Mol. Cells 2009; 27(3): 345-350
Published online March 19, 2009
https://doi.org/10.1007/s10059-009-0044-9
© The Korean Society for Molecular and Cellular Biology
We previously reported that flavone induces embryonic lethality in Caenorhabditis elegans, which appeared to be the result of cell cycle arrest during early embryogenesis. To test this possibility, here we examined whether flavone inhibits the activity of a key cell cycle regulator, CDC-25.1 in C. elegans. A gain-of-function cdc-25.1 mutant, rr31, which exhibits extra cell divisions in intestinal cells, was used to test the inhibitory effects of flavone on CDC-25 activity. Flavone inhibited the extra cell divisions of intestinal cells in rr31, and modifications of flavone reduced the inhibitory effects. The inhibitory effects of flavone on CDC-25.1 were partly, if not completely, due to transcriptional repression.
Keywords Caenorhabditis elegans, CDC-25 phosphatase inhibitor, flavone (2-phenyl chromone), hyperplasia, intestinal cell division
Mol. Cells 2009; 27(3): 345-350
Published online March 31, 2009 https://doi.org/10.1007/s10059-009-0044-9
Copyright © The Korean Society for Molecular and Cellular Biology.
Koo-Seul Kim, Ichiro Kawasaki, Youhoon Chong, and Yhong-Hee Shim
We previously reported that flavone induces embryonic lethality in Caenorhabditis elegans, which appeared to be the result of cell cycle arrest during early embryogenesis. To test this possibility, here we examined whether flavone inhibits the activity of a key cell cycle regulator, CDC-25.1 in C. elegans. A gain-of-function cdc-25.1 mutant, rr31, which exhibits extra cell divisions in intestinal cells, was used to test the inhibitory effects of flavone on CDC-25 activity. Flavone inhibited the extra cell divisions of intestinal cells in rr31, and modifications of flavone reduced the inhibitory effects. The inhibitory effects of flavone on CDC-25.1 were partly, if not completely, due to transcriptional repression.
Keywords: Caenorhabditis elegans, CDC-25 phosphatase inhibitor, flavone (2-phenyl chromone), hyperplasia, intestinal cell division
Ichiro Kawasaki*, Myung-Hwan Jeong, and Yhong-Hee Shim*
Mol. Cells 2011; 31(2): 191-197 https://doi.org/10.1007/s10059-011-0021-ySunny Ko, Jae-Hyung Park, Ah-Reum Lee, Eugene Kim, Jiyoung-Kim, Ichiro Kawasaki, and Yhong-Hee Shim*
Mol. Cells 2010; 30(2): 167-172 https://doi.org/10.1007/s10059-010-0103-2Jiyoung Kim, Ah-Reum Lee, Ichiro Kawasaki, Susan Strome, and Yhong-Hee Shim
Mol. Cells 2009; 28(1): 43-48 https://doi.org/10.1007/s10059-009-0098-8