Quantification of Aspergillus nidulans Actin Dynamics during Early Growth and Septum Formation

dc.contributor.authorHuso, Walker
dc.contributor.authorHill, Garrett
dc.contributor.authorTarimala, Greeshma
dc.contributor.authorLee, Jiyon
dc.contributor.authorDoan, Alexander G.
dc.contributor.authorLee, JungHun
dc.contributor.authorGray, Kelsey
dc.contributor.authorEdwards, Harley
dc.contributor.authorHarris, Steven D.
dc.contributor.authorMarten, Mark
dc.date.accessioned2026-02-12T16:44:51Z
dc.date.issued2026-01-28
dc.description.abstractFilamentous fungi have complex, three-dimensional growth patterns and a non-adherent nature, which can present challenges for live-cell imaging for quantitative assessment of dynamic cellular processes. To address these challenges, a live-cell imaging system has been modified to constrain the model fungus Aspergillus nidulans to growth in a single focal plane. This enables high-resolution time-lapse imaging of actin dynamics throughout development using a Lifeact actin marker. This system was used to perform kymographic analysis to quantify actin velocity and hyphal extension rates during early hyphal development. Results show two distinct growth phases: germ tube extension (0.58 ?m/min) and hyphal extension (1.52 ?m/min). Actin exhibited bi-directional transport along hyphae with biased movement toward the spore body. Actin was also observed re-localizing from hyphal tips to sites of septum formation indicating active redistribution of cytoskeletal resources based on cellular demands. This technological advancement overcomes longstanding limitations in fungal live-cell imaging and provides a new platform for quantitative systems-level analysis of mycelial development, offering new insights into the spatiotemporal coordination of cytoskeletal dynamics during filamentous growth.
dc.description.sponsorshipThis work was supported by the National Science Foundation (Awards 2006189, 2527369, 2527370). We gratefully acknowledge Dr. Tagide deCarvalho and the Keith R. Porter Imaging Facility for the use of the Confocal microscope. We also acknowledge Dr. Govind Rao (UMBC,
dc.description.urihttps://www.biorxiv.org/content/10.64898/2026.01.27.701996v1
dc.format.extent12 pages
dc.genrejournal articles
dc.genrepreprints
dc.identifier.urihttps://doi.org/10.64898/2026.01.27.701996
dc.identifier.urihttp://hdl.handle.net/11603/41962
dc.language.isoen
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Dresher Center for the Humanities
dc.relation.ispartofUMBC Student Collection
dc.relation.ispartofUMBC Chemistry & Biochemistry Department
dc.relation.ispartofUMBC Meyerhoff Scholars Program
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department
dc.relation.ispartofUMBC Education Department
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.en
dc.subjectUMBC MartenLab College of Engineering and Information Technology
dc.subjectUMBC Howard Hughes Medical Institute
dc.titleQuantification of Aspergillus nidulans Actin Dynamics during Early Growth and Septum Formation
dc.typeText
dcterms.creatorhttps://orcid.org/0009-0009-6160-3706
dcterms.creatorhttps://orcid.org/0009-0000-4707-1779
dcterms.creatorhttps://orcid.org/0009-0000-2814-8443
dcterms.creatorhttps://orcid.org/0009-0008-6972-1865
dcterms.creatorhttps://orcid.org/0000-0003-2940-1476
dcterms.creatorhttps://orcid.org/0000-0003-4110-1687
dcterms.creatorhttps://orcid.org/0000-0002-1863-8956
dcterms.creatorhttps://orcid.org/0009-0004-8522-7219

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