The exocyst subunit Exo70B1 is involved in the immune response of Arabidopsis thaliana to different pathogens and cell death

Plant Signaling and Behavior

Volumn 8, Issue 12, 2014, Pages

  Stegmann, Martin ^a,c   Anderson, Ryan G ^b   Westphal, Lore ^a   Rosahl, Sabine ^a   McDowell, John M ^b   Trujillo, Marco ^a  

^a LEIBNIZ INSTITUTE OF PLANT BIOCHEMISTRY   (Germany)

^b VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY   (United States)

^c SAINSBURY LABORATORY   (United Kingdom)

Author keywords

Basal resistance; Biotroph; Cell death; Hemibiotroph; Lesion mimic; Nonhost resistance; Vesicle trafficking

Indexed keywords

ARABIDOPSIS PROTEIN; EXO70B1 PROTEIN, ARABIDOPSIS; PROTEIN SUBUNIT; VESICULAR TRANSPORT PROTEIN;

ARABIDOPSIS; CELL DEATH; CYTOLOGY; GENETICS; IMMUNOLOGY; METABOLISM; MICROBIOLOGY; MUTATION; PHENOTYPE; PLANT IMMUNITY; PROTEIN SUBUNIT;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CELL DEATH; MUTATION; PHENOTYPE; PLANT IMMUNITY; PROTEIN SUBUNITS; VESICULAR TRANSPORT PROTEINS;

EID: 84892598345     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.27421     Document Type: Article

References (34)

