Ciliary protein trafficking mediated by IFT and BBSome complexes with the aid of kinesin-2 and dynein-2 motors.

Abstract:

:Cilia and flagella of eukaryotic cells are evolutionarily conserved organelles with a microtubule-based axoneme as a scaffold. To fulfil their functions in cellular motility, sensory reception and developmental signalling, cilia contain unique proteins, such as receptors and ion channels. The assembly and maintenance of cilia depend on protein trafficking mediated by intraflagellar transport (IFT) particles as well as on selective entry and exit of proteins across the transition zone, which is located at the ciliary base. Bidirectional movement of IFT particles, which are composed of IFT-A and IFT-B complexes, is powered by kinesin-2 and dynein-2 motors. The BBSome associates with IFT particles and probably mediates the ciliary trafficking of membrane proteins. Abnormal ciliary assembly and functions due to defects in IFT particle components lead to a wide spectrum of disorders, which are collectively called the ciliopathies. We here review the IFT machinery by associating the architecture of the IFT complexes and their motor and cargo proteins with their functions.

journal_name

J Biochem

journal_title

Journal of biochemistry

authors

Nakayama K,Katoh Y

doi

10.1093/jb/mvx087

subject

Has Abstract

pub_date

2018-03-01 00:00:00

pages

155-164

issue

3

eissn

0021-924X

issn

1756-2651

pii

4765758

journal_volume

163

pub_type

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