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Characterization of the Arabidopsis thaliana E3 Ubiquitin-Ligase AtSINAL7 and identification of the Ubiquitination sites
- Source :
- CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET, PLoS ONE, PLoS ONE, Public Library of Science, 2013, 8 (8), pp.1-8. ⟨10.1371/journal.pone.0073104⟩, Plos One 8 (8), 1-8. (2013), PLoS ONE, Vol 8, Iss 8, p e73104 (2013)
- Publication Year :
- 2013
- Publisher :
- Public Library Science, 2013.
-
Abstract
- Protein ubiquitination leading to degradation by the proteasome is an important mechanism in regulating key cellular functions. Protein ubiquitination is carried out by a three step process involving ubiquitin (Ub) activation by a E1 enzyme, the transfer of Ub to a protein E2, finally an ubiquitin ligase E3 catalyzes the transfer of the Ub peptide to an acceptor protein. The E3 component is responsible for the specific recognition of the target, making the unveiling of E3 components essential to understand the mechanisms regulating fundamental cell processes through the protein degradation pathways. The Arabidopsis thaliana seven in absentia-like 7 (AtSINAL7) gene encodes for a protein with characteristics from a C3HC4-type E3 ubiquitin ligase. We demonstrate here that AtSINAL7 protein is indeed an E3 protein ligase based on the self-ubiquitination in vitro assay. This activity is dependent of the presence of a Lys residue in position 124. We also found that higher AtSINAL7 transcript levels are present in tissues undergoing active cell division during floral development. An interesting observation is the circadian expression pattern of AtSINAL7 mRNA in floral buds. Furthermore, UV–B irradiation induces the expression of this transcript indicating that AtSINAL7 may be involved in a wide range of different cell processes. Fil: Peralta, Diego Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Centro de Estudios Fotosinteticos y Bioquimicos. Universidad Nacional de Rosario. Facultad de Cs.bioquímicas y Farmaceuticas. Centro de Estudios Fotosinteticos y Bioquimicos; Argentina Fil: Araya, Alejandro. Centre National de la Recherche Scientifique; Francia. Institut National de la Recherche Agronomique; Francia Fil: Nardi, Cristina Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús). Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas "Dr. Raúl Alfonsín" (sede Chascomús); Argentina Fil: Busi, María Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Centro de Estudios Fotosinteticos y Bioquimicos. Universidad Nacional de Rosario. Facultad de Cs.bioquímicas y Farmaceuticas. Centro de Estudios Fotosinteticos y Bioquimicos; Argentina Fil: Gomez Casati, Diego Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Centro de Estudios Fotosinteticos y Bioquimicos. Universidad Nacional de Rosario. Facultad de Cs.bioquímicas y Farmaceuticas. Centro de Estudios Fotosinteticos y Bioquimicos; Argentina
- Subjects :
- 0106 biological sciences
e3 ubiquitine ligase
Seven in absentia
développement végétal
Arabidopsis
lcsh:Medicine
Ubiquitin-conjugating enzyme
01 natural sciences
purl.org/becyt/ford/1 [https]
Ubiquitin
Gene Expression Regulation, Plant
lcsh:Science
2. Zero hunger
chemistry.chemical_classification
0303 health sciences
Multidisciplinary
Vegetal Biology
biology
Bioquímica y Biología Molecular
AtSINAL7
Ubiquitin ligase
Cell biology
CIENCIAS NATURALES Y EXACTAS
Research Article
Ultraviolet Rays
Ubiquitin-Protein Ligases
Protein degradation
Gene Expression Regulation, Enzymologic
Ciencias Biológicas
03 medical and health sciences
DDB1
physiologie végétale
[SDV.BV]Life Sciences [q-bio]/Vegetal Biology
purl.org/becyt/ford/1.6 [https]
activité cellulaire
030304 developmental biology
DNA ligase
Arabidopsis Proteins
lcsh:R
arabidopsis thaliana
Ubiquitination
Molecular biology
Protein ubiquitination
cycle cellulaire
proteasome
chemistry
Proteasome
biology.protein
lcsh:Q
Biologie végétale
010606 plant biology & botany
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Database :
- OpenAIRE
- Journal :
- CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET, PLoS ONE, PLoS ONE, Public Library of Science, 2013, 8 (8), pp.1-8. ⟨10.1371/journal.pone.0073104⟩, Plos One 8 (8), 1-8. (2013), PLoS ONE, Vol 8, Iss 8, p e73104 (2013)
- Accession number :
- edsair.doi.dedup.....7e065890e2411bce2fe83065b55ebd23
- Full Text :
- https://doi.org/10.1371/journal.pone.0073104