PbrRALF2-elicited reactive oxygen species signaling is mediated by the PbrCrRLK1L13-PbrMPK18 module in pear pollen tubes

Xiaobing Kou , Jiangmei Sun , Peng Wang , Danqi Wang , Peng Cao , Jing Lin , Youhong Chang , Shaoling Zhang , Juyou Wu

Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) : 222

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Horticulture Research ›› 2021, Vol. 8 ›› Issue (1) :222 DOI: 10.1038/s41438-021-00684-y
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PbrRALF2-elicited reactive oxygen species signaling is mediated by the PbrCrRLK1L13-PbrMPK18 module in pear pollen tubes
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Abstract

Rapid alkalinization factors (RALFs) are cysteine-rich peptides that play important roles in a variety of biological processes, such as cell elongation and immune signaling. Recent studies in Arabidopsis have shown that RALFs regulate pollen tube growth via plasma membrane receptor-like kinases (RLKs). However, the downstream signal transduction mechanisms of RLKs in pollen tubes are unknown. Here, we identified PbrRALF2, a pear (Pyrus bretschneideri) pollen RALF peptide that inhibits pollen tube growth. We found that PbrRALF2 interacts with a malectin-like domain-containing RLK, PbrCrRLK1L13. The relative affinity between PbrRALF2 and PbrCrRLK1L13 was at the submicromolar level, which is consistent with the values of ligand–receptor kinase pairs and the physiological concentration for PbrRALF2-mediated inhibition of pollen tube growth. After binding to its extracellular domain, PbrRALF2 activated the phosphorylation of PbrCrRLK1L13 in a dose-dependent manner. We further showed that the MAP kinase PbrMPK18 is a downstream target of PbrCrRLK1L13 that mediates PbrRALF2-elicited reactive oxygen species (ROS) production. The excessive accumulation of ROS inhibits pollen tube growth. We show that MPK acts as a mediator for CrRLK1L to stimulate ROS production, which might represent a general mechanism by which RALF and CrRLK1L function in signaling pathways.

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Xiaobing Kou, Jiangmei Sun, Peng Wang, Danqi Wang, Peng Cao, Jing Lin, Youhong Chang, Shaoling Zhang, Juyou Wu. PbrRALF2-elicited reactive oxygen species signaling is mediated by the PbrCrRLK1L13-PbrMPK18 module in pear pollen tubes. Horticulture Research, 2021, 8 (1) : 222 DOI:10.1038/s41438-021-00684-y

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References

[1]

Muschietti, J. et al. LAT52 protein is essential for tomato pollen development: pollen expressing antisense LAT52 RNA hydrates and germinates abnormally and cannot achieve fertilization. Plant J. 6, 321-338 (1994).

[2]

Chen, Y. F. et al. Peptide growth factor phytosulfokine-α contributes to the pollen population effect. Planta 211, 752-755 (2000).

[3]

Covey, P. A. et al. A pollen-specific RALF from tomato that regulates pollen tube elongation. Plant Physiol. 153, 703-715 (2010).

[4]

Mecchia, M. A. et al. RALF4/19 peptides interact with LRX proteins to control pollen tube growth in Arabidopsis. Science 358, 1600 (2017).

[5]

Pearce, G. et al. RALF, a 5-kDa ubiquitous polypeptide in plants, arrests root growth and development. Proc. Natl Acad. Sci. USA 98, 12843-12847 (2001).

[6]

Ge, Z. et al. Arabidopsis pollen tube integrity and sperm release are regulated by RALF-mediated signaling. Science 358, 1596 (2017).

[7]

Moussu, S. et al. Structural basis for recognition of RALF peptides by LRX proteins during pollen tube growth. Proc. Natl Acad. Sci. USA 117, 7494-7503 (2020).

[8]

Haruta, M. et al. Peptide hormone and its receptor protein kinase regulate plant cell expansion. Science 343, 408-411 (2014).

[9]

Yu, M. et al. The RALF1-FERONIA interaction modulates endocytosis to mediate control of root growth in Arabidopsis. Development 147, dev.189902 (2020).

[10]

Stegmann, M. et al. The receptor kinase FER is a RALF-regulated scaffold controlling plant immune signaling. Science 355, 287 (2017).

[11]

Duan, Q. et al. FERONIA controls pectin- and nitric oxide-mediated male-female interaction. Nature 579, 7800 (2020).

