| Literature DB >> 29348205 |
Matthew T Swulius1,2, Lam T Nguyen1,2, Mark S Ladinsky1, Davi R Ortega1,2, Samya Aich3, Mithilesh Mishra3, Grant J Jensen4,2.
Abstract
Cell division in many eukaryotes is driven by a ring containing actin and myosin. While much is known about the main proteins involved, the precise arrangement of actin filaments within the contractile machinery, and how force is transmitted to the membrane, remains unclear. Here we use cryosectioning and cryofocused ion beam milling to gain access to cryopreserved actomyosin rings in Schizosaccharomyces pombe for direct 3D imaging by electron cryotomography. Our results show that straight, overlapping actin filaments, running nearly parallel to each other and to the membrane, form a loose bundle of ∼150 nm in diameter that "saddles" the inward-bending membrane at the leading edge of the division septum. The filaments do not make direct contact with the membrane. Our analysis of the actin filaments reveals the variability in filament number, nearest-neighbor distances between filaments within the bundle, their distance from the membrane, and angular distribution with respect to the membrane.Entities:
Keywords: FIB mill; actomyosin ring; cell division; cryoEM; cytokinesis
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Year: 2018 PMID: 29348205 PMCID: PMC5816141 DOI: 10.1073/pnas.1711218115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205