FHOD1 interaction with nesprin-2G mediates TAN line formation and nuclear movement

被引:85
作者
Kutscheidt, Stefan [1 ]
Zhu, Ruijun [2 ]
Antoku, Susumu [2 ]
Luxton, G. W. Gant [2 ]
Stagljar, Igor [3 ]
Fackler, Oliver T. [1 ]
Gundersen, Gregg G. [2 ]
机构
[1] Univ Heidelberg Hosp, Dept Infect Dis, D-69120 Heidelberg, Germany
[2] Columbia Univ, Dept Pathol & Cell Biol, New York, NY 10032 USA
[3] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada
关键词
ACTIN STRESS FIBERS; FORMIN FHOD1; CENTROSOME ORIENTATION; F-ACTIN; MIGRATION; MICROTUBULES; ACTIVATION; FLOW; STABILIZATION; REORIENTATION;
D O I
10.1038/ncb2981
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Active positioning of the nucleus is integral to division, migration and differentiation of mammalian cells(1). Fibroblasts polarizing for migration orient their centrosomes by actin-dependent nuclear movement(2). This nuclear movement depends on nesprin-2 giant (N2G), a large, actin-binding outer nuclear membrane component of transmembrane actin-associated (TAN) lines that couple nuclei to moving actin cables(3). Here, we identify the diaphanous formin FHOD1 as an interaction partner of N2G. Silencing FHOD1 expression or expression of fragments containing binding sites for N2G or FHOD1 disrupted nuclear movement and centrosome orientation in polarizing fibroblasts. Unexpectedly, silencing of FHOD1 expression did not affect the formation or rearward flow of dorsal actin cables required for nuclear positioning. Rather, N2G-FHOD1 interaction provided a second connection to actin cables essential for TAN line formation and thus nuclear movement. These results reveal a unique function for a formin in coupling an organelle to actin filaments for translocation, and suggest that TAN lines require multi-point attachments to actin cables to resist the large forces necessary to move the nucleus.
引用
收藏
页码:708 / +
页数:17
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