Actin-related protein Arp4 functions in kinetochore assembly

被引:29
|
作者
Ogiwara, Hideaki
Ui, Ayako
Kawashima, Satoshi
Kugou, Kazuto
Onoda, Fumitoshi
Iwahashi, Hitoshi
Harata, Masahiko
Ohta, Kunihiro
Enomoto, Takemi
Seki, Masayuki
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Mol Cell Biol Lab, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] RIKEN, Genet Syst Regulat Lab, Wako, Saitama 3510198, Japan
[3] Saitama Univ, Grad Sch Sci & Engn, Sakura Ku, Saitama, Saitama 3388570, Japan
[4] Natl Inst Adv Ind Sci & Technol, Tsukuba, Japan
[5] Tohoku Univ, Grad Sch Agr Sci, Sendai, Miyagi 9818555, Japan
[6] Tohoku Univ, 21st Century COE Program, Comprehens Res & Educ Ctr Planning Drug Dev & Cli, Sendai, Miyagi 9808578, Japan
关键词
D O I
10.1093/nar/gkm161
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
The actin- related proteins ( Arps) comprise a conserved protein family. Arp4p is found in large multisubunits of the INO80 and SWR1 chromatin remodeling complexes and in the NuA4 histone acetyltransferase complex. Here we show that arp4 ( arp4S23A/ D159A) temperature- sensitive cells are defective in G2/ M phase function. arp4 mutants are sensitive to the microtubule depolymerizing agent benomyl and arrest at G2/ M phase at restrictive temperature. Arp4p is associated with centromeric and telomeric regions throughout cell cycle. Ino80p, Esa1p and Swr1p, components of the INO80, NuA4 and SWR1 complexes, respectively, also associate with centromeres. The association of many kinetochore components including Cse4p, a component of the centromere nucleosome, Mtw1p and Ctf3p is partially impaired in arp4 cells, suggesting that the G2/ M arrest of arp4 mutant cells is due to a defect in formation of the chromosomal segregation apparatus.
引用
收藏
页码:3109 / 3117
页数:9
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