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dc.contributor.authorKesten, Christopher
dc.contributor.authorGarcía-Moreno, Álvaro
dc.contributor.authorAmorim-Silva, Vitor
dc.contributor.authorMenna, Alexandra
dc.contributor.authorCastillo-Garriga, Araceli 
dc.contributor.authorPercio, Francisco
dc.contributor.authorArmengot, Laia
dc.contributor.authorRuiz-López, Noemí 
dc.contributor.authorJaillais, Yvon
dc.contributor.authorSánchez-Rodríguez, Clara
dc.contributor.authorBotella-Mesa, Miguel Ángel 
dc.date.accessioned2024-10-08T10:57:12Z
dc.date.available2024-10-08T10:57:12Z
dc.date.issued2022-11-16
dc.identifier.citationChristopher Kesten et al. ,Peripheral membrane proteins modulate stress tolerance by safeguarding cellulose synthases.Sci. Adv.8,eabq6971(2022).DOI:10.1126/sciadv.abq6971es_ES
dc.identifier.urihttps://hdl.handle.net/10630/34503
dc.description.abstractControlled primary cell wall remodeling allows plant growth under stressful conditions, but how these changes are conveyed to adjust cellulose synthesis is not understood. Here, we identify the TETRATRICOPEPTIDE THIOREDOXIN-LIKE (TTL) proteins as new members of the cellulose synthase complex (CSC) and describe their unique and hitherto unknown dynamic association with the CSC under cellulose-deficient conditions. We find that TTLs are essential for maintaining cellulose synthesis under high-salinity conditions, establishing a stress-resilient cortical microtubule array, and stabilizing CSCs at the plasma membrane. To fulfill these functions, TTLs interact with CELLULOSE SYNTHASE 1 (CESA1) and engage with cortical microtubules to promote their polymerization. We propose that TTLs function as bridges connecting stress perception with dynamic regulation of cellulose biosynthesis at the plasma membrane.es_ES
dc.description.sponsorshipThis work was funded by the Spanish Ministry for Science and Innovation (MCIN/AEI/ 10.13039/501100011033 1-PID2020-114419RB-I00, PGC2018-098789-B-I00, and PID2019-107657RB-C22 to M.A.B., N.R.-L., and A.G.C., respectively), the Andalusian Research Plan cofinanced by the European Union (PAIDI 2020-PY20_00084 and UMA20-FEDERJA-023) to M.A.B. and Junta de Andalucía UMA-FEDER project (UMA18-FEDERJA-154) to N.R.-L., and the Swiss National foundation to C.S.-R. (SNF 31003A_163065/1 to AM). C.K. was supported by a Peter und Traudl Engelhorn-Stiftung fellowship, an ETH Career Seed Grant (SEED-05 19-2) of the ETH Foundation, an Emerging Investigator grant (NNF20OC0060564) of the Novo Nordisk Foundation, and an Experiment grant (R346-2020-1546) of the Lundbeck foundation. Á.G.-M. was supported by BES-2015-071256 and EMBO Short-Term 7632 Fellowships. F.P. was supported by and FPU19/02219 fellowship. V.A.-S. was supported by an Emerging Investigator research project (UMA20-FEDERJA-007) and cofinanced by the “Programa Operativo FEDER 2014-2020” and by the “Consejería de Economía y Conocimiento de la Junta de Andalucía”. Y.J. was funded by the Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (grant agreement no. 101001097).es_ES
dc.language.isoenges_ES
dc.publisherAmerican Association for the Advancement of Sciencees_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectCelulosa-Síntesises_ES
dc.subject.otherCellulose synthase complexeses_ES
dc.subject.otherTetratricopeptide thioredoxin-like (TTL) proteinses_ES
dc.titlePeripheral membrane proteins modulate stress tolerance by safeguarding cellulose synthaseses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1126/sciadv.abq6971
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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