Tools for live-cell imaging of cytoskeletal and nuclear behavior in the unconventional yeast, Aureobasidium pullulans

Author:

Petrucco Claudia A.1,Crocker Alex W.2,D’Alessandro Alec1,Medina Edgar M.3,Gorman Olivia1,McNeill Jessica1,Gladfelter Amy S.4,Lew Daniel J.1ORCID

Affiliation:

1. Department of Pharmacology and Cancer Biology, Duke University, Durham, NC 27710

2. Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599

3. Department of Biology, University of Massachusetts, Amherst, MA 01003

4. Department of Cell Biology, Duke University, Durham, NC 27710

Abstract

Aureobasidium pullulans is a ubiquitous fungus with a wide variety of morphologies and growth modes including “typical” single-budding yeast, and interestingly, larger multinucleate yeast than can make multiple buds in a single cell cycle. The study of A. pullulans promises to uncover novel cell biology, but currently tools are lacking to achieve this goal. Here, we describe initial components of a cell biology toolkit for A. pullulans, which is used to express and image fluorescent probes for nuclei as well as components of the cytoskeleton. These tools allowed live-cell imaging of the multinucleate and multibudding cycles, revealing highly synchronous mitoses in multinucleate yeast that occur in a semiopen manner with an intact but permeable nuclear envelope. These findings open the door to using this ubiquitous polyextremotolerant fungus as a model for evolutionary cell biology.

Publisher

American Society for Cell Biology (ASCB)

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