Competence for transcellular infection in the root cortex involves a post-replicative, cell-cycle exit decision in Medicago truncatula

During root nodule symbiosis (RNS), cell-division activity is reinitiated and sustained in the root cortex to create a hospitable cellular niche. Such a temporary and spatially confined site is required to render host cells compatible with the intracellular progression of rhizobia. Although it has b...

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Main Authors: Morgane Batzenschlager, Beatrice Lace, Ning Zhang, Chao Su, Anna Boiger, Sabrina Egli, Pascal Krohn, Jule Salfeld, Franck Anicet Ditengou, Thomas Laux, Thomas Ott
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2025-07-01
Series:eLife
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Online Access:https://elifesciences.org/articles/88588
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Summary:During root nodule symbiosis (RNS), cell-division activity is reinitiated and sustained in the root cortex to create a hospitable cellular niche. Such a temporary and spatially confined site is required to render host cells compatible with the intracellular progression of rhizobia. Although it has been suggested that early infection events might involve a pre-mitotic cell-cycle arrest, this process has not been dissected with cellular resolution. Here, we show that a dual-color Medicago histone reporter robustly identifies cells with different mitotic or endoreduplication activities in the root cortex. By imaging deep root tissues, we found that a confined trajectory of cortical cells that are transcellularly passed by infection threads is in a stage of the cell cycle that is distinct from directly adjacent cells. Distinctive features of infected cells include nuclear widening and large-scale chromatin rearrangements consistent with a cell-cycle exit prior to differentiation. Using a combination of fluorescent reporters demarcating cell-cycle phase progression, we confirmed that a reduced proliferation potential and modulating the G2/M transition, a process possibly controlled by the NF-YA1 transcription factor, mark the success of rhizobial delivery to nodule cells.
ISSN:2050-084X