, Zheng;Wang, Menglei;Zhang, Doudou;He, Jie;Li, Tongyi;Wang, Panpan;Yuan, Youlu;Shang, Haihong;Fan, Senmiao;Zhang, Zhen;Wei, Renhui;Li, Weijie;Wang, Lin;Wang, Shaogan;Yuan, Youlu;Shang, Haihong;Yang, Zheng;Dawood, Muhammad;Shang, Haihong;Fan, Senmiao
作者机构:
关键词: PME; Cotton; Liriomyza sativae; Cell wall biosynthesis; Glucose metabolism
期刊名称:BMC BIOLOGY ( 影响因子:4.5; 五年影响因子:5.4 )
ISSN:
年卷期: 2024 年 22 卷 1 期
页码:
收录情况: SCI
摘要: Background Cotton is an important economic crop and a host of Liriomyza sativae. Pectin methylesterase (PME)-mediated pectin metabolism plays an indispensable role in multiple biological processes in planta. However, the pleiotropic functions of PME often lead to unpredictable effects on crop resistance to pests. Additionally, whether and how PME affects susceptibility to Liriomyza sativae remain unclear. Results Here, we isolated GhPME36, which is located in the cell wall, from upland cotton (Gossypium hirsutum L.). Interestingly, the overexpression of GhPME36 in cotton caused severe susceptibility to Liriomyza sativae but increased leaf biomass in Arabidopsis. Cytological observations revealed that the cell wall was thinner with more demethylesterified pectins in GhPME36-OE cotton leaves than in WT leaves, whereas the soluble sugar content of GhPME36-OE cotton leaf cell walls was accordingly higher; both factors attracted Liriomyza sativae to feed on GhPME36-OE cotton leaves. Metabolomic analysis demonstrated that glucose was significantly differentially accumulated. Transcriptomic analysis further revealed DEGs enriched in glucose metabolic pathways when GhPME36 was overexpressed, suggesting that GhPME36 aggravates susceptibility to Liriomyza sativae by affecting both the structure and components of cell wall biosynthesis. Moreover, GhPME36 interacts with another pectin-modifying enzyme, GhC/VIF1, to maintain the dynamic stability of pectin methyl esterification. Conclusions Taken together, our results reveal the cytological and molecular mechanisms by which GhPME36 aggravates susceptibility to Liriomyza sativae. This study broadens the knowledge of PME function and provides new insights into plant resistance to pests and the safety of genetically modified plants.
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