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    Home > Biochemistry News > Biotechnology News > The research team of the Institute of Microbiology revealed the molecular and cellular mechanism by which the kinesin nKCBP regulates symbiosis in rhizobia

    The research team of the Institute of Microbiology revealed the molecular and cellular mechanism by which the kinesin nKCBP regulates symbiosis in rhizobia

    • Last Update: 2022-11-04
    • Source: Internet
    • Author: User
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    On November 1, 2022, the Kong Zhaosheng research group of the Institute of Microbiology published a publication in Nature Plants entitled " A Legume Kinesin Controls Vacuole Morphogenesis for Rhizobia Endosymbiosis", revealing the molecular and cellular mechanism by which the kinesin nKCBP regulates symbiosis in rhizobia

              KCBP (Kinesin-like Calmodulin-Binding Protein) is a unique microtubule motor protein of plants, which has the ability to bind microtubules and microfilaments at the same time, and regulate the dynamic remodeling of the cytoskeleton and the construction of
    cell morphology.
    The KCBP gene doubled in legumes, and the copy nKCBP enriched in nodules evolved to regulate nodular nitrogen
    fixation.
    Tribulus terrestris
    (Medicago truncatula) nkcbp mutant was obtained using gene editing techniques, showing growth defects (Figure 1a) and a significant decrease in nitrogen fixation capacity (Figure 1b).

    Further observation of semi-thin and ultra-thin sections of nodules showed that the infected cells of wild-type nodules had typical large central vacuoles (Figures
    1C and 2A), while NKCBP mutants contained a large number of randomly distributed small, unfused vacuoles (Fig 1d and 2b), and even some infected intracellular symbionts cannot be differentiated, and the symbiont membrane is thickened
    .
    Using
    Automatic collector of ultrathin sections scanning electron microscopy (AutoCUTS-SEM) technology, the structure of wild-type and mutant vacuoles was three-dimensionally reconstructed (Figure 2).

    。 Combined with live-cell imaging and immunofluorescence staining,
    nKCBP has conserved biochemical functions while binding microtubules and microfilaments
    .
    It was further found that compared with the wild type, the
    cytoskeletal radial arrangement in NKCBP mutant infected cells was disrupted and showed a random and disordered arrangement pattern
    .
    In summary,
    nKCBP regulates vacuolegenesis and symbiotic interface formation by regulating cytoskeletal dynamic remodeling (Figure 3), thereby controlling intraneosis and efficient nitrogen fixation in rhizobia.

        

    Figure 1: NKCBP mutant growth phenotype and symbiotic phenotypic analysis

     

     

    Figure 2: Three-dimensional structure of wild-type and NKCBP mutant vacuoles

     

    Figure 3: Working model of nKCBP to control endomorphosis and efficient nitrogen fixation by regulating the dynamic remodeling of the cytoskeleton to regulate vacuolegenesis and symbiotic interface formation

      

             Zhang Xiaxia, assistant researcher of the Institute of Microbiology, Chinese Academy of Sciences, is the first author of the paper, and researcher Kong Zhaosheng, Institute of Microbiology, Chinese Academy of Sciences/Shanxi Agricultural University, is the corresponding author
    .
    Prof.
    Yongbiao Xue from the Institute of Genetics and Developmental Biology of the Chinese Academy of Sciences, Prof.
    Yijing Zhang from the Center for Excellence in Molecular Plant Sciences, CAS, Prof.
    Dong Wang from the University of Massachusetts, Prof.
    Youguo Li and Associate Prof.
    Dasong Chen from Huazhong Agricultural University also participated in the study
    .
     

    This research was supported
    by the National Science Foundation for Outstanding Young Scholars, the Strategic Leading Science and Technology Special Program of the Chinese Academy of Sciences, the Young Team Program in Basic Research Fields, and the independent research project of the State Key Laboratory of Plant Genomics.

    Related paper information: https://doi.
    org/10.
    1038/s41477-022-01261-4
     

     

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