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Investigating the Function of Coronin A in the Early Starvation Response of Dictyostelium discoideum by Aggregation Assays
Published on: June 18, 2016
The COP9 signalosome regulates cell proliferation of Dictyostelium discoideum
1Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-8028, USA.
Abstract:
Regulated protein destruction involving SCF (Skp1/Cullin/F-box, E3 ubiquitin ligase) complexes is required for multicellular development of Dictyostelium discoideum. Dynamic modification of cullin by nedd8 is required for the proper action of SCF. The COP9 signalosome (CSN), first identified in a signaling pathway for light response in plants, functions as a large multi-protein complex that regulates cullin neddylation in eukaryotes. Still, there is extreme sequence divergence of CSN subunits of the yeasts in comparison to the multicellular plants and animals. Using the yeast two-hybrid system, we have identified the CSN5 subunit as a potential interacting partner of a cell surface receptor of Dictyostelium. We further identified and characterized all 8 CSN subunits in Dictyostelium discoideum. Remarkably, despite the ancient origin of Dictyostelium, its CSN proteins cluster very closely with their plant and animal counterparts. We additionally show that the Dictyostelium subunits, like those of other systems are capable of multi-protein interactions within the CSN complex. Our data also indicate that CSN5 (and CSN2) are essential for cell proliferation in Dictyostelium, a phenotype similar to that of multicellular organisms, but distinct from that of the yeasts. Finally, we speculate on a potential role of CSN in cullin function and regulated protein destruction during multicellular development of Dictyostelium.
Insights
The COP9 signalosome (CSN) complex is crucial for Dictyostelium development, with its subunits closely resembling those in plants and animals. CSN5 and CSN2 are essential for cell proliferation in this organism.
Area of Science:
- Cell Biology
- Molecular Biology
- Developmental Biology
Background:
- Regulated protein destruction via SCF (Skp1/Cullin/F-box, E3 ubiquitin ligase) complexes is vital for Dictyostelium discoideum multicellular development.
- The COP9 signalosome (CSN) regulates cullin neddylation, a key process for SCF complex function, across eukaryotes.
- CSN subunit sequences show significant divergence in yeasts compared to plants and animals.
Purpose of the Study:
- To identify and characterize the COP9 signalosome (CSN) subunits in Dictyostelium discoideum.
- To investigate the evolutionary conservation and functional roles of CSN in Dictyostelium.
- To explore the potential involvement of CSN in Dictyostelium multicellular development.
Main Methods:
- Yeast two-hybrid system to identify interacting partners.
- Identification and characterization of all 8 CSN subunits in Dictyostelium.
- Analysis of protein-protein interactions within the CSN complex.
Main Results:
- CSN5 was identified as a potential interacting partner of a Dictyostelium cell surface receptor.
- All 8 CSN subunits were identified, showing close clustering with plant and animal counterparts despite Dictyostelium's ancient origin.
- Dictyostelium CSN subunits form multi-protein interactions, and CSN5 and CSN2 are essential for cell proliferation.
Conclusions:
- Dictyostelium CSN subunits are highly conserved with those of plants and animals, suggesting ancient functional importance.
- CSN plays a critical role in Dictyostelium cell proliferation, mirroring functions in multicellular organisms.
- The study speculates a role for CSN in regulating cullin function and protein destruction during Dictyostelium multicellular development.
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