How cells acquire different determined states is the fundamental question in developmental biology. Cells are determined if they develop after transplantation according to information from their original location. Transdetermination is the phenomenon whereby determined cells alter their original fate to a new, completely different fate. The archetypal transdetermination occurs in imaginal discs, the precursors of appendages of Drosophila melanogaster, after fragmentation and prolonged periods of growth. Virtually nothing in known about the molecular basis of transdetermination. Our lab has recently made the observation that transdetermination is induced without imaginal disc fragmentation by expressing the segment polarity gene, wingless, ectopically in cell clones of pro thoracic leg imaginal discs of Drosophila (Maves and Schubiger, submitted for publication). The overall objective of this proposal is to identify other genes that cause transdetermination after ectopic expression in imaginal discs, and to group them into a functional hierarchy. For these experiments the flp-out system will be used. These experiments will lead to the creation of an inventory of transdetermination events caused by ectopic wingless expression, identification of genes in the pathway leading to transdetermination by analysis of changes in gene expression provoked by ectopic wingless expression, and determination of whether genes whose expression is altered can also induce transdetermination. Transdetermination has obvious parallels with tumorigenesis. Like transdetermination, cancer cells depart from their ancestral paths and enter new developmental pathways. In both, the new cell types result from new gene activities that are inherited in their progeny, and new patterns of growth are involved. The proposed research will lead to an understanding of how these processes occur, and will add to our understanding of the more basic question of how cells acquire different states of determination. It is hoped that ultimately this work will contribute to the understanding, prevention and treatment of tumors.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM017373-04
Application #
2456230
Study Section
Special Emphasis Panel (ZRG2-BIOL-1 (01))
Project Start
1997-03-01
Project End
Budget Start
1997-03-01
Budget End
1998-02-28
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
075524595
City
Seattle
State
WA
Country
United States
Zip Code
98109
Johnston, L A; Ostrow, B D; Jasoni, C et al. (1998) The homeobox gene cut interacts genetically with the homeotic genes proboscipedia and Antennapedia. Genetics 149:131-42
Neufeld, T P; de la Cruz, A F; Johnston, L A et al. (1998) Coordination of growth and cell division in the Drosophila wing. Cell 93:1183-93
Johnston, L A; Schubiger, G (1996) Ectopic expression of wingless in imaginal discs interferes with decapentaplegic expression and alters cell determination. Development 122:3519-29