The stn1-sz2 Mutant Provides New Insight into the Impacts of Telomeric Cdc13-Stn1-Ten1 Dysfunction on Cell Cycle Progression

The conserved and essential Cdc13/CTC1-Stn1-Ten1 telomeric complex (CST) ensures chromosome stability by protecting telomere ends and regulating telomerase accessibility. In a recent study, we uncovered mutants of the <i>S</i>. <i>cerevisiae</i> CST, in which damage was sensed by the two major G2/M spindle checkpoints (one is Bub2-dependent and the other one Mad2-dependent), as well as the major G2/M DNA damage checkpoint (Mec1-dependent). In this study, we found, by fluorescence microscopy, that the stability of the mitotic tubulin spindle was profoundly affected in the best-studied of these mutants, <i>stn1</i>-<i>sz2</i>. Additional data from genetic analyses suggested the potential involvement of Stu1 and Stu2, as well as Slk19, in these defects. Throughout this study, we compared the phenotypes of <i>stn1</i>-<i>sz2</i> with those of <i>cdc13</i>-<i>1</i>, the best-studied CST mutant, which also serves as a prototype of telomere-damage-characterized CST mutants. We propose that <i>stn1</i>-<i>sz2</i> represents the prototype of <i>cst</i> mutants characterized by tubulin spindle damage. These newly described phenotypes potentially represent the basis for identifying new functions of the CST telomeric complex. These functions might consist of ensuring correct chromosome segregation through the stabilization of the mitotic spindle.

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Journal
Cells
Published
2025-05-26
DOI
https://doi.org/10.3390/cells14110784
Primary Topic
DNA Repair Mechanisms
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article
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article

The stn1-sz2 Mutant Provides New Insight into the Impacts of Telomeric Cdc13-Stn1-Ten1 Dysfunction on Cell Cycle Progression

Nathalie Grandin, Michel Charbonneau
Cells
DNA Repair Mechanisms
article

The stn1-sz2 Mutant Provides New Insight into the Impacts of Telomeric Cdc13-Stn1-Ten1 Dysfunction on Cell Cycle Progression

Nathalie Grandin, Michel Charbonneau
article en

Abstract

The conserved and essential Cdc13/CTC1-Stn1-Ten1 telomeric complex (CST) ensures chromosome stability by protecting telomere ends and regulating telomerase accessibility. In a recent study, we uncovered mutants of the <i>S</i>. <i>cerevisiae</i> CST, in which damage was sensed by the two major G2/M spindle checkpoints (one is Bub2-dependent and the other one Mad2-dependent), as well as the major G2/M DNA damage checkpoint (Mec1-dependent). In this study, we found, by fluorescence microscopy, that the stability of the mitotic tubulin spindle was profoundly affected in the best-studied of these mutants, <i>stn1</i>-<i>sz2</i>. Additional data from genetic analyses suggested the potential involvement of Stu1 and Stu2, as well as Slk19, in these defects. Throughout this study, we compared the phenotypes of <i>stn1</i>-<i>sz2</i> with those of <i>cdc13</i>-<i>1</i>, the best-studied CST mutant, which also serves as a prototype of telomere-damage-characterized CST mutants. We propose that <i>stn1</i>-<i>sz2</i> represents the prototype of <i>cst</i> mutants characterized by tubulin spindle damage. These newly described phenotypes potentially represent the basis for identifying new functions of the CST telomeric complex. These functions might consist of ensuring correct chromosome segregation through the stabilization of the mitotic spindle.

CellsVol. 14(11)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Clermont Auvergne (FR), Institut Génétique, Reproduction et Développement (FR)
Life in Land
Openalex Percentile: Top 89%
DNA Repair Mechanisms
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