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Sci Rep. 2016 Jun 7;6:27456. doi: 10.1038/srep27456.

Tumour Suppressor Adenomatous Polyposis Coli (APC) localisation is regulated by both Kinesin-1 and Kinesin-2.

Author information

1
Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester, M13 9PT, UK.
2
Division of Cell Biology, Faculty of Science, University of Utrecht, Padualaan 8, 3584CH, Utrecht, The Netherlands.

Abstract

Microtubules and their associated proteins (MAPs) underpin the polarity of specialised cells. Adenomatous polyposis coli (APC) is one such MAP with a multifunctional agenda that requires precise intracellular localisations. Although APC has been found to associate with kinesin-2 subfamily members, the exact mechanism for the peripheral localization of APC remains unclear. Here we show that the heavy chain of kinesin-1 directly interacts with the APC C-terminus, contributing to the peripheral localisation of APC in fibroblasts. In rat hippocampal neurons the kinesin-1 binding domain of APC is required for its axon tip enrichment. Moreover, we demonstrate that APC requires interactions with both kinesin-2 and kinesin-1 for this localisation. Underlining the importance of the kinesin-1 association, neurons expressing APC lacking kinesin-1-binding domain have shorter axons. The identification of this novel kinesin-1-APC interaction highlights the complexity and significance of APC localisation in neurons.

PMID:
27272132
PMCID:
PMC4895226
DOI:
10.1038/srep27456
[Indexed for MEDLINE]
Free PMC Article

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