[12]

Escobar-Restrepo, J. M. et al. The FERONIA receptor-like kinase mediates male-female interactions during pollen tube reception. Science 317, 656-660 (2007).

[13]

Boisson-Dernier, A. et al. Disruption of the pollen-expressed FERONIA homologs ANXUR1 and ANXUR2 triggers pollen tube discharge. Development 136, 3279-3288 (2009).

[14]

Feng, H. et al. LORELEI-LIKE GPI-ANCHORED PROTEINS 2/3 regulate pollen tube growth as chaperones and coreceptors for ANXUR/BUPS receptor kinases in Arabidopsis. Mol. Plant. 12, 1612-1623 (2019).

[15]

Lindner, H. et al. CrRLK1L receptor-like kinases: not just another brick in the wall. Curr. Opin. Plant. Biol. 15, 659-669 (2012).

[16]

Liu, L. et al. Receptor-like kinase RUPO interacts with potassium transporters to regulate pollen tube growth and integrity in Rice. PLoS Genet. 12, e1006085 (2016).

[17]

Miyazaki, S. et al. ANXUR1 and 2, sister genes to FERONIA/SIRENE, are male factors for coordinated fertilization. Curr. Biol. 19, 1327-1331 (2009).

[18]

Nissen, K. S. et al. Understanding CrRLK1L function: cell walls and growth control. Trends Plant Sci. 21, 516-527 (2016).

[19]

Hsi, L. C. et al. Opposing effects of 15-lipoxygenase-1 and -2 metabolites on MAPK signaling in prostate alteration in peroxisome proliferator-activated receptor γ. J. Biol. Chem. 277, 40549-40556 (2002).

[20]

Pece, S. et al. Signaling from e-cadherins to the MAPK pathway by the recruitment and activation of epidermal growth factor receptors upon cell-cell contact formation. J. Biol. Chem. 275, 41227-41233 (2000).

[21]

Li, C. H. et al. The receptor-like kinase SIT1 mediates salt sensitivity by activating MAPK3/6 and regulating ethylene homeostasis in Rice. Plant Cell 26, 2538-2553 (2014).

[22]

Meng, X. et al. A MAPK cascade downstream of ERECTA receptor-like protein kinase regulates Arabidopsis inflorescence architecture by promoting localized cell proliferation. Plant Cell 24, 4948-4960 (2012).

[23]

Kimura, S. et al. Bound by fate: reactive oxygen species in receptor-like kinase signaling. Plant Cell 29, 638-654 (2017).

[24]

Boisson-Dernier, A. et al. ANXUR receptor-like kinases coordinate cell wall integrity with growth at the pollen tube tip via NADPH oxidases. PLoS Biol. 11, e1001719 (2013).

[25]

Chai, L. et al. MAP kinase PrMPK9-1 contributes to the self-incompatibility response. Plant Physiol. 174, 1226-1237 (2017).

[26]

De Graaf, B. et al. Self-incompatibility in Papaver targets soluble inorganic pyrophosphatases in pollen. Nature 444, 490-493 (2006).

[27]

Estruch, J. J. et al. Cloning and characterization of a maize pollen-specific calcium-dependent calmodulin-independent protein kinase. Proc. Nat. Acad. Sci. USA 91, 8837-8841 (1994).

[28]

Meng, D. et al. Decreased sorbitol synthesis leads to abnormal stamen development and reduced pollen tube growth via an MYB transcription factor, MdMYB39L, in apple (Malus domestica). New Phytol. 217, 641-656 (2018).

[29]

Kou, X. et al. Evolution, expression analysis, and functional verification of Catharanthus roseus RLK1-like kinase (CrRLK1L) family proteins in pear (Pyrus bretchneideri). Genomics 109, 290-301 (2017).

[30]

Li, C. et al. FERONIA and her pals: functions and mechanisms. Plant Physiol. 171, 2379-2392 (2016).

[31]

Wang, J. et al. Allosteric receptor activation by the plant peptide hormone phytosulfokine. Nature 525, 265-268 (2016).

[32]

Wu, J. et al. NaRALF, a peptide signal essential for the regulation of root hair tip apoplastic pH in Nicotiana attenuata, is required for root hair development and plant growth in native soils. Plant J. 52, 877-890 (2010).

[33]

Muschietti, J. P. et al. How many receptor-like kinases are required to operate a pollen tube. Curr. Opin. Plant. Biol. 41, 73-82 (2018).

