Document Type
Article
Publication Date
7-2022
Publisher
MDPI
Source Publication
Viruses
Source ISSN
1999-4915
Original Item ID
DOI: 10.3390/v14071581
Abstract
Yeast prions are self-perpetuating misfolded proteins that are infectious. In yeast, [PSI+] is the prion form of the Sup35 protein. While the study of [PSI+] has revealed important cellular mechanisms that contribute to prion propagation, the underlying cellular factors that influence prion formation are not well understood. Prion formation has been described as a multi-step process involving both the initial nucleation and growth of aggregates, followed by the subsequent transmission of prion particles to daughter cells. Prior evidence suggests that actin plays a role in this multi-step process, but actin’s precise role is unclear. Here, we investigate how actin influences the cell’s ability to manage newly formed visible aggregates and how actin influences the transmission of newly formed aggregates to future generations. At early steps, using 3D time-lapse microscopy, several actin mutants, and Markov modeling, we find that the movement of newly formed aggregates is random and actin independent. At later steps, our prion induction studies provide evidence that the transmission of newly formed prion particles to daughter cells is limited by the actin cytoskeletal network. We suspect that this limitation is because actin is used to possibly retain prion particles in the mother cell.
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Recommended Citation
Dorweiler, Jane E.; Lyke, Douglas R.; LeMoine, Nathan P.; Guereca, Samantha; Buchholz, Hannah E.; Legan, Emily R.; Radtke, Claire M.; and Manogaran, Anita L., "Implications of the Actin Cytoskeleton on the Multi-Step Process of [ PSI+] Prion Formation" (2022). Biological Sciences Faculty Research and Publications. 888.
https://epublications.marquette.edu/bio_fac/888
Comments
Published version. Viruses, Vol. 14, No. 1 (July 2022): 1581. DOI. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. Used with permission.