There are over 35 mouse homeobox-containing genes known as Hox. The Hox genes are divided into four multigene dusters (Hox-A, -B, -C, & -D), which reside on four different chromosomes. These genes are expressed in restricted patterns during embryogenesis. The function of Hox genes during mammalian development was first studied by overexpressing the Hoxa-4 gene in transgenic mice (Wolgemuth et al., 1989). That study demonstrated for the first time that the expression of a mammalian homeobox-containing gene could alter development. Since then, studies using gain of function and loss of function transgenic mice have suggested that the Hox genes constitute a complex genetic network for patterning the mouse embryo. In this application, experiments are proposed to study the individual and combined roles of a specific class of Hox genes during mouse development. This class of mouse Hox genes is known as the Deformed class or Group 4, which includes the four Hox genes Hoxa-4, b-4, c-4, and d-4. These Hox genes possess a homeodomain most similar to Drosophila Deformed and constitute a paralogous group of genes between the clusters. Gene targeting experiments have been initiated using mouse embryonic stem (ES) cells to generate Hoxa-4, c-4, and d-4 mutations in the germ line of mice to study their required functions during mammalian development. Germ line chimeras derived from Hoxa-4 mutant ES cells have already been generated. In addition to the individual Hox phenotypes, mice carrying these three Hox mutations and the recently reported Hoxb-4 mutation (Ramirez-Solis et al., 1993) will be interbred to produce mice deficient for two or more of these genes. The production of mouse strains that possess the four Deformed-class Hox gene mutations will provide a powerful resource for studying the function of Hox genes. These focused studies should provide important information about the roles of a specific class of Hox genes during mouse development. The information gained in this model system should be useful in understanding normal and abnormal human development.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD031568-01
Application #
2204178
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Project Start
1994-05-01
Project End
1998-04-30
Budget Start
1994-05-01
Budget End
1995-04-30
Support Year
1
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Genetics
Type
Other Domestic Higher Education
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Zhang, W; Behringer, R R; Olson, E N (1995) Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies. Genes Dev 9:1388-99
Horan, G S; Ramirez-Solis, R; Featherstone, M S et al. (1995) Compound mutants for the paralogous hoxa-4, hoxb-4, and hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed. Genes Dev 9:1667-77
Horan, G S; Wu, K; Wolgemuth, D J et al. (1994) Homeotic transformation of cervical vertebrae in Hoxa-4 mutant mice. Proc Natl Acad Sci U S A 91:12644-8
Rosati, R; Horan, G S; Pinero, G J et al. (1994) Normal long bone growth and development in type X collagen-null mice. Nat Genet 8:129-35