ArticlePloS one2010
Diversification and Specialization of Plant RBR Ubiquitin Ligases.
Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed, 34 citations in OpenAlex.
- Construction of a Yeast Two-Hybrid Library for Lilium × formolongi and Screening for Proteins Interacting with LfSVP.Molecular biotechnology · 2026Article
- Genome-wide identification and expression analysis of RBR-type ubiquitin ligase family genes reveal the role of ZmIBR10 in maize disease resistance.BMC plant biology · 2026Article
- Genome-Wide Analysis of HECT E3 Ligases Members inInternational journal of molecular sciences · 2024Article
- Genome-Wide Identification and Analysis of Ariadne Gene Family Reveal Its Genetic Effects on Agronomic Traits ofInternational journal of molecular sciences · 2022Article
- Core Components of Abscisic Acid Signaling and Their Post-translational Modification.Frontiers in plant science · 2022Review
- Current perspectives of ubiquitination and SUMOylation in abiotic stress tolerance in plants.Frontiers in plant science · 2022Review
- Ubiquitylation of ABA Receptors and Protein Phosphatase 2C Coreceptors to Modulate ABA Signaling and Stress Response.International journal of molecular sciences · 2021Review
- Editorial: Structure, Function, and Evolution of E3 Ligases and Targets.Frontiers in plant science · 2021Article
- Exploring the Roles of HERC2 and the NEDD4L HECT E3 Ubiquitin Ligase Subfamily in p53 Signaling and the DNA Damage Response.Frontiers in oncology · 2021Review
- RBR-Type E3 Ligases and the Ubiquitin-Conjugating Enzyme UBC26 Regulate Abscisic Acid Receptor Levels and Signaling.Plant physiology · 2020Article
- Regulation of germ cell development by ARI1 family ubiquitin ligases in C. elegans.Scientific reports · 2018Article
- Origin and evolution of fungal HECT ubiquitin ligases.Scientific reports · 2018Article
- UV-B induction of the E3 ligase ARIADNE12 depends on CONSTITUTIVELY PHOTOMORPHOGENIC 1.Plant physiology and biochemistry : PPB · 2015Article
- The eukaryotic ancestor had a complex ubiquitin signaling system of archaeal origin.Molecular biology and evolution · 2015Article
- Article
- The ubiquilin gene family: evolutionary patterns and functional insights.BMC evolutionary biology · 2014Article
- Genome-wide identification and characterization of RBR ubiquitin ligase genes in soybean.PloS one · 2014Article
- Overexpression of a soybean ariadne-like ubiquitin ligase gene GmARI1 enhances aluminum tolerance in Arabidopsis.PloS one · 2014Article
- The ubiquitination machinery of the ubiquitin system.The arabidopsis book · 2014Article
- Evolution of plant HECT ubiquitin ligases.PloS one · 2013Article
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundRBR ubiquitin ligases are components of the ubiquitin-proteasome system present in all eukaryotes. They are characterized by having the RBR (RING - IBR - RING) supradomain. In this study, the patterns of emergence of RBR genes in plants are described. METHODOLOGY/PRINCIPAL
findingsPhylogenetic and structural data confirm that just four RBR subfamilies (Ariadne, ARA54, Plant I/Helicase and Plant II) exist in viridiplantae. All of them originated before the split that separated green algae from the rest of plants. Multiple genes of two of these subfamilies (Ariadne and Plant II) appeared in early plant evolution. It is deduced that the common ancestor of all plants contained at least five RBR genes and the available data suggest that this number has been increasing slowly along streptophyta evolution, although losses, especially of Helicase RBR genes, have also occurred in several lineages. Some higher plants (e. g. Arabidopsis thaliana, Oryza sativa) contain a very large number of RBR genes and many of them were recently generated by tandem duplications. Microarray data indicate that most of these new genes have low-level and sometimes specific expression patterns. On the contrary, and as occurs in animals, a small set of older genes are broadly expressed at higher levels. CONCLUSIONS/SIGNIFICANCE: The available data suggests that the dynamics of appearance and conservation of RBR genes is quite different in plants from what has been described in animals. In animals, an abrupt emergence of many structurally diverse RBR subfamilies in early animal history, followed by losses of multiple genes in particular lineages, occurred. These patterns are not observed in plants. It is also shown that while both plants and animals contain a small, similar set of essential RBR genes, the rest evolves differently. The functional implications of these results are discussed.
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