1. Bednarek P, Kwon C, Schulze-Lefert P. Not a peripheral issue: secretion in plant-microbe interactions. Curr Opin Plant Biol 2010; 13:378-87; PMID:20558098; http://dx.doi.org/10.1016/j. pbi.2010.05.002
2. Collins NC, Thordal-Christensen H, Lipka V, Bau S, Kombrink E, Qiu JL, Hückelhoven R, Stein M, Freialdenhoven A, Somerville SC, et al. SNAREprotein-mediated disease resistance at the plant cell wall. Nature 2003; 425:973-7; PMID:14586469; http://dx.doi.org/10.1038/nature02076
3. Ali GS, Prasad KV, Day I, Reddy AS. Liganddependent reduction in the membrane mobility of FLAGELLIN SENSITIVE2, an arabidopsis receptor-like kinase. Plant Cell Physiol 2007; 48:1601-11; PMID:17925310; http://dx.doi.org/10.1093/pcp/ pcm132
4. Kwon C, Neu C, Pajonk S, Yun HS, Lipka U, Humphry M, Bau S, Straus M, Kwaaitaal M, Rampelt H, et al. Co-option of a default secretory pathway for plant immune responses. Nature 2008; 451:835-40; PMID:18273019; http://dx.doi. org/10.1038/nature06545
5. Hoef le C, Huesmann C, Schultheiss H, Börnke F, Hensel G, Kumlehn J, Hückelhoven R. A barley ROP GTPase ACTIVATING PROTEIN associates with microtubules and regulates entry of the barley powdery mildew fungus into leaf epidermal cells. Plant Cell 2011; 23:2422-39; PMID:21685259; http://dx.doi.org/10.1105/tpc.110.082131
6. Opalski KS, Schultheiss H, Kogel KH, Hückelhoven R. The receptor-like MLO protein and the RAC/ ROP family G-protein RACB modulate actin reorganization in barley attacked by the biotrophic powdery mildew fungus Blumeria graminis f. sp. hordei. Plant J 2005; 41:291-303; PMID:15634205; http:// dx.doi.org/10.1111/j.1365-313X.2004.02292.x
7. Robatzek S, Chinchilla D, Boller T. Ligand-induced endocytosis of the pattern recognition receptor FLS2 in Arabidopsis. Genes Dev 2006; 20:537-42; PMID:16510871; http://dx.doi.org/10.1101/ gad.366506
8. Chinchilla D, Bauer Z, Regenass M, Boller T, Felix G. The Arabidopsis receptor kinase FLS2 binds f lg22 and determines the specificity of f lagellin perception. Plant Cell 2006; 18:465-76; PMID:16377758; http://dx.doi.org/10.1105/tpc.105.036574
9. Lu D, Lin W, Gao X, Wu S, Cheng C, Avila J, Heese A, Devarenne TP, He P, Shan L. Direct ubiquitination of pattern recognition receptor FLS2 attenuates plant innate immunity. Science 2011; 332:1439-42; PMID:21680842; http://dx.doi.org/10.1126/ science.1204903
10. Smith JM, Salamango DJ, Leslie ME, Collins CA, Heese A. Sensitivity to flg22 is modulated by ligandinduced degradation and de novo synthesis of the endogenous flagellin-receptor FLS2. Plant Physiol 2013; PMID:24220680; http://dx.doi.org/10.1104/ pp.113.229179
11. Göhre V, Spallek T, Häweker H, Mersmann S, Mentzel T, Boller T, de Torres M, Mansfield JW, Robatzek S. Plant pattern-recognition receptor FLS2 is directed for degradation by the bacterial ubiquitin ligase AvrPtoB. Curr Biol 2008; 18:1824-32; PMID:19062288; http://dx.doi.org/10.1016/j. cub.2008.10.063
12. Beck M, Zhou J, Faulkner C, MacLean D, Robatzek S. Spatio-temporal cellular dynamics of the Arabidopsis f lagellin receptor reveal activation status-dependent endosomal sorting. Plant Cell 2012; 24:4205-19; PMID:23085733; http://dx.doi. org/10.1105/tpc.112.100263
13. Furlan G, Klinkenberg J, Trujillo M. Regulation of plant immune receptors by ubiquitination. Front Plant Sci 2012; 3:238; PMID:23109936; http:// dx.doi.org/10.3389/fpls.2012.00238
14. MacGurn JA, Hsu PC, Emr SD. Ubiquitin and membrane protein turnover: from cradle to grave. Annu Rev Biochem 2012; 81:231-59; PMID:22404628; http://dx.doi.org/10.1146/ annurev-biochem-060210-093619
15. Trujillo M, Ichimura K, Casais C, Shirasu K. Negative regulation of PAMP-triggered immunity by an E3 ubiquitin ligase triplet in Arabidopsis. Curr Biol 2008; 18:1396-401; PMID:18771922; http:// dx.doi.org/10.1016/j.cub.2008.07.085
16. Stegmann M, Anderson RG, Ichimura K, Pecenkova T, Reuter P, Žársky V, McDowell JM, Shirasu K, Trujillo M. The ubiquitin ligase PUB22 targets a subunit of the exocyst complex required for PAMPtriggered responses in Arabidopsis. Plant Cell 2012; 24:4703-16; PMID:23170036; http://dx.doi. org/10.1105/tpc.112.104463
17. Pecenková T, Hála M, Kulich I, Kocourková D, Drdová E, Fendrych M, Toupalová H, Zársky V. The role for the exocyst complex subunits Exo70B2 and Exo70H1 in the plant-pathogen interaction. J Exp Bot 2011; 62:2107-16; PMID:21199889; http://dx.doi.org/10.1093/jxb/erq402
