Work in this group focuses on the elucidation of the developmental signals that are required to regulate cell proliferation. To this end, we have been studying a gene, roughex (rux), that is required to arrest cells in G1 in the developing compound eye of Drosophila. Genetic and biochemical interactions suggest that rux is acting as a novel type of cyclin kinase inhibitor, a class of proteins recently identified in both yeast and mammalian systems. We have recently shown that overexpression of Rux in vivo inhibits mitosis and leads to endoreduplication, phenotypes also observed in mutations of the G2 Cyclin A (CycA). Mutations in rux interact genetically with CycA, in that loss-of- function mutations in CycA act as dominant suppressers of the rux phenotype. In addition, overexpression of CycA phenocopies rux, and co- expression of Rux reverses this. Finally, overexpression of Rux blocks mitosis by inhibiting accumulation or by stimulating destruction of the G2 cyclins CycA and CycB and mislocalizing cycA to the nucleus. Rux itself is expressed in a dynamic pattern in the developing eye. Expression begins in a band anterior to the morphogenetic furrow (MF) corresponding to the G1 domain that is absent in the mutant. Expression is decreased in the MF, and then Rux protein is seen to reaccumulate behind the MF and is rapidly down-regulated in cells that re-enter S phase in this region. Down-regulation of Rux protein is comcomitant with CycE expression in these cells; ectopic overexpression of CycE in cells constitutively expressing Rux behind the furrow leads to destabilization of Rux protein and re-accumulation of cyclins A and B. We propose a model whereby Rux is required to inhibit Cyclin A activity in G1, possibly by targeting CycA for destruction. As cells enter S phase, they are inactivated by a CycE-dependent mechanism, releasing CycA for its mitotic role.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC005275-03
Application #
6100792
Study Section
Special Emphasis Panel (LB)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
National Cancer Institute Division of Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Avedisov, S N; Krasnoselskaya, I; Mortin, M et al. (2000) Roughex mediates G(1) arrest through a physical association with cyclin A. Mol Cell Biol 20:8220-9