Ca2+-dependent H2O2 response in roots and leaves of barley - a transcriptomic investigation

被引:0
|
作者
Bhattacharyya, Sabarna [1 ]
Bleker, Carissa [2 ]
Meier, Bastian [3 ]
Giridhar, Maya [4 ]
Rodriguez, Elena Ulland [1 ]
Braun, Adrian Maximilian [1 ]
Peiter, Edgar [3 ]
Vothknecht, Ute C. [1 ]
Chigri, Fatima [1 ]
机构
[1] Univ Bonn, Inst Cellular & Mol Bot IZMB, Kirschallee 1, D-53115 Bonn, Germany
[2] Natl Inst Biol NIB, Dept Biotechnol & Syst Biol, Vecna Pot 111, Ljubljana SI-1000, Slovenia
[3] Martin Luther Univ Halle Wittenberg, Inst Agr & Nutr Sci, Fac Nat Sci 3, Betty Heimann Str 3, D-06120 Halle An Der Saale, Germany
[4] Tech Univ Munich, Leibniz Inst Food Syst Biol, Lise Meitner Str 34, D-85354 Freising Weihenstephan, Germany
来源
BMC PLANT BIOLOGY | 2025年 / 25卷 / 01期
关键词
ROS; Stress; RNA-Seq; Ca2+ signaling; Crosstalk; Hordeum vulgare; HYDROGEN-PEROXIDE SENSOR; INDUCED OXIDATIVE STRESS; ARABIDOPSIS-THALIANA; GENE-EXPRESSION; SIGNALING PATHWAYS; PROTEIN-KINASES; NADPH OXIDASE; NITRIC-OXIDE; K-MEANS; CALCIUM;
D O I
10.1186/s12870-025-06248-9
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background Ca2+ and H2O2 are second messengers that regulate a wide range of cellular events in response to different environmental and developmental cues. In plants, stress-induced H2O2 has been shown to initiate characteristic Ca2+ signatures; however, a clear picture of the molecular connection between H2O2-induced Ca2+ signals and H2O2-induced cellular responses is missing, particularly in cereal crops such as barley. Here, we employed RNA-seq analyses to identify transcriptome changes in roots and leaves of barley after H2O2 treatment under conditions that inhibited the formation of cytosolic Ca2+ transients. To that end, plasma membrane Ca2+ channels were blocked by LaCl3 application prior to stimulation of barley tissues with H2O2. Results We examined the expression patterns of 4246 genes that had previously been shown to be differentially expressed upon H2O2 application. Here, we further compared their expression between H2O2 and LaCl3 + H2O2 treatment. Genes showing expression patterns different to the previous study were considered to be Ca2+-dependent H2O2-responsive genes. These genes, numbering 331 in leaves and 1320 in roots, could be classified in five and four clusters, respectively. Expression patterns of several genes from each cluster were confirmed by RT-qPCR. We furthermore performed a network analysis to identify potential regulatory paths from known Ca2+-related genes to the newly identified Ca2+-dependent H2O2 responsive genes, using the recently described Stress Knowledge Map. This analysis indicated several transcription factors as key points of the responses mediated by the cross-talk between H2O2 and Ca2+. Conclusion Our study indicates that about 70% of the H2O2-responsive genes in barley roots require a transient increase in cytosolic Ca2+ concentrations for alteration in their transcript abundance, whereas in leaves, the Ca2+ dependency was much lower at about 33%. Targeted gene analysis and pathway modeling identified not only known components of the Ca2+ signaling cascade in plants but also genes that are not yet connected to stimuli-associated signaling. Potential key transcription factors identified in this study can be further analyzed in barley and other crops to ultimately disentangle the underlying mechanisms of H2O2-associated signal transduction mechanisms. This could aid breeding for improved stress resistance to optimize performance and productivity under increasing climate challenges.
引用
收藏
页数:23
相关论文
共 50 条
  • [1] H2O2 in plant peroxisomes: an in vivo analysis uncovers a Ca2+-dependent scavenging system
    Costa, Alex
    Drago, Ilaria
    Behera, Smrutisanjita
    Zottini, Michela
    Pizzo, Paola
    Schroeder, Julian I.
    Pozzan, Tullio
    Lo Schiavo, Fiorella
    PLANT JOURNAL, 2010, 62 (05): : 760 - 772
  • [2] Sensitivity of Barley Leaves and Roots to Fusaric Acid, but not to H2O2, Is Associated with Susceptibility to Fusarium Infections
    Barna, Balazs
    Jansen, Carin
    Kogel, Karl-Heinz
    JOURNAL OF PHYTOPATHOLOGY, 2011, 159 (11-12) : 720 - 725
  • [3] H2O2 INJURY CAUSES CA2+-DEPENDENT AND CA-2+-INDEPENDENT HYDROLYSIS OF PHOSPHATIDYLCHOLINE IN ALVEOLAR EPITHELIAL-CELLS
    RICE, KL
    DUANE, PG
    ARCHER, SL
    GILBOE, DP
    NIEWOEHNER, DE
    AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (04): : L430 - L438
  • [4] Ca2+-dependent cytotoxicity of H2O2 in L929 cells:: The role of H2O2-induced Na+-influx
    Jussofie, A
    Kirsch, M
    de Groot, H
    FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (06) : 712 - 719
  • [5] Histochemical detection of H2O2 and O2- in barley leaves infected with Cochliobolus sativus
    Silva, P.
    Rodriguez, S.
    Torres Puyo, C.
    Gamba, F.
    Pritsch, C.
    PHYTOPATHOLOGY, 2010, 100 (06) : S118 - S118
  • [6] Glucose oxidase-produced H2O2 induces Ca2+-dependent DNA damage in human peripheral blood lymphocytes
    Panayiotidis, R
    Tsolas, O
    Galaris, D
    FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (5-6) : 548 - 556
  • [7] Induction of endothelial nitric oxide synthase expression by H2O2:: Role for a Ca2+-dependent, herbimycin A-sensitive signalling pathway
    Cai, H
    Drummond, GR
    Davis, ME
    Ramasamy, S
    Harrison, DG
    CIRCULATION, 1999, 100 (18) : 480 - 480
  • [8] Identification of an H2O2 permeable PIP aquaporin in barley and a serine residue promoting H2O2 transport
    Rhee, Jiye
    Horie, Tomoaki
    Sasano, Shizuka
    Nakahara, Yoshiki
    Katsuhara, Maki
    PHYSIOLOGIA PLANTARUM, 2017, 159 (01) : 120 - 128
  • [9] CA2+ REGULATION OF THYROID NADPH-DEPENDENT H2O2 GENERATION
    DUPUY, C
    DEME, D
    KANIEWSKI, J
    POMMIER, J
    VIRION, A
    FEBS LETTERS, 1988, 233 (01) : 74 - 78
  • [10] Osmotic stress decreases PIP aquaporin transcripts in barley roots but H2O2 is not involved in this process
    Katsuhara, Maki
    Tsuji, Nobuya
    Shibasaka, Mineo
    Panda, Sanjib Kumar
    JOURNAL OF PLANT RESEARCH, 2014, 127 (06) : 787 - 792