18. Ostertag M, Stammler J, Douchkov D, Eichmann R, Hückelhoven R. The conserved oligomeric Golgi complex is involved in penetration resistance of barley to the barley powdery mildew fungus. Mol Plant Pathol 2013; 14:230-40; PMID:23145810; http:// dx.doi.org/10.1111/j.1364-3703.2012.00846.x
19. Kulich I, Pečenková T, Sekereš J, Smetana O, Fendrych M, Foissner I, Höftberger M, Zárský V. Arabidopsis exocyst subcomplex containing subunit EXO70B1 is involved in autophagy-related transport to the vacuole. Traffic 2013; 14:1155-65; PMID:23944713
20. Heider MR, Munson M. Exorcising the exocyst complex. Traffic 2012; 13:898-907; PMID:22420621; http://dx.doi. org/10.1111/j.1600-0854.2012.01353.x
21. Samuel MA, Chong YT, Haasen KE, Aldea-Brydges MG, Stone SL, Goring DR. Cellular pathways regulating responses to compatible and self-incompatible pollen in Brassica and Arabidopsis stigmas intersect at Exo70A1, a putative component of the exocyst complex. Plant Cell 2009; 21:2655-71; PMID:19789280; http://dx.doi.org/10.1105/ tpc.109.069740
22. Zárský V, Cvrcková F, Potocký M, Hála M. Exocytosis and cell polarity in plants-exocyst and recycling domains. New Phytol 2009; 183:255-72; PMID:19496948; http://dx.doi. org/10.1111/j.1469-8137.2009.02880.x
23. He B, Xi F, Zhang X, Zhang J, Guo W. Exo70 interacts with phospholipids and mediates the targeting of the exocyst to the plasma membrane. EMBO J 2007; 26:4053-65; PMID:17717527; http://dx.doi. org/10.1038/sj.emboj.7601834
24. Cvrčková F, Grunt M, Bezvoda R, Hála M, Kulich I, Rawat A, Zárský V. Evolution of the land plant exocyst complexes. Front Plant Sci 2012; 3:159; PMID:22826714; http://dx.doi.org/10.3389/ fpls.2012.00159
25. Brooks DM, Hernández-Guzmán G, Kloek AP, Alarcón-Chaidez F, Sreedharan A, Rangaswamy V, Peñaloza-Vázquez A, Bender CL, Kunkel BN. Identification and characterization of a welldefined series of coronatine biosynthetic mutants of Pseudomonas syringae pv. tomato DC3000. Mol Plant Microbe Interact 2004; 17:162-74; PMID:14964530; http://dx.doi.org/10.1094/ MPMI.2004.17.2.162
26. Kopischke M, Westphal L, Schneeberger K, Clark R, Ossowski S, Wewer V, Fuchs R, Landtag J, Hause G, Dörmann P, et al. Impaired sterol ester synthesis alters the response of Arabidopsis thaliana to Phytophthora infestans. Plant J 2013; 73:456-68; PMID:23072470; http://dx.doi.org/10.1111/ tpj.12046
27. Trujillo M, Kogel K-H, Hückelhoven R. Superoxide and hydrogen peroxide play different roles in the nonhost interaction of barley and wheat with inappropriate formae speciales of Blumeria graminis. Mol Plant Microbe Interact 2004; 17:304-12; PMID:15000397; http://dx.doi.org/10.1094/ MPMI.2004.17.3.304
28. Jacobs AK, Lipka V, Burton RA, Panstruga R, Strizhov N, Schulze-Lefert P, Fincher GB. An Arabidopsis Callose Synthase, GSL5, Is Required for Wound and Papillary Callose Formation. Plant Cell 2003; 15:2503-13; PMID:14555698; http://dx.doi. org/10.1105/tpc.016097
29. Nishimura MT, Stein M, Hou BH, Vogel JP, Edwards H, Somerville SC. Loss of a callose synthase results in salicylic acid-dependent disease resistance. Science 2003; 301:969-72; PMID:12920300; http://dx.doi.org/10.1126/science.1086716
30. Bednarek P, Pislewska-Bednarek M, Svatos A, Schneider B, Doubsky J, Mansurova M, Humphry M, Consonni C, Panstruga R, Sanchez-Vallet A, et al. A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense. Science 2009; 323:101-6; PMID:19095900; http:// dx.doi.org/10.1126/science.1163732
31. Lipka V, Dittgen J, Bednarek P, Bhat R, Wiermer M, Stein M, Landtag J, Brandt W, Rosahl S, Scheel D, et al. Pre-and postinvasion defenses both contribute to nonhost resistance in Arabidopsis. Science 2005; 310:1180-3; PMID:16293760; http://dx.doi. org/10.1126/science.1119409
32. Hofius D, Schultz-Larsen T, Joensen J, Tsitsigiannis DI, Petersen NH, Mattsson O, Jørgensen LB, Jones JD, Mundy J, Petersen M. Autophagic components contribute to hypersensitive cell death in Arabidopsis. Cell 2009; 137:773-83; PMID:19450522; http:// dx.doi.org/10.1016/j.cell.2009.02.036
33. Yoshimoto K, Jikumaru Y, Kamiya Y, Kusano M, Consonni C, Panstruga R, Ohsumi Y, Shirasu K. Autophagy negatively regulates cell death by controlling NPR1-dependent salicylic acid signaling during senescence and the innate immune response in Arabidopsis. Plant Cell 2009; 21:2914-27; PMID:19773385; http://dx.doi.org/10.1105/ tpc.109.068635
34. Hofius D, Munch D, Bressendorff S, Mundy J, Petersen M. Role of autophagy in disease resistance and hypersensitive response-associated cell death. Cell Death Differ 2011; 18:1257-62; PMID:21527936; http://dx.doi.org/10.1038/ cdd.2011.43