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Updated: Jun 12, 2026

Using Ustilago maydis as a Trojan Horse for In Situ Delivery of Maize Proteins
Published on: February 8, 2019
Role of the nuclear migration protein Lis1 in cell morphogenesis in Ustilago maydis
Michael Valinluck1, Sara Ahlgren, Mizuho Sawada
1Department of Biological Sciences, California State University, 1250 Bellflower Boulevard, Long Beach, California 90840 USA.
Abstract:
Ustilago maydis is a basidiomycete fungus that exhibits a yeast-like and a filamentous form. Growth of the fungus in the host leads to additional morphological transitions. The different morphologies are characterized by distinct nuclear movements. Dynein and alpha-tubulin are required for nuclear movements and for cell morphogenesis of the yeast-like form. Lis1 is a microtubule plus-end tracking protein (+TIPs) conserved in eukaryotes and required for nuclear migration and spindle positioning. Defects in nuclear migration result in altered cell fate and aberrant development in metazoans, slow growth in fungi and disease in humans (e.g. lissencephaly). Here we investigate the role of the human LIS1 homolog in U. maydis and demonstrate that it is essential for cell viability, not previously seen in other fungi. With a conditional null mutation we show that lis1 is necessary for nuclear migration in the yeast-like cell and during the dimorphic transition. Studies of asynchronous exponentially growing cells and time-lapse microscopy uncovered novel functions of lis1: It is necessary for cell morphogenesis, positioning of the septum and cell wall integrity. lis1-depleted cells exhibit altered axes of growth and loss of cell polarity leading to grossly aberrant cells with clusters of nuclei and morphologically altered buds devoid of nuclei. Altered septum positioning and cell wall deposition contribute to the aberrant morphology. lis1-depleted cells lyse, indicative of altered cell wall properties or composition. We also demonstrate, with indirect immunofluorescence to visualize tubulin, that lis1 is necessary for the normal organization of the microtubule cytoskeleton: lis1-depleted cells contain more and longer microtubules that can form coils perpendicular to the long axis of the cell. We propose that lis1 controls microtubule dynamics and thus the regulated delivery of vesicles to growth sites and other cell domains that govern nuclear movements.
Insights
The human LIS1 gene is crucial for the survival and proper cell structure of Ustilago maydis, a fungus. It regulates nuclear migration, cell shape, and microtubule organization, with its depletion causing cell death.
Area of Science:
- Mycology
- Cell Biology
- Genetics
Background:
- Ustilago maydis exhibits yeast-like and filamentous forms with distinct nuclear movements.
- Microtubule-associated proteins like Dynein and alpha-tubulin are vital for nuclear migration and cell morphogenesis.
- Lis1, a conserved eukaryotic protein, is essential for nuclear migration and spindle positioning, with defects linked to developmental abnormalities and diseases.
Purpose of the Study:
- To investigate the role of the human LIS1 homolog in Ustilago maydis.
- To determine if LIS1 is essential for U. maydis viability and cellular processes.
- To elucidate novel functions of LIS1 in fungal cell morphogenesis and nuclear dynamics.
Main Methods:
- Conditional null mutation of the LIS1 gene in U. maydis.
- Time-lapse microscopy to observe cell behavior and nuclear migration.
- Indirect immunofluorescence to visualize microtubule cytoskeleton organization.
Main Results:
- LIS1 is essential for U. maydis cell viability, a novel finding in fungi.
- LIS1 is required for nuclear migration during yeast-like growth and dimorphic transition.
- LIS1 depletion leads to aberrant cell morphogenesis, septum positioning, loss of polarity, and cell lysis due to altered microtubule dynamics and cell wall integrity.
Conclusions:
- Human LIS1 homolog is indispensable for U. maydis cell viability and development.
- LIS1 plays critical roles in nuclear migration, cell polarity, and morphogenesis.
- LIS1 likely controls microtubule dynamics, impacting vesicle transport and cellular organization.
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