4.7 Article

Brassinosteroids play multiple roles in nodulation of pea via interactions with ethylene and auxin

期刊

PLANTA
卷 252, 期 4, 页码 -

出版社

SPRINGER
DOI: 10.1007/s00425-020-03478-z

关键词

Auxin; Brassinosteroid; Ethylene; Nodulation; Nitrogen fixation; Pea

资金

  1. Australian Research Council Future Fellowship [FT140100770]
  2. Australian Research Council [DP140101709]
  3. Tasmania Graduate Research Scholarship
  4. Australian Research Council [FT140100770] Funding Source: Australian Research Council

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Main conclusion A comprehensive analysis of the role of brassinosteroids in nodulation, including their interactions with auxin and ethylene revealed that brassinosteroids inhibit infection, promote nodule initiation but do not influence nodule organogenesis or function. Nodulation, the symbiosis between legumes and rhizobial bacteria, is regulated by a suite of hormones including brassinosteroids. Previous studies have found that brassinosteroids promote nodule number by inhibiting ethylene biosynthesis. In this study, we examined the influence of brassinosteroids on the various stages of infection and nodule development. We utilise pea mutants, including brassinosteroid mutantslk,lkaandlkb,the ethylene insensitiveein2mutant and thelk ein2double mutant, along with transgenic lines expressing theDR5::GUS auxin activity marker to investigate how brassinosteroids interact with ethylene and auxin during nodulation. We show that brassinosteroids inhibit the early stages of nodulation, including auxin accumulation, root hair deformation and infection thread formation, and demonstrate that infection thread formation is regulated by brassinosteroids in an ethylene independent manner. In contrast, brassinosteroids appear to act as promoters of nodule initiation through both an ethylene dependent and independent pathway. Although brassinosteroids positively influence the ultimate number of nodules formed, we found that brassinosteroid-deficiency did not influence nodule structure including the vascular pattern of auxin activity or nitrogen-fixation capacity. These findings suggest that brassinosteroids are negative regulators of infection but positive regulators of nodule initiation. Furthermore, brassinosteroids do not appear to be essential for nodule organogenesis or function. Given the influence of brassinosteroids on discreet stages of nodulation but not nodule function, manipulation of brassinosteroids may be an interesting avenue for future research on the optimisation of nodulation.

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