Research: Transcriptional regulatory proteins function as repressors or activators of gene expression and play a paramount role in cellular differentiation. The overall goal of this proposal is to increase our understanding of transcriptional regulatory mechanisms that govern differentiation of cardiac and skeletal myocytes. The winged helix or forkhead/HNF-3 gene family is comprised of several recently identified proteins that function in pattern formation in the early embryo. Preliminary studies in this laboratory have identified a novel member of the winged helix family that is expressed in cardiac and skeletal muscle, termed myocyte nuclear factor (MNF). MNF exhibits sequence-specific DNA binding to a positive transcriptional control element within a muscle- specific enhancer region from the human myoglobin gene. The major hypothesis to be addressed by this grant proposal is that MNF and/or closely related winged helix proteins play a significant role in differentiation of skeletal and cardiac myocytes. The following four specific aims are proposed: l) to clone the mouse genomic locus encoding MNF; 2) to identify and to define the relationships between members of the winged helix gene family that are expressed in cardiac and skeletal muscle (i.e. variants generated by alternative splicing); 3) to examine the spatial and temporal distribution of MNF during embryogenesis; 4) to determine the functional importance of winged helix proteins during development by gene disruption using homologous recombination in embryonic stem cells and subsequent generation of strains of mice bearing homozygous null mutations in the gene(s) encoding these proteins. Achievement of these aims will define the role of MNF in cardiac and skeletal myogenesis. In the long term, advances in our understanding of the control of muscle development may foster novel strategies to improve cardiac function in patients with cardiovascular disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HL003231-02
Application #
2853105
Study Section
Research Training Review Committee (RTR)
Project Start
1995-08-01
Project End
2000-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Yang, Q; Kong, Y; Rothermel, B et al. (2000) The winged-helix/forkhead protein myocyte nuclear factor beta (MNF-beta) forms a co-repressor complex with mammalian sin3B. Biochem J 345 Pt 2:335-43
Garry, D J; Yang, Q; Bassel-Duby, R et al. (1997) Persistent expression of MNF identifies myogenic stem cells in postnatal muscles. Dev Biol 188:280-94