Dynein-dependent collection of membranes defines the architecture and position of microtubule asters in isolated, geometrically confined volumes of cell-free extracts

dc.contributor.author Sami, Abdullah Bashar
dc.contributor.author Gatlin, Jesse C.
dc.date.accessioned 2023-02-23T18:56:14Z
dc.date.available 2023-02-23T18:56:14Z
dc.date.issued 2022-09-07
dc.description © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Sami, A. B., & Gatlin, J. C. Dynein-dependent collection of membranes defines the architecture and position of microtubule asters in isolated, geometrically confined volumes of cell-free extracts. Molecular Biology of the Cell, 33(11), (2022): mbcE22030074, https://doi.org/10.1091/mbc.E22-03-0074. en_US
dc.description.abstract It is well established that changes in the underlying architecture of the cell’s microtubule (MT) network can affect organelle organization within the cytoplasm, but it remains unclear whether the spatial arrangement of organelles reciprocally influences the MT network. Here we use a combination of cell-free extracts and hydrogel microenclosures to characterize the relationship between membranes and MTs during MT aster centration. We found that initially disperse ER membranes are collected by the aster and compacted near its nucleating center, all while the whole ensemble moves toward the geometric center of its confining enclosure. Once there, aster MTs adopt a bull’s-eye pattern with a high-density annular ring of MTs surrounding the compacted membrane core of lower MT density. Formation of this pattern was inhibited when dynein-dependent transport was perturbed or when membranes were depleted from the extracts. Asters in membrane-depleted extracts were able to move away from the most proximal wall but failed to center in cylindrical enclosures with diameters greater than or equal to 150 µm. Taken as whole, our data suggest that the dynein-dependent transport of membranes buttresses MTs near the aster center and that this plays an important role in modulating aster architecture and position. en_US
dc.description.sponsorship This work was made possible by an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health (Grant #2P20GM103432). It was also supported by additional funding provided by the NIGMS (Grant #R01GM135568), the Biomedical Scholars program of the Pew Charitable Trusts, and the Marine Biological Laboratory Whitman Center. en_US
dc.identifier.citation Sami, A. B., & Gatlin, J. C. (2022). Dynein-dependent collection of membranes defines the architecture and position of microtubule asters in isolated, geometrically confined volumes of cell-free extracts. Molecular Biology of the Cell, 33(11), mbcE22030074. en_US
dc.identifier.doi 10.1091/mbc.E22-03-0074
dc.identifier.uri https://hdl.handle.net/1912/29710
dc.publisher American Society for Cell Biology en_US
dc.relation.uri https://doi.org/10.1091/mbc.E22-03-0074
dc.rights Attribution-NonCommercial-ShareAlike 4.0 International *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/ *
dc.title Dynein-dependent collection of membranes defines the architecture and position of microtubule asters in isolated, geometrically confined volumes of cell-free extracts en_US
dc.type Article en_US
dspace.entity.type Publication
relation.isAuthorOfPublication 230de64e-ab92-48b2-b68b-7802742b3e82
relation.isAuthorOfPublication 7367d382-34e7-4091-b083-8bba580c7f5b
relation.isAuthorOfPublication.latestForDiscovery 230de64e-ab92-48b2-b68b-7802742b3e82
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