Specific control of Arabidopsis BAK1/SERK4-regulated cell death by protein glycosylation

Nature Plants

Volumn 2, Issue , 2016, Pages

  De Oliveira, Marcos V V ^a   Xu, Guangyuan ^a   Li, Bo ^a   De Souza Vespoli, Luciano ^a,b   Meng, Xiangzong ^a   Chen, Xin ^a   Yu, Xiao ^a   De Souza, Suzane Ariádina ^a,b   Intorne, Aline C ^a,b   Manhães, Ana Marcia E De A ^a,b   Musinsky, Abbey L ^a,c   Koiwa, Hisashi ^a   De Souza Filho, Gonçalo A ^b   Shan, Libo ^a   He, Ping ^a  

^a TEXAS A AND M UNIVERSITY   (United States)

^b STATE UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^c UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS PROTEIN; BAK1 PROTEIN, ARABIDOPSIS; CRK4 PROTEIN, ARABIDOPSIS; PROTEIN KINASE; PROTEIN SERINE THREONINE KINASE; SERK4 PROTEIN, ARABIDOPSIS;

ARABIDOPSIS; CELL DEATH; CYTOLOGY; ENZYMOLOGY; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; GLYCOSYLATION; METABOLISM; MUTATION; PHENOTYPE; PHYSIOLOGY; PLANT LEAF; PLANT ROOT; SEEDLING;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CELL DEATH; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, PLANT; GLYCOSYLATION; MUTATION; PHENOTYPE; PLANT LEAVES; PLANT ROOTS; PROTEIN KINASES; PROTEIN-SERINE-THREONINE KINASES; SEEDLINGS;

EID: 84955510546     PISSN: None     EISSN: 20550278     Source Type: Journal    
DOI: 10.1038/nplants.2015.218     Document Type: Article

References (50)