[34]

Brand, U. et al. Dependence of stem cell fate in Arabidopsis on a feedback loop regulated by CLV3 activity. Science 289, 617-619 (2000).

[35]

Galli, M. et al. Expanding the regulatory network for meristem size in plants. Trends Genet. 32, 372-383 (2016).

[36]

Matsubayashi et al. An LRR receptor kinase involved in perception of a peptide plant hormone, Phytosulfokine. Science 296, 1470-1472 (2002).

[37]

Tang, W. A Cysteine-rich extracellular protein, LAT52, interacts with the extracellular domain of the pollen receptor kinase LePRK2. Plant Cell 14, 2277-2287 (2002).

[38]

Takeuchi, H. et al. Tip-localized receptors control pollen tube growth and LURE sensing in Arabidopsis. Nature 531, 245-248 (2016).

[39]

Wang, T. et al. A receptor heteromer mediates the male perception of female attractants in plants. Nature 531, 241-244 (2016).

[40]

Xiao, Y. et al. Mechanisms of RALF peptide perception by a heterotypic receptor complex. Nature 572, 270-274 (2019).

[41]

Dressano, K. et al. BAK1 is involved in AtRALF1-induced inhibition of root cell expansion. PLoS Genet. 13, e1007053 (2017).

[42]

Li, C. et al. Glycosylphosphatidylinositol-anchored proteins as chaperones and co-receptors for FERONIA receptor kinase signaling in Arabidopsis. eLife 4, e06587 (2015).

[43]

Doucet, J. et al. Pollen acceptance or rejection: a tale of two pathways. Trends Plant Sci. 21, 1058-1067 (2016).

[44]

Nasrallah, J. B. Recognition and rejection of self in plant reproduction. Science 296, 305-308 (2002).

[45]

Nasrallah, J. B. Plant mating systems: self-incompatibility and evolutionary transitions to self-fertility in the mustard family. Curr. Opin. Genet Dev. 47, 54 (2017).

[46]

Schopfer, C. R. The male determinant of self-incompatibility in Brassica. Science 286, 1697-1700 (1999).

[47]

Ludwig, A. A. et al. Ethylene-mediated cross-talk between calcium-dependent protein kinase and MAPK signaling controls stress responses in plants. Proc. Nat. Acad. Sci. USA 102, 10736-10741 (2005).

[48]

Moon, H. et al. NDP kinase 2 interacts with two oxidative stress-activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants. Proc. Nat. Acad. Sci. USA 100, 358-363 (2003).

[49]

Takahashi, F. et al. Calmodulin-dependent activation of MAP kinase for ROS homeostasis in Arabidopsis. Mol. Cell 41, 649-660 (2011).

[50]

Kimura, S. et al. CRK2 and c-terminal phosphorylation of NADPH oxidase RBOHD regulate reactive oxygen species production in Arabidopsis. Plant Cell 32, 1063-1080 (2020).

[51]

Forman, H. J. Use and abuse of exogenous H2O2 in studies of signal transduction. Free Radic. Biol. Med. 42, 926-932 (2007).

[52]

Reth, M. Hydrogen peroxide as second messenger in lymphocyte activation. Nat. Immunol. 3, 1129-1134 (2002).

[53]

David, S. G. et al. Laboratory and clinical studies of cancer chemoprevention by antioxidants in berries. Carcinogenesis 29, 1665-1674 (2008).

[54]

Yoo, S. D. et al. Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis. Nat. Protoc. 2, 1565-1572 (2007).

[55]

Livak, K. J. et al. Analysis of relative gene expression data using real-time quantitative PCR. Methods 25, 402-408 (2002).

[56]

Wang, C. L. et al. S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia. J. Cell Sci. 123, 4301-4309 (2011).

[57]

Potocký, M. et al. Reactive oxygen species produced by NADPH oxidase are involved in pollen tube growth. N. Phytol. 174, 742-751 (2007).

[58]

Xie, Q. et al. LNK1 and LNK2 are transcriptional coactivators in the Arabidopsis circadian oscillator. Plant Cell. 26, 2843-2857 (2014).

[59]

Sparkes, I. A., Runions, et al. Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants. Nat. Protoc. 1, 2019-2025 (2006).

[60]

Brückner, A. et al. Yeast two-hybrid, a powerful tool for systems biology. Int. J. Mol. Sci. 10, 2763-2788 (2009).

[61]

Walter, M. et al. Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation. Plant J. 40, 428-438 (2010).

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