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A protein complex required for polar growth of rhizobial infection threads

Author

Listed:
  • Cheng-Wu Liu

    (Cell and Developmental Biology, John Innes Centre
    University of Cambridge)

  • Andrew Breakspear

    (Cell and Developmental Biology, John Innes Centre)

  • Nicola Stacey

    (Cell and Developmental Biology, John Innes Centre)

  • Kim Findlay

    (Cell and Developmental Biology, John Innes Centre)

  • Jin Nakashima

    (Noble Research Institute)

  • Karunakaran Ramakrishnan

    (Cell and Developmental Biology, John Innes Centre)

  • Miaoxia Liu

    (Chinese Academy of Sciences)

  • Fang Xie

    (Chinese Academy of Sciences)

  • Gabriella Endre

    (Institute of Plant Biology, Biological Research Centre)

  • Fernanda Carvalho-Niebel

    (LIPM, Université de Toulouse, INRA, CNRS)

  • Giles E. D. Oldroyd

    (University of Cambridge)

  • Michael K. Udvardi

    (Noble Research Institute)

  • Joëlle Fournier

    (LIPM, Université de Toulouse, INRA, CNRS)

  • Jeremy D. Murray

    (Cell and Developmental Biology, John Innes Centre
    Institute of Plant Physiology and Ecology, Chinese Academy of Sciences)

Abstract

During root nodule symbiosis, intracellular accommodation of rhizobia by legumes is a prerequisite for nitrogen fixation. For many legumes, rhizobial colonization initiates in root hairs through transcellular infection threads. In Medicago truncatula, VAPYRIN (VPY) and a putative E3 ligase LUMPY INFECTIONS (LIN) are required for infection thread development but their cellular and molecular roles are obscure. Here we show that LIN and its homolog LIN-LIKE interact with VPY and VPY-LIKE in a subcellular complex localized to puncta both at the tip of the growing infection thread and at the nuclear periphery in root hairs and that the punctate accumulation of VPY is positively regulated by LIN. We also show that an otherwise nuclear and cytoplasmic exocyst subunit, EXO70H4, systematically co-localizes with VPY and LIN during rhizobial infection. Genetic analysis shows that defective rhizobial infection in exo70h4 is similar to that in vpy and lin. Our results indicate that VPY, LIN and EXO70H4 are part of the symbiosis-specific machinery required for polar growth of infection threads.

Suggested Citation

  • Cheng-Wu Liu & Andrew Breakspear & Nicola Stacey & Kim Findlay & Jin Nakashima & Karunakaran Ramakrishnan & Miaoxia Liu & Fang Xie & Gabriella Endre & Fernanda Carvalho-Niebel & Giles E. D. Oldroyd & , 2019. "A protein complex required for polar growth of rhizobial infection threads," Nature Communications, Nature, vol. 10(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10029-y
    DOI: 10.1038/s41467-019-10029-y
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    Cited by:

    1. Penelope L. Lindsay & Sergey Ivanov & Nathan Pumplin & Xinchun Zhang & Maria J. Harrison, 2022. "Distinct ankyrin repeat subdomains control VAPYRIN locations and intracellular accommodation functions during arbuscular mycorrhizal symbiosis," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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