Cortical dynamics during cell motility are regulated by CRL3KLHL21 E3 ubiquitin ligase

Cortical dynamics during cell motility are regulated by CRL3KLHL21 E3 ubiquitin ligase

Directed cell movement involves spatial and temporal regulation of the cortical microtubule (Mt) and actin networks to allow focal adhesions (FAs) to assemble at the cell front and disassemble at the rear. Mts are known to associate with FAs, but the mechanisms coordinating their dynamic interaction...

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Bibliographic Details
Published in:Nature communications Vol. 7; no. 1; pp. 12810 - 13
Main Authors: Courtheoux, Thibault, Enchev, Radoslav I., Lampert, Fabienne, Gerez, Juan, Beck, Jochen, Picotti, Paola, Sumara, Izabela, Peter, Matthias
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 19-09-2016
Nature Publishing Group
Nature Portfolio
Subjects:
14/35
14/63
631/80/128/1653
631/80/84/2027
Cell adhesion & migration
Enzymes
Humanities and Social Sciences
Kinases
Life Sciences
Motility
multidisciplinary
Proteins
Science
Science (multidisciplinary)
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Summary:Directed cell movement involves spatial and temporal regulation of the cortical microtubule (Mt) and actin networks to allow focal adhesions (FAs) to assemble at the cell front and disassemble at the rear. Mts are known to associate with FAs, but the mechanisms coordinating their dynamic interactions remain unknown. Here we show that the CRL3 KLHL21 E3 ubiquitin ligase promotes cell migration by controlling Mt and FA dynamics at the cell cortex. Indeed, KLHL21 localizes to FA structures preferentially at the leading edge, and in complex with Cul3, ubiquitylates EB1 within its microtubule-interacting CH-domain. Cells lacking CRL3 KLHL21 activity or expressing a non-ubiquitylatable EB1 mutant protein are unable to migrate and exhibit strong defects in FA dynamics, lamellipodia formation and cortical plasticity. Our study thus reveals an important mechanism to regulate cortical dynamics during cell migration that involves ubiquitylation of EB1 at focal adhesions. Although focal adhesions (FAs) and microtubules (MTs) are known to associate, the underlying regulation of this dynamic interaction is not understood. Here the authors discover that the CRL3 KLHL21 E3 ubiquitin ligase localises to FAs and ubiquitinates the MT plus-tip binding protein EB1, thereby promoting MT and FA dynamics and cell migration.
Bibliography:PMCID: PMC5031805
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms12810