Drosophila myb is required for the G2/M transition and maintenance of diploidy

被引:67
作者
Katzen, AL [1 ]
Jackson, J
Harmon, BP
Fung, SM
Ramsay, G
Bishop, JM
机构
[1] Univ Illinois, Dept Mol Genet, Coll Med, Chicago, IL 60607 USA
[2] Univ Calif San Francisco, George Williams Hooper Fdn, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
cell cycle; transcription factor; proto-oncogene; G(2)/M; endoreduplication; diploidy;
D O I
10.1101/gad.12.6.831
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The myb proto-oncogenes are thought to have a role in the cell division cycle. We have examined this possibility by genetic analysis in Drosophila melanogaster, which possesses a single myb gene. We have described previously two temperature-sensitive, recessive lethal mutants in Drosophila myb (Dm myb). The phenotypes of these mutants revealed a requirement for myb in diverse cellular lineages throughout the course of Drosophila development. We now report a cellular explanation for these findings by showing that Dm myb is required for both mitosis and prevention of endoreduplication in wing cells. Myb apparently acts at or near the time of the G(2)/M transition. The two mutant alleles of Dm myb produce the same cellular phenotype, although the responsible mutations are located in different functional domains of the gene product. The mutant phenotype can be partially suppressed by ectopic expression of either cdc2 or string, two genes that are known to promote the transition from G(2) to M. We conclude that Dm myb is required for completion of cell division and may serve two independent functions: promotion of mitosis, on the one hand, and prevention of endoreduplication when cells are arrested in G(2), on the other.
引用
收藏
页码:831 / 843
页数:13
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