1. Shiu, S. H. & Bleecker, A. B. Expansion of the receptor-like kinase/Pelle gene family and receptor-like proteins in Arabidopsis. Plant Physiol. 132, 530-543 (2003).
2. Belkhadir, Y., Yang, L., Hetzel, J., Dangl, J. L. & Chory, J. The growth-defense pivot: crisis management in plants mediated by LRR-RK surface receptors. Trends Biochem. Sci. 39, 447-456 (2014).
3. Li, J. & Chory, J. A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction. Cell 90, 929-938 (1997).
4. Gomez-Gomez, L. & Boller, T. FLS2: an LRR receptor-like kinase involved in the perception of the bacterial elicitor flagellin in Arabidopsis. Mol. Cell 5, 1003-1011 (2000).
5. Gou, X. et al. Genetic evidence for an indispensable role of somatic embryogenesis receptor kinases in brassinosteroid signaling. PLoS Genet. 8, e1002452 (2012).
6. Aan den Toorn, M., Albrecht, C. & de Vries, S. On the origin of SERKs: bioinformatics analysis of the somatic embryogenesis receptor kinases. Mol. Plant 8, 762-782 (2015).
7. Albrecht, C., Russinova, E., Hecht, V., Baaijens, E. & de Vries, S. The Arabidopsis thaliana SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASES 1 and 2 control male sporogenesis. Plant Cell 17, 3337-3349 (2005).
8. Colcombet, J., Boisson-Dernier, A., Ros-Palau, R., Vera, C. E. & Schroeder, J. I. Arabidopsis SOMATIC EMBRYOGENESIS RECEPTOR KINASES 1 and 2 are essential for tapetum development and microspore maturation. Plant Cell 17, 3350-3361 (2005).
9. Chinchilla, D. et al. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature 448, 497-U412 (2007).
10. Heese, A. et al. The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants. Proc. Natl Acad. Sci. USA 104, 12217-12222 (2007).
11. Postel, S. et al. The multifunctional leucine-rich repeat receptor kinase BAK1 is implicated in Arabidopsis development and immunity. Eur. J. Cell Biol. 89, 169-174 (2010).
12. Roux, M. et al. The Arabidopsis leucine-rich repeat receptor-like kinases BAK1/SERK3 and BKK1/SERK4 are required for innate immunity to hemibiotrophic and biotrophic pathogens. Plant Cell 23, 2440-2455 (2011).
13. Li, J. et al. BAK1, an Arabidopsis LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling. Cell 110, 213-222 (2002).
14. Nam, K. H. & Li, J. BRI1/BAK1, a receptor kinase pair mediating brassinosteroid signaling. Cell 110, 203-212 (2002).
15. Meng, X. et al. Differential function of Arabidopsis SERK family receptor-like kinases in stomatal patterning. Curr. Biol. 25, 2361-2372 (2015).
16. Wang, J. et al. Allosteric receptor activation by the plant peptide hormone phytosulfokine. Nature 525, 265-268 (2015).
17. +-ATPase, and BAK1. Plant Cell 27, 1718-1729 (2015).
18. He, K. et al. BAK1 and BKK1 regulate brassinosteroid-dependent growth and brassinosteroid-independent cell-death pathways. Curr. Biol. 17, 1109-1115 (2007).
19. Kemmerling, B. et al. The BRI1-associated kinase 1, BAK1, has a brassinolide-independent role in plant cell-death control. Curr. Biol. 17, 1116-1122 (2007).
20. Gao, M. et al. Regulation of cell death and innate immunity by two receptor-like kinases in Arabidopsis. Cell Host Microbe 6, 34-44 (2009).
21. Burch-Smith, T. M., Schiff, M., Liu, Y. & Dinesh-Kumar, S. P. Efficient virus-induced gene silencing in Arabidopsis. Plant Physiol. 142, 21-27 (2006).
22. Gao, M. H. et al. MEKK1, MKK1/MKK2 and MPK4 function together in a mitogen-activated protein kinase cascade to regulate innate immunity in plants. Cell Res. 18, 1190-1198 (2008).
23. Zhang, Q., Sun, T. & Zhang, Y. ER quality control components UGGT and STT3a are required for activation of defense responses in Bir1-1. PLoS ONE 10, e0120245 (2015).
24. Hua, J. Modulation of plant immunity by light, circadian rhythm, and temperature. Curr. Opin. Plant Biol. 16, 406-413 (2013).
25. Koiwa, H. et al. The STT3a subunit isoform of the Arabidopsis oligosaccharyltransferase controls adaptive responses to salt/osmotic stress. Plant Cell 15, 2273-2284 (2003).
26. Farid, A. et al. Specialized roles of the conserved subunit OST3/6 of the oligosaccharyltransferase complex in innate immunity and tolerance to abiotic stresses. Plant Physiol. 162, 24-38 (2013).
27. Liu, Y. & Li, J. Endoplasmic reticulum-mediated protein quality control in Arabidopsis. Front. Plant Sci. 5, 162 (2014).
28. Pattison, R. J. & Amtmann, A. N-glycan production in the endoplasmic reticulum of plants. Trends Plant Sci.14, 92-99 (2009).
29. Farid, A. et al. Arabidopsis thaliana alpha1,2-glucosyltransferase (ALG10) is required for efficient N-glycosylation and leaf growth. Plant J. 68, 314-325 (2011).
30. Hong, Z. et al. Evolutionarily conserved glycan signal to degrade aberrant brassinosteroid receptors in Arabidopsis. Proc. Natl Acad. Sci. USA 109, 11437-11442 (2012).
31. Howell, S. H. Endoplasmic reticulum stress responses in plants. Annu. Rev. Plant Biol. 64, 477-499 (2013).
32. Sun, T., Zhang, Q., Gao, M. & Zhang, Y. Regulation of SOBIR1 accumulation and activation of defense responses in bir1-1 by specific components of ER quality control. Plant J. 77, 748-756 (2014).
33. Nekrasov, V. et al. Control of the pattern-recognition receptor EFR by an ER protein complex in plant immunity. EMBO J. 28, 3428-3438 (2009).
34. Saijo, Y. et al. Receptor quality control in the endoplasmic reticulum for plant innate immunity. EMBO J. 28, 3439-3449 (2009).
35. Lu, X. et al. Uncoupling of sustained MAMP receptor signaling from early outputs in an Arabidopsis endoplasmic reticulum glucosidase II allele. Proc. Natl Acad. Sci. USA 106, 22522-22527 (2009).
36. Li, J. et al. Specific ER quality control components required for biogenesis of the plant innate immune receptor EFR. Proc. Natl Acad. Sci. USA 106, 15973-15978 (2009).
37. Haweker, H. et al. Pattern recognition receptors require N-glycosylation to mediate plant immunity. J. Biol. Chem. 285, 4629-4636 (2010).
38. von Numers, N. et al. Requirement of a homolog of glucosidase II beta-subunit for EFR-mediated defense signaling in Arabidopsis thaliana. Mol. Plant 3, 740-750 (2010).
39. Jin, H., Yan, Z., Nam, K. H. & Li, J. Allele-specific suppression of a defective brassinosteroid receptor reveals a physiological role of UGGT in ER quality control. Mol. Cell 26, 821-830 (2007).
40. Jin, H., Hong, Z., Su, W. & Li, J. M. A plant-specific calreticulin is a key retention factor for a defective brassinosteroid receptor in the endoplasmic reticulum. Proc. Natl Acad. Sci. USA 106, 13612-13617 (2009).
41. Kang, J. S. et al. Salt tolerance of Arabidopsis thaliana requires maturation of N-glycosylated proteins in the Golgi apparatus. Proc. Natl Acad. Sci. USA 105, 5933-5938 (2008).
42. Deng, Y., Srivastava, R. & Howell, S. H. Protein kinase and ribonuclease domains of IRE1 confer stress tolerance, vegetative growth, and reproductive development in Arabidopsis. Proc. Natl Acad. Sci. USA 110, 19633-19638 (2013).
43. Wu, S., Shan, L. & He, P. Microbial signature-triggered plant defense responses and early signaling mechanisms. Plant Sci. 228C, 118-126 (2014).
44. Chen, K., Fan, B., Du, L. & Chen, Z. Activation of hypersensitive cell death by pathogen-induced receptor-like protein kinases from Arabidopsis. Plant Mol. Biol. 56, 271-283 (2004).
45. Chen, K., Du, L. & Chen, Z. Sensitization of defense responses and activation of programmed cell death by a pathogen-induced receptor-like protein kinase in Arabidopsis. Plant Mol. Biol. 53, 61-74 (2003).
46. Acharya, B. R. et al. Overexpression of CRK13, an Arabidopsis cysteine-rich receptor-like kinase, results in enhanced resistance to Pseudomonas syringae. Plant J. 50, 488-499 (2007).
47. Liebrand, T. W. H., van den Burg, H. A. & Joosten, M. H. A. J. Two for all: receptor-associated kinases SOBIR1 and BAK1. Trends Plant Sci. 19, 123-132 (2014).
48. Schwessinger, B. et al. Phosphorylation-dependent differential regulation of plant growth, cell death, and innate immunity by the regulatory receptor-like kinase BAK1. PLoS Genet. 7, e1002046 (2011).
49. Yeh, Y. H., Chang, Y. H., Huang, P. Y., Huang, J. B. & Zimmerli, L. Enhanced Arabidopsis pattern-triggered immunity by overexpression of cysteine-rich receptor-like kinases. Frontiers in plant science 6, 322 (2015).
50. 2+- dependent protein kinases. PLoS Pathog. 9, 14 (2013).