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Activity of Rho-family GTPases during cell division as visualized with FRET-based probes
Authors:Yoshizaki Hisayoshi  Ohba Yusuke  Kurokawa Kazuo  Itoh Reina E  Nakamura Takeshi  Mochizuki Naoki  Nagashima Kazuo  Matsuda Michiyuki
Affiliation:Department of Tumor Virology, Research Institute for Microbial Diseases, Osaka University, Japan.
Abstract: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.
Keywords:fluorescent probes   cytokinesis   rho GTP-binding proteins   rac GTP-binding proteins   Cdc42 GTP-binding protein
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