The long-term goals are to understand how positional identity of skeletal muscles is established, and specifically, how jaw muscles are specified and maintained. The homeogene Engrailed-2 (En-2) has been shown to be differentially expressed in a subset of jaw muscles (masseter, temporalis). It is first detected in early myogenic founder cells in the first arch, suggesting a role in establishment and development of these muscles. The continued expression of En-2 in adults suggests that it may also play a role in maintenance of mature muscle phenotype. In order to determine the role of En-2 in jaw muscle development, the PI proposes to examine loss-of-function, using En-2 -/- knockouts, and gain of function using En-2 placed under the control of characterized muscle regulatory elements in transient and stable transgenic animals. In order to learn about jaw-specific regulation of En-2, the PI proposes to molecularly dissect the En-2 enhancer with reporter gene constructs in mouse transgenic founders or lines, and to determine the human regulatory elements to aid in identifying conserved sites underlying jaw-specific En-2 expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE011953-03
Application #
2749360
Study Section
Special Emphasis Panel (ZDE1-GH (11))
Project Start
1996-09-15
Project End
2000-07-14
Budget Start
1998-07-15
Budget End
1999-07-14
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Biochemistry
Type
Schools of Medicine
DUNS #
114400633
City
New York
State
NY
Country
United States
Zip Code
10029
Degenhardt, Karl; Rentschler, Stacey; Fishman, Glenn et al. (2002) Cellular and cis-regulation of En-2 expression in the mandibular arch. Mech Dev 111:125-36
Degenhardt, K; Sassoon, D A (2001) A role for Engrailed-2 in determination of skeletal muscle physiologic properties. Dev Biol 231:175-89
Miller, C; Degenhardt, K; Sassoon, D A (1998) Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis. Nat Genet 20:228-30