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Updated: Aug 11, 2026

Manipulation and Analysis of Cell Cycle-Dependent Processes in Budding Yeast
Published on: September 26, 2025
The Cdc14p phosphatase affects late cell-cycle events and morphogenesis in Candida albicans
Andrés Clemente-Blanco1, Alberto González-Novo, Félix Machín
1Departamento de Microbiología, Facultad de Ciencias, Universidad de Extremadura, Avda Elvas SN, 06071, Badajoz, Spain.
Abstract:
We have characterized the CDC14 gene, which encodes a dual-specificity protein phosphatase in Candida albicans, and demonstrated that its deletion results in defects in cell separation, mitotic exit and morphogenesis. The C. albicans cdc14delta mutants formed large aggregates of cells that resembled those found in ace2-null strains. In cdc14delta cells, expression of Ace2p target genes was reduced and Ace2p did not accumulate specifically in daughter nuclei. Taken together, these results imply that Cdc14p is required for the activation and daughter-specific nuclear accumulation of Ace2p. Consistent with a role in cell separation, Cdc14p was targeted to the septum region during the M-G1 transition in yeast-form cells. Interestingly, hypha-inducing signals abolished the translocation of Cdc14p to the division plate, and this regulation depended on the cyclin Hgc1p, since hgc1delta mutants were able to accumulate Cdc14p in the septum region of the germ tubes. In addition to its role in cytokinesis, Cdc14p regulated mitotic exit, since synchronous cultures of cdc14delta cells exhibited a severe delay in the destruction of the mitotic cyclin Clb2p. Finally, deletion of CDC14 resulted in decreased invasion of solid agar medium and impaired true hyphal growth.
Insights
The CDC14 gene in Candida albicans is crucial for cell separation and proper cell cycle progression. Its absence disrupts Ace2p function, leading to cell aggregation and impaired hyphal growth.
Area of Science:
- * Molecular biology
- * Cell biology
- * Mycology
Background:
- * Candida albicans is an opportunistic fungal pathogen.
- * Cellular processes like cell separation, mitotic exit, and morphogenesis are vital for fungal development and virulence.
- * The CDC14 gene encodes a dual-specificity protein phosphatase, a class of enzymes involved in cell cycle regulation.
Purpose of the Study:
- * To characterize the function of the CDC14 gene in Candida albicans.
- * To investigate the role of Cdc14p in cell separation, mitotic exit, and morphogenesis.
- * To elucidate the relationship between Cdc14p, Ace2p, and hyphal growth regulation.
Main Methods:
- * Gene deletion to create cdc14delta mutants.
- * Analysis of cell aggregation and morphology.
- * Gene expression analysis of Ace2p target genes.
- * Microscopy to observe protein localization (Cdc14p, Ace2p).
- * Cell cycle analysis to assess mitotic exit and cyclin destruction.
Main Results:
- * Deletion of CDC14 in C. albicans resulted in significant defects in cell separation, leading to cell aggregation.
- * cdc14delta mutants showed impaired mitotic exit, evidenced by delayed Clb2p destruction.
- * Cdc14p is essential for the activation and daughter-nucleus-specific accumulation of Ace2p.
- * Cdc14p localization to the septum during cytokinesis is regulated by hypha-inducing signals and Hgc1p.
- * Loss of CDC14 function impaired true hyphal growth and invasion of agar medium.
Conclusions:
- * Cdc14p plays a critical role in regulating cell separation and mitotic exit in Candida albicans.
- * Cdc14p is required for the proper function and localization of the transcription factor Ace2p.
- * Regulation of Cdc14p localization is influenced by hyphal growth pathways, indicating its integration into developmental signaling.
- * CDC14 is a key determinant of C. albicans morphogenesis and virulence-associated traits like hyphal growth.
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