Literature DB >> 30205038

WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation.

Saurabh S Kulkarni1, John N Griffin1, Priya P Date1, Karel F Liem2, Mustafa K Khokha3.   

Abstract

The actin cytoskeleton is critical to shape cells and pattern intracellular organelles, which collectively drives tissue morphogenesis. In multiciliated cells (MCCs), apical actin drives expansion of the cell surface necessary to host hundreds of cilia. The apical actin also forms a lattice to uniformly distribute basal bodies. This apical actin network is dynamically remodeled, but the molecules that regulate its architecture remain poorly understood. We identify the chromatin modifier, WDR5, as a regulator of apical F-actin in MCCs. Unexpectedly in MCCs, WDR5 has a function independent of chromatin modification. We discover a scaffolding role for WDR5 between the basal body and F-actin. Specifically, WDR5 binds to basal bodies and migrates apically, where F-actin organizes around WDR5. Using a monomer trap for G-actin, we show that WDR5 stabilizes F-actin to maintain lattice architecture. In summary, we identify a non-chromatin role for WDR5 in stabilizing F-actin in MCCs.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  H3K4; Xenopus; basal body; cilia; congenital heart disease; histone modifier; methylation

Mesh:

Substances:

Year:  2018        PMID: 30205038      PMCID: PMC6177229          DOI: 10.1016/j.devcel.2018.08.009

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  67 in total

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