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Petrucco, C. A.

Publications and source records attributed to Petrucco, C. A..

3 recordsLinked to original sources

A G2 Checkpoint Arrests Cryptococcus neoformans Cell Division in response to Hypoxia

Saturated cultures of the pathogenic yeast, Cryptococcus neoformans, arrest as unbudded cells in the G2 phase of the cell cycle. As cells divided and cultures saturated, we found that oxygen levels in the culture medium dropped nearly tenfold. When saturation-arrested cultures were re-oxygenated without adding fresh growth medium, cells immediately formed a bud and then underwent mitosis. Thus, the arrest is due to low oxygen concentration rather than nutrient depletion. Because the G2 arrest was associated with unbudded cells, we asked whether C. neoformans cells have a morphogenesis checkpoint that blocks mitosis until cells can form a bud. Inhibition of budding by treatment with Latrunculin A also led to G2 arrest, and we determined that this arrest is dependent on the CDK inhibitory kinase, Swe1. This finding suggests that C. neoformans possesses a morphogenesis checkpoint analogous to that in the distantly related Saccharomyces cerevisiae. We also demonstrated that Swe1 is required to enforce the hypoxia-induced G2 arrest. We propose that hypoxia inhibits budding in C. neoformans, which in turn triggers a morphogenesis checkpoint to arrest cells in G2 even when nutrients are plentiful.

cell biology↗

Mechanisms of nuclear segregation in a multinucleate multibudding yeast

Budding yeasts present an especially challenging geometry for segregation of chromosomes, which must be delivered across the narrow mother-bud neck into the bud. Studies in the model yeast Saccharomyces cerevisiae have revealed an elaborate set of mechanisms that selectively orient one mitotic spindle pole towards the bud and then drive spindle elongation along the mother-bud axis, ensuring nuclear segregation between mother and bud. It is unclear how these pathways might be adapted to yield similar precision in more complex cell geometries. Here we provide the first description of the dynamics of mitosis in a multi-nucleate, multibudding yeast, Aureobasidium pullulans, and identify many unexpected differences from uninucleate yeasts. Mitotic spindles do not orient along the mother-bud axis prior to anaphase, and accurate nuclear segregation often occurs after spindle disassembly. Cortical Num1-dynein forces pull highly mobile nuclei into buds, and once a nucleus enters a bud, it discourages others from entering, ensuring that most daughters inherit only one nucleus.

cell biology↗

Negative feedback equalizes polarity sites in a multi-budding yeast

Morphogenesis in fungi and animals is directed by polarization of small GTPases Cdc42 and Rac. In the budding yeast Saccharomyces cerevisiae competition between polarity patches results in one polarized patch and the growth of a single bud. Here, we describe cell polarity in the yeast Aureobasidium pullulans, which establishes multiple coexisting polarity sites yielding multiple buds during a single cell division cycle. Polarity machinery components oscillate in their abundance in these coexisting sites but do so independently of one another, pointing to a lack of global coupling between sites. Previous theoretical work has demonstrated that negative feedback in a polarity circuit could promote coexistence of multiple polarity sites, and time-delayed negative feedback is known to cause oscillations. We show that both these features of negative feedback depend on a protein we identified as Pak1, and that Pak1 requires Rac1 but not Cdc42 for its localization. This work shows how conserved signaling networks can be modulated for distinct morphogenic programs even within the constraints of fungal budding.

cell biology↗