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タイトル: An atypical NLR protein modulates the NRC immune receptor network in Nicotiana benthamiana
著者: Adachi, Hiroaki
Sakai, Toshiyuki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-2737-3299 (unconfirmed)
Harant, Adeline
Pai, Hsuan
Honda, Kodai
Toghani, AmirAli
Claeys, Jules
Duggan, Cian
Bozkurt, Tolga O
Wu, Chih-Hang
Kamoun, Sophien
著者名の別形: 安達, 広明
堺, 俊之
本田, 晃大
キーワード: Cell death
Nicotiana
Leaves
Sequence motif analysis
Gene silencing
Phylogenetic analysis
Solanum
Immune receptors
発行日: Jan-2023
出版者: Public Library of Science (PLoS)
誌名: PLOS Genetics
巻: 19
号: 1
論文番号: e1010500
抄録: The NRC immune receptor network has evolved in asterid plants from a pair of linked genes into a genetically dispersed and phylogenetically structured network of sensor and helper NLR (nucleotide-binding domain and leucine-rich repeat-containing) proteins. In some species, such as the model plant Nicotiana benthamiana and other Solanaceae, the NRC (NLR-REQUIRED FOR CELL DEATH) network forms up to half of the NLRome, and NRCs are scattered throughout the genome in gene clusters of varying complexities. Here, we describe NRCX, an atypical member of the NRC family that lacks canonical features of these NLR helper proteins, such as a functional N-terminal MADA motif and the capacity to trigger autoimmunity. In contrast to other NRCs, systemic gene silencing of NRCX in N. benthamiana markedly impairs plant growth resulting in a dwarf phenotype. Remarkably, dwarfism of NRCX silenced plants is partially dependent on NRCX paralogs NRC2 and NRC3, but not NRC4. Despite its negative impact on plant growth when silenced systemically, spot gene silencing of NRCX in mature N. benthamiana leaves doesn’t result in visible cell death phenotypes. However, alteration of NRCX expression modulates the hypersensitive response mediated by NRC2 and NRC3 in a manner consistent with a negative role for NRCX in the NRC network. We conclude that NRCX is an atypical member of the NRC network that has evolved to contribute to the homeostasis of this genetically unlinked NLR network.
著作権等: © 2023 Adachi et al.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
URI: http://hdl.handle.net/2433/278959
DOI(出版社版): 10.1371/journal.pgen.1010500
PubMed ID: 36656829
出現コレクション:学術雑誌掲載論文等

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