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.
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21 July 2003
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July 08 2003
Activity of Rho-family GTPases during cell division as visualized with FRET-based probes
Hisayoshi Yoshizaki,
Hisayoshi Yoshizaki
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
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Yusuke Ohba,
Yusuke Ohba
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
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Kazuo Kurokawa,
Kazuo Kurokawa
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
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Reina E. Itoh,
Reina E. Itoh
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
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Takeshi Nakamura,
Takeshi Nakamura
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
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Naoki Mochizuki,
Naoki Mochizuki
3Department of Structural Analysis, National Cardiovascular Center Research Institute, Osaka 565-8565, Japan
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Kazuo Nagashima,
Kazuo Nagashima
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
4Laboratory of Molecular and Cellular Pathology, Hokkaido University School of Medicine, Sapporo 060-8638, Japan
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Michiyuki Matsuda
Michiyuki Matsuda
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
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Hisayoshi Yoshizaki
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
Yusuke Ohba
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
Kazuo Kurokawa
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
Reina E. Itoh
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
Takeshi Nakamura
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
Naoki Mochizuki
3Department of Structural Analysis, National Cardiovascular Center Research Institute, Osaka 565-8565, Japan
Kazuo Nagashima
2Core Research for Evolutional Science and Technology, Japan Science and Technology Cooperation, Fukuoka 816-8580, Japan
4Laboratory of Molecular and Cellular Pathology, Hokkaido University School of Medicine, Sapporo 060-8638, Japan
Michiyuki Matsuda
1Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan
Address correspondence to M. Matsuda, Dept. of Tumor Virology, Institute for Microbial Diseases, Osaka University, Yamadaoka, Suita-shi, Osaka 565-0871, Japan. Tel.: 81-6-6879-8316. Fax: 81-6-6879-8314. E-mail: [email protected]
The online version of this article includes supplemental material.
*
Abbreviations used in this paper: FRET, fluorescence resonance energy transfer; GAP, GTPase-activating protein; GDI, guanine nucleotide dissociation inhibitor; GEF, guanine nucleotide exchange factor; RBD, RhoA-binding domain; TPEM, two-photon excitation fluorescence microscopy.
Received:
December 06 2002
Revision Received:
May 27 2003
Accepted:
May 29 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 162 (2): 223–232.
Article history
Received:
December 06 2002
Revision Received:
May 27 2003
Accepted:
May 29 2003
Citation
Hisayoshi Yoshizaki, Yusuke Ohba, Kazuo Kurokawa, Reina E. Itoh, Takeshi Nakamura, Naoki Mochizuki, Kazuo Nagashima, Michiyuki Matsuda; Activity of Rho-family GTPases during cell division as visualized with FRET-based probes . J Cell Biol 21 July 2003; 162 (2): 223–232. doi: https://doi.org/10.1083/jcb.200212049
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