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Number Dependence of Microtubule Collective Transport by Kinesin and Dynein

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dc.contributor.author JAIN, KUNALIKA en_US
dc.contributor.author YADAV, SHIVANI A. en_US
dc.contributor.author ATHALE, CHAITANYA A. en_US
dc.date.accessioned 2021-02-05T05:55:59Z
dc.date.available 2021-02-05T05:55:59Z
dc.date.issued 2021-01 en_US
dc.identifier.citation Journal of the Indian Institute of Science, 101, 19-30. en_US
dc.identifier.issn 0019-4964 en_US
dc.identifier.issn 0970-4140 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5580
dc.identifier.uri https://doi.org/10.1007/s41745-020-00212-2 en_US
dc.description.abstract Translational motors that depend on cytoskeletal elements, either actin or tubulin, for their activity are critical for cellular function in eukaryotes. Microtubule (MT)-dependent motors are broadly classified as dyneins and kinesins, based on sequence similarity. Typically, dyneins walk towards the minus-ends of MTs, while kinesins walk towards the plus-ends, with some plant and animal kinesins also seen to be minus-end directed. While our understanding of motor mechanics at a single-molecule level has rapidly improved due to developments in force spectroscopy, in vivo motor transport often involves multiple motors acting together. Here, we review our current understanding of collective effects that emerge in motor-driven transport in vivo based on physical mechanisms inferred from in vitro reconstitution experiments involving MT transport, or ‘gliding assays’. We discuss the evidence for number dependence in cargo transport at MT cross-overs, orientation sorting of MTs during axonal regeneration in neurons, spindle bipolarization by MT transport, and nuclear positioning during mitosis in the model yeasts Saccharomyces cerevisiae and Schizosaccharomyces pombe. We discuss how minimal in vitro gliding assays have been successfully used to identify the mechanical properties of collective motor transport that produce such cooperative effects. The ‘loose coupling’ mechanism of Oosawa, which was developed to explain the emergence of cooperation in collective motor transport, appears to be consistent with evidence from kinesin, but not dynein. Additionally, substrate rigidity also appears to play a role in collective force generation, as seen in lipid-anchorage studies of collective transport. Thus, a deeper understanding of the intra- and inter-motor properties of kinesins and dyneins, as well as non-motor effects due to the substrate is required, for the emergence of a complete picture of the in vivo mechanobiology of collective motor transport. en_US
dc.language.iso en en_US
dc.publisher Springer Nature en_US
dc.subject Biology en_US
dc.subject 2021-FEB-WEEK1 en_US
dc.subject TOC-FEB-2021 en_US
dc.subject 2021 en_US
dc.title Number Dependence of Microtubule Collective Transport by Kinesin and Dynein en_US
dc.type Article en_US
dc.contributor.department Dept. of Biology en_US
dc.identifier.sourcetitle Journal of the Indian Institute of Science en_US
dc.publication.originofpublisher Indian en_US


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