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How Microtubules Build the Spindle Branch by Branch

Author(s): Travis, Sophie M; Mahon, Brian P; Petry, Sabine

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dc.contributor.authorTravis, Sophie M-
dc.contributor.authorMahon, Brian P-
dc.contributor.authorPetry, Sabine-
dc.date.accessioned2023-12-08T18:14:52Z-
dc.date.available2023-12-08T18:14:52Z-
dc.date.issued2022-10-06en_US
dc.identifier.issn1081-0706-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1p843w06-
dc.description.abstractThe microtubule (MT) cytoskeleton provides the architecture that governs intracellular organization and the regulated motion of macromolecules through the crowded cytoplasm. The key to establishing a functioning cytoskeletal architecture is regulating when and where new MTs are nucleated. Within the spindle, the vast majority of MTs are generated through a pathway known as branching MT nucleation, which exponentially amplifies MT number in a polar manner. Whereas other MT nucleation pathways generally require a complex organelle such as the centrosome or Golgi apparatus to localize nucleation factors, the branching site is based solely on a simple, preformed MT, making it an ideal system to study MT nucleation. In this review, we address recent developments in characterizing branching factors, the branching reaction, and its regulation, as well as branching MT nucleation in systems beyond the spindle and within human disease.en_US
dc.languageenen_US
dc.language.isoen_USen_US
dc.relation.ispartofAnnual Review of Cell and Developmental Biologyen_US
dc.rightsAuthor's manuscripten_US
dc.subjectmitosis; meiosis; branching microtubule nucleation; γ-tubulin ring complex; γ-TuRC; augmin; TPX2en_US
dc.titleHow Microtubules Build the Spindle Branch by Branchen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1146/annurev-cellbio-120420-114559-
dc.identifier.eissn1530-8995-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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