Activity of Rho-family GTPases during cell division as visualized with FRET-based probes

被引:331
作者
Yoshizaki, H
Ohba, Y
Kurokawa, K
Itoh, RE
Nakamura, T
Mochizuki, N
Nagashima, K
Matsuda, M [1 ]
机构
[1] Osaka Univ, Res Inst Microbial Dis, Dept Tumor Virol, Suita, Osaka 5650871, Japan
[2] Japan Sci & Technol Cooperat, Core Res Evolut Sci & Technol, Fukuoka 8168580, Japan
[3] Natl Cardiovasc Ctr Hosp & Res Inst, Dept Struct Anal, Osaka 5658565, Japan
[4] Hokkaido Univ, Sch Med, Lab Mol & Cellular Pathol, Sapporo, Hokkaido 0608638, Japan
关键词
fluorescent probes; cytokinesis; rho GTP-binding proteins; rac GTP-binding proteins; Cdc42 GTP-binding protein;
D O I
10.1083/jcb.200212049
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rho-family GTPases regulate many cellular functions. To visualize the activity of Rho-family GTPases in living cells, we developed fluorescence resonance energy transfer (FRET)-based probes for Rac1 and Cdc42 previously (Itoh, R.E., K. Kurokawa, Y. Ohba, H. Yoshizaki, N. Mochizuki, and M. Matsuda. 2002. Mol. Cell. Biol. 22:6582-6591). Here, we added two types of probes for RhoA. One is to monitor the activity balance between guanine nucleotide exchange factors and GTPase-activating proteins, and another is to monitor the level of GTP-RhoA. Using these FRET probes, we imaged the activities of Rho-family GTPases during the cell division of HeLa cells. The activities of RhoA, Rac1, and Cdc42 were high at the plasma membrane in interphase, and decreased rapidly on entry into M phase. From after anaphase, the RhoA activity increased at the plasma membrane including cleavage furrow. Rac1 activity was suppressed at the spindle midzone and increased at the plasma membrane of polar sides after telophase. Cdc42 activity was suppressed at the plasma membrane and was high at the intracellular membrane compartments during cytokinesis. In conclusion, we could use the FRET-based probes to visualize the complex spatio-temporal regulation of Rho-family GTPases during cell division.
引用
收藏
页码:223 / 232
页数:10
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