Fidgetin regulates cultured astrocyte migration by severing tyrosinated microtubules at the leading edge.

Abstract:

:Microtubule (MT) organization is essential for many cellular events, including mitosis, migration, and cell polarity. Fidgetin (Fign), an ATP-dependent, MT-severing protein, contributes to the regulation of MT configuration by cutting and trimming MT polymers. Functions of Fign have been indicated in neurite outgrowth, mitosis, meiosis, and cellular migration. Here we focus on migration of astrocytes. We find that Fign plays an essential role in cultured astrocyte migration by preferentially targeting MTs (or regions of MTs) that are rich in tyrosinated tubulin, a marker for especially dynamic MTs or especially dynamic regions of MTs. Inhibition of cellular migration induced by Fign knockdown can be rescued with concomitant knockdown of kinesin-12, a motor protein best known for its role in mitosis. We propose a novel working model for MT reconfiguration underlying cellular migration elicited by the functional cooperation of two distinct MT-related proteins.

journal_name

Mol Biol Cell

authors

Hu Z,Feng J,Bo W,Wu R,Dong Z,Liu Y,Qiang L,Liu M

doi

10.1091/mbc.E16-09-0628

subject

Has Abstract

pub_date

2017-02-15 00:00:00

pages

545-553

issue

4

eissn

1059-1524

issn

1939-4586

pii

mbc.E16-09-0628

journal_volume

28

pub_type

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