Academic Journal

Targeted degradation of abscisic acid receptors is mediated by the ubiquitin ligase substrate adaptor DDA1 in Arabidopsis

التفاصيل البيبلوغرافية
العنوان: Targeted degradation of abscisic acid receptors is mediated by the ubiquitin ligase substrate adaptor DDA1 in Arabidopsis
المؤلفون: Irigoyen, María Luisa, Iniesto, Elisa, Rodríguez Solovey, Leisa Natacha, Puga, Maria Isabel, Yanagawa, Yuki, Pick, Elah, Strickland, Elizabeth, Paz-Ares, Javier, Wei, Ning, De Jaeger, Geert, Rodríguez Egea, Pedro Luís, Deng, Xing Wang, Rubio, Vicente
المساهمون: Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes, Ministerio de Economía y Competitividad, National Science Foundation, EEUU, National Institutes of Health, EEUU
بيانات النشر: American Society of Plant Biologists
سنة النشر: 2014
المجموعة: Universitat Politécnica de Valencia: RiuNet / Politechnical University of Valencia
مصطلحات موضوعية: Tandem affinity purification, Finger E3 ligase, ABA signal-transduction, Transcription factor, Negative regulator, Positive regulator, Plant transformation, Seed germination, Stress responses, Cop9 signalosome, BIOQUIMICA Y BIOLOGIA MOLECULAR
الوصف: [EN] CULLIN4-RING E3 ubiquitin ligases (CRL4s) regulate key developmental and stress responses in eukaryotes. Studies in both animals and plants have led to the identification of many CRL4 targets as well as specific regulatory mechanisms that modulate their function. The latter involve COP10-DET1-DDB1 (CDD)-related complexes, which have been proposed to facilitate target recognition by CRL4, although the molecular basis for this activity remains largely unknown. Here, we provide evidence that Arabidopsis thaliana DET1-, DDB1-ASSOCIATED1 (DDA1), as part of the CDD complex, provides substrate specificity for CRL4 by interacting with ubiquitination targets. Thus, we show that DDA1 binds to the abscisic acid (ABA) receptor PYL8, as well as PYL4 and PYL9, in vivo and facilitates its proteasomal degradation. Accordingly, we found that DDA1 negatively regulates ABA-mediated developmental responses, including inhibition of seed germination, seedling establishment, and root growth. All other CDD components displayed a similar regulatory function, although they did not directly interact with PYL8. Interestingly, DDA1-mediated destabilization of PYL8 is counteracted by ABA, which protects PYL8 by limiting its polyubiquitination. Altogether, our data establish a function for DDA1 as a substrate receptor for CRL4-CDD complexes and uncover a mechanism for the desensitization of ABA signaling based on the regulation of ABA receptor stability. ; This research was supported by the Spanish Ministry of Economy and Competitiveness (MINECO; National Research Program, Grants BIO2010-18820 to V. R., BIO2011-29085 to J.P.-A., and BIO2011-23446 to P.L.R.; INNPACTO Program, Grant IPT-310000-2010-9 to J.P.-A.; and CONSOLIDER Program, Grant 2007-28317 to J.P.-A.), the National Science Foundation (Grant GM-47850 to X. W. D.), and the National Institutes of Health (Grant GM-47850 to X. W. D.). E. I. and L. R. were recipients of Formacion de Personal Investigador fellowships from MINECO. ; Irigoyen, ML.; Iniesto, E.; Rodríguez Solovey, LN.; ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1040-4651
1532-298X
Relation: MINECO/info:eu-repo/grantAgreement/MICINN//BIO2010-18820/ES/REGULACION DE LA MAQUINARIA DE UBIQUITINACION EN EL CONTROL DEL DESARROLLO Y DE LA RESPUESTA A ESTRES EN PLANTAS/; Plant Cell; info:eu-repo/grantAgreement/MICINN//BIO2011-29085/ES/SEÑALIZACION DEL AYUNO DE FOSFATO EN PLANTAS. VARIACION NATURAL DEL TRANSCRIPTOMA Y MECANISMOS DE CONTROL DEL REGULADOR MAESTRO PHR1/; info:eu-repo/grantAgreement/MICINN//BIO2011-23446/ES/SEÑALIZACION DE ABA MEDIADA POR LOS RECEPTORES PYR%2FPYL Y SU CONEXION CON LOS MECANISMOS DE RESISTENCIA A SEQUIA/; info:eu-repo/grantAgreement/MINECO//IPT-310000-2010-9/; info:eu-repo/grantAgreement/MINECO//2007-28317/; info:eu-repo/grantAgreement/NSF//GM-47850/; info:eu-repo/grantAgreement/NIH//GM-47850/; http://doi.org/10.1105/tpc.113.122234; urn:issn:1040-4651; http://hdl.handle.net/10251/82480; urn:eissn:1532-298X
DOI: 10.1105/tpc.113.122234
الاتاحة: http://hdl.handle.net/10251/82480
https://doi.org/10.1105/tpc.113.122234
Rights: http://rightsstatements.org/vocab/InC/1.0/ ; info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.6B3A041B
قاعدة البيانات: BASE
الوصف
تدمد:10404651
1532298X
DOI:10.1105/tpc.113.122234