A transient pool of nuclear F-actin at mitotic exit controls chromatin organization.

Abstract:

:Re-establishment of nuclear structure and chromatin organization after cell division is integral for genome regulation or development and is frequently altered during cancer progression. The mechanisms underlying chromatin expansion in daughter cells remain largely unclear. Here, we describe the transient formation of nuclear actin filaments (F-actin) during mitotic exit. These nuclear F-actin structures assemble in daughter cell nuclei and undergo dynamic reorganization to promote nuclear protrusions and volume expansion throughout early G1 of the cell cycle. Specific inhibition of this nuclear F-actin assembly impaired nuclear expansion and chromatin decondensation after mitosis and during early mouse embryonic development. Biochemical screening for mitotic nuclear F-actin interactors identified the actin-disassembling factor cofilin-1. Optogenetic regulation of cofilin-1 revealed its critical role for controlling timing, turnover and dynamics of F-actin assembly inside daughter cell nuclei. Our findings identify a cell-cycle-specific and spatiotemporally controlled form of nuclear F-actin that reorganizes the mammalian nucleus after mitosis.

journal_name

Nat Cell Biol

journal_title

Nature cell biology

authors

Baarlink C,Plessner M,Sherrard A,Morita K,Misu S,Virant D,Kleinschnitz EM,Harniman R,Alibhai D,Baumeister S,Miyamoto K,Endesfelder U,Kaidi A,Grosse R

doi

10.1038/ncb3641

subject

Has Abstract

pub_date

2017-12-01 00:00:00

pages

1389-1399

issue

12

eissn

1465-7392

issn

1476-4679

pii

ncb3641

journal_volume

19

pub_type

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