4.7 Article

Defining the Cell Wall, Cell Cycle and Chromatin Landmarks in the Responses of Brachypodium distachyon to Salinity

Journal

Publisher

MDPI
DOI: 10.3390/ijms22020949

Keywords

Brachypodium distachyon; cell cycle; epigenetics; germination; replication; salt stress

Funding

  1. National Science Centre, Poland [2015/18/M/NZ2/00394]

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Salt stress affects germination and root growth in Brachypodium, influencing the expression of cell wall expansion-regulating proteins, induction of cell cycle genes, and alterations in genomic and epigenetic mechanisms such as histone acetylation and DNA methylation. These findings suggest a complex molecular response to salt stress in plants, indicating potential avenues for further functional genomics research.
Excess salinity is a major stress that limits crop yields. Here, we used the model grass Brachypodium distachyon (Brachypodium) reference line Bd21 in order to define the key molecular events in the responses to salt during germination. Salt was applied either throughout the germination period (salt stress) or only after root emergence (salt shock). Germination was affected at >= 100 mM and root elongation at >= 75 mM NaCl. The expression of arabinogalactan proteins (AGPs), FLA1, FLA10, FLA11, AGP20 and AGP26, which regulate cell wall expansion (especially FLA11), were mostly induced by the salt stress but to a lesser extent by salt shock. Cytological assessment using two AGP epitopes, JIM8 and JIM13 indicated that salt stress increases the fluorescence signals in rhizodermal and exodermal cell wall. Cell division was suppressed at >75 mM NaCl. The cell cycle genes (CDKB1, CDKB2, CYCA3, CYCB1, WEE1) were induced by salt stress in a concentration-dependent manner but not CDKA, CYCA and CYCLIN-D4-1-RELATED. Under salt shock, the cell cycle genes were optimally expressed at 100 mM NaCl. These changes were consistent with the cell cycle arrest, possibly at the G1 phase. The salt-induced genomic damage was linked with the oxidative events via an increased glutathione accumulation. Histone acetylation and methylation and DNA methylation were visualized by immunofluorescence. Histone H4 acetylation at lysine 5 increased strongly whereas DNA methylation decreased with the application of salt. Taken together, we suggest that salt-induced oxidative stress causes genomic damage but that it also has epigenetic effects, which might modulate the cell cycle and AGP expression gene. Based on these landmarks, we aim to encourage functional genomics studies on the responses of Brachypodium to salt.

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