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Dysfunction of Telomeric Cdc13-Stn1-Ten1 Simultaneously Activates DNA Damage and Spindle Checkpoints.
- Source :
-
Cells [Cells] 2024 Sep 25; Vol. 13 (19). Date of Electronic Publication: 2024 Sep 25. - Publication Year :
- 2024
-
Abstract
- Telomeres, the ends of eukaryotic linear chromosomes, are composed of repeated DNA sequences and specialized proteins, with the conserved telomeric Cdc13/CTC1-Stn1-Ten1 (CST) complex providing chromosome stability via telomere end protection and the regulation of telomerase accessibility. In this study, SIZ1 , coding for a SUMO E3 ligase, and TOP2 (a SUMO target for Siz1 and Siz2) were isolated as extragenic suppressors of Saccharomyces cerevisiae CST temperature-sensitive mutants. ten1 - sz , stn1 - sz and cdc13 - sz mutants were isolated next due to being sensitive to intracellular Siz1 dosage. In parallel, strong negative genetic interactions between mutants of CST and septins were identified, with septins being noticeably sumoylated through the action of Siz1. The temperature-sensitive arrest in these new mutants of CST was dependent on the G2/M Mad2-mediated and Bub2-mediated spindle checkpoints as well as on the G2/M Mec1-mediated DNA damage checkpoint. Our data suggest the existence of yet unknown functions of the telomeric Cdc13-Stn1-Ten1 complex associated with mitotic spindle positioning and/or assembly that could be further elucidated by studying these new ten1 - sz , stn1 - sz and cdc13 - sz mutants.
- Subjects :
- Mutation genetics
Chromosomal Proteins, Non-Histone metabolism
Chromosomal Proteins, Non-Histone genetics
Saccharomyces cerevisiae Proteins metabolism
Saccharomyces cerevisiae Proteins genetics
DNA Damage
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae metabolism
Telomere metabolism
Telomere genetics
Telomere-Binding Proteins metabolism
Telomere-Binding Proteins genetics
Spindle Apparatus metabolism
Cell Cycle Proteins metabolism
Cell Cycle Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 13
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 39404369
- Full Text :
- https://doi.org/10.3390/cells13191605