desciption): The Myc family proteins play fundamental roles in controlling cell proliferation, and frequently contribute to oncogenesis. The biological activities of Myc proteins require heterodimerization with Max, which functions as an obligate partner for DNA-binding and transcriptional activities. Max fulfills a similar role in mediating the transcriptional and biological activities of the Myc-related proteins Mad 1-4, Mnt, and Mga. Thus, Myc proteins are thought to function as a network of Max-interacting proteins that regulate overlapping sets of target genes and biological processes. This project aims to understand the molecular and biological functions of the Mga protein and how these impinge on Myc function. The Mga protein contains a Myc-like basic-helix-loop-helix-leucine zipper (bHLHZip) domain and interacts with Max, and is of particular interest because it contains a second highly conserved DNA-binding domain called the T-domain. Proteins with a T-domain motif, such as Brachyury, regulate inductive events that govern formation of many organs and appendages during embryonic development and are implicated in various human birth defects. Mutagenesis and transcription assays will be used to test the hypothesis that Mga functions as a dual-specificity transcription factor that regulates both Myc:Max and Brachyury target genes. The potential regulatory roles imparted by Mga-interacting proteins, including a putative corepressor, will also be investigated. Finally, gene targeting in the mouse will be used to study the biological activities of Mga and the individual roles of its bHLHZip domain and T-domain.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA087788-04
Application #
6633808
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Perry, Mary Ellen
Project Start
2000-07-01
Project End
2005-06-30
Budget Start
2003-07-01
Budget End
2005-06-30
Support Year
4
Fiscal Year
2003
Total Cost
$271,800
Indirect Cost
Name
Oregon Health and Science University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Walker, William; Zhou, Zi-Qiang; Ota, Sara et al. (2005) Mnt-Max to Myc-Max complex switching regulates cell cycle entry. J Cell Biol 169:405-13
Toyo-oka, Kazuhito; Hirotsune, Shinji; Gambello, Michael J et al. (2004) Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller-Dieker syndrome. Hum Mol Genet 13:1057-67