WeightNameValue
1000 Titel
  • Rate Motifs Tune Auxin/Indole-3-Acetic Acid Degradation Dynamics
1000 Autor/in
  1. Moss, Britney L |
  2. Mao, Haibin |
  3. Guseman, Jessica M |
  4. Hinds, Thomas R |
  5. Hellmuth, Antje |
  6. Kovenock, Marlies |
  7. Noorassa, Anisa |
  8. Lanctot, Amy |
  9. Zheng, Ning |
  10. Nemhauser, Jennifer L |
  11. Calderón Villalobos, Luz Irina A. |
1000 Erscheinungsjahr 2015
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2015-09-04
1000 Erschienen in
1000 Quellenangabe
  • 169(1): 803-813
1000 FRL-Sammlung
1000 Verlagsversion
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577399/ |
  • https://doi.org/10.1104/pp.15.00587 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Ubiquitin-mediated protein degradation is a common feature in diverse plant cell signaling pathways; however, the factors that control the dynamics of regulated protein turnover are largely unknown. One of the best-characterized families of E3 ubiquitin ligases facilitates ubiquitination of auxin (aux)/indole-3-acetic acid (IAA) repressor proteins in the presence of auxin. Rates of auxin-induced degradation vary widely within the Aux/IAA family, and sequences outside of the characterized degron (the minimum region required for auxin-induced degradation) can accelerate or decelerate degradation. We have used synthetic auxin degradation assays in yeast (Saccharomyces cerevisiae) and in plants to characterize motifs flanking the degron that contribute to tuning the dynamics of Aux/IAA degradation. The presence of these rate motifs is conserved in phylogenetically distant members of the Arabidopsis (Arabidopsis thaliana) Aux/IAA family, as well as in their putative Brassica rapa orthologs. We found that rate motifs can act by enhancing interaction between repressors and the E3, but that this is not the only mechanism of action. Phenotypes of transgenic plants expressing a deletion in a rate motif in IAA28 resembled plants expressing degron mutations, underscoring the functional relevance of Aux/IAA degradation dynamics in regulating auxin responses.
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/TW9zcywgQnJpdG5leSBM|https://frl.publisso.de/adhoc/creator/TWFvLCBIYWliaW4=|https://frl.publisso.de/adhoc/creator/R3VzZW1hbiwgSmVzc2ljYSBN|https://frl.publisso.de/adhoc/creator/SGluZHMsIFRob21hcyBS|https://frl.publisso.de/adhoc/creator/SGVsbG11dGgsIEFudGpl|https://frl.publisso.de/adhoc/creator/S292ZW5vY2ssIE1hcmxpZXM=|https://frl.publisso.de/adhoc/creator/Tm9vcmFzc2EsIEFuaXNh|https://frl.publisso.de/adhoc/creator/TGFuY3RvdCwgQW15|https://frl.publisso.de/adhoc/creator/WmhlbmcsIE5pbmc=|https://frl.publisso.de/adhoc/creator/TmVtaGF1c2VyLCBKZW5uaWZlciBM|http://orcid.org/0000-0002-6093-1478
1000 Label
1000 Förderer
  1. Paul G. Allen Family Foundation |
  2. National Science Foundation |
  3. National Institutes of Health (NIH) |
1000 Fördernummer
  1. -
  2. MCB–1411949; DBI–0115870
  3. R01–GM107084; R01–CA076584; F32CA180514
1000 Förderprogramm
  1. -
  2. -
  3. -
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Paul G. Allen Family Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer National Science Foundation |
    1000 Förderprogramm -
    1000 Fördernummer MCB–1411949; DBI–0115870
  3. 1000 joinedFunding-child
    1000 Förderer National Institutes of Health (NIH) |
    1000 Förderprogramm -
    1000 Fördernummer R01–GM107084; R01–CA076584; F32CA180514
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6406574.rdf
1000 Erstellt am 2018-01-30T19:04:51.648+0100
1000 Erstellt von 218
1000 beschreibt frl:6406574
1000 Bearbeitet von 288
1000 Zuletzt bearbeitet 2021-03-31T07:51:59.650+0200
1000 Objekt bearb. Wed Mar 31 07:51:59 CEST 2021
1000 Vgl. frl:6406574
1000 Oai Id
  1. oai:frl.publisso.de:frl:6406574 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

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