Asymmetric microtubule pushing forces in nuclear centering

被引:72
作者
Daga, Rafael R. [1 ]
Yonetani, Ann [1 ]
Chang, Fred [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Microbiol, New York, NY 10032 USA
关键词
D O I
10.1016/j.cub.2006.06.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dynamic properties of microtubules contribute to the establishment of spatial order within cells. In the fission yeast Schizosaccharomyces pombe, interphase cytoplasmic microtubules are organized into antiparallel bundles that attach to the nuclear envelope and are needed to position the nucleus at the geometric center of the cell [1, 2]. Here, we show that after the nucleus is displaced by cell centrifugation, these microtubule bundles efficiently push the nucleus back to the center. Asymmetry in microtubule number, length, and dynamics contributes to the generation of force responsible for this unidirectional movement. Notably, microtubules facing the distal cell tip are destabilized when the microtubules in the same bundle are pushing from the proximal cell tip. The CLIP-170-like protein tip1p [3] and the microtubule-bundling proteinase1p [4,5] are required for this asymmetric regulation of microtubule dynamics, indicating contributions of factors both at microtubule plus ends and within the microtubule bundle. Mutants in these factors are defective in nuclear movement. Thus, cells possess an efficient microtubule-based engine that produces and senses forces for centering the nucleus. These studies may provide insights into mechanisms of asymmetric microtubule behaviors and force sensing in other processes such as chromosome segregation and cell polarization.
引用
收藏
页码:1544 / 1550
页数:7
相关论文
共 24 条
[1]   CLIP170-like tip1p spatially organizes microtubular dynamics in fission yeast [J].
Brunner, D ;
Nurse, P .
CELL, 2000, 102 (05) :695-704
[2]   The microtubule plus end-tracking proteins mal3p and tip1p cooperate for cell-end targeting of interphase microtubules [J].
Busch, KE ;
Brunner, D .
CURRENT BIOLOGY, 2004, 14 (07) :548-559
[3]   Tea2p kinesin is involved in spatial microtubule organization by transporting Tip1p on microtubules [J].
Busch, KE ;
Hayles, J ;
Nurse, P ;
Brunner, D .
DEVELOPMENTAL CELL, 2004, 6 (06) :831-843
[4]   Determining the position of the cell division plane [J].
Canman, JC ;
Cameron, LA ;
Maddox, PS ;
Straight, A ;
Tirnauer, JS ;
Mitchison, TJ ;
Fang, GW ;
Kapoor, TM ;
Salmon, ED .
NATURE, 2003, 424 (6952) :1074-1078
[5]   The kinesin Klp2 mediates polarization of interphase microtubules in fission yeast [J].
Carazo-Salas, RE ;
Antony, C ;
Nurse, P .
SCIENCE, 2005, 309 (5732) :297-300
[6]   Dynamic positioning of the fission yeast cell division plane [J].
Daga, RR ;
Chang, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (23) :8228-8232
[7]   Dynamics of interphase microtubules in Schizosaccharomyces pombe [J].
Drummond, DR ;
Cross, RA .
CURRENT BIOLOGY, 2000, 10 (13) :766-775
[8]   Regulation of a formin complex by the microtubule plus end protein tea1p [J].
Feierbach, B ;
Verde, F ;
Chang, F .
JOURNAL OF CELL BIOLOGY, 2004, 165 (05) :697-707
[9]   Evolutionary conservation of microtubule-capture mechanisms [J].
Gundersen, GG .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (04) :296-304
[10]  
Hagan I, 1997, J CELL SCI, V110, P1851