4.5 Article

Proximity-dependent Proteomics Reveals Extensive Interactions of Protocadherin-19 with Regulators of Rho GTPases and the Microtubule Cytoskeleton

Journal

NEUROSCIENCE
Volume 452, Issue -, Pages 26-36

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2020.09.033

Keywords

cell adhesion; protocadherin; proteomics

Categories

Funding

  1. National Science Foundation [IOS 1457126]
  2. NIH [R01 EY027003, S10 OD010383, S10 OD18056]
  3. NIH Neurosciences Center Core Grant [P30 NS104177]

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This study investigated the role of Pcdh19 in nervous system development, revealing interactions with proteins that regulate Rho family GTPases, microtubule binding proteins, and cell divisions. These findings provide important insights for future investigations into the cellular and molecular biology of Pcdh19.
belongs to the cadherin family of cell surface receptors and has been shown to play essential roles in the development of the vertebrate nervous system. Mutations in human Protocadherin-19 (PCDH19) lead to PCDH19 Female-limited epilepsy (PCDH19 FLE) in humans, characterized by the early onset of epileptic seizures in children and a range of cognitive and behavioral problems in adults. Despite being considered the second most prevalent gene in epilepsy, very little is known about the intercellular pathways in which it participates. In order to characterize the protein complexes within which Pcdh19 functions, we generated Pcdh19-BioID fusion proteins and utilized proximity-dependent biotinylation to identify neighboring proteins. Proteomic identification and analysis revealed that the Pcdh19 interactome is enriched in proteins that regulate Rho family GTPases, microtubule binding proteins and proteins that regulate cell divisions. We cloned the centrosomal protein Nedd1 and the RacGEF Dock7 and verified their interactions with Pcdh19 in vitro. Our findings provide the first comprehensive insights into the interactome of Pcdh19, and provide a platform for future investigations into the cellular and molecular biology of this protein critical to the proper development of the nervous system. (C) 2020 IBRO. Published by Elsevier Ltd. All rights reserved.

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