The major objective of the proposed research is to introduce a new gene into one or more large animal species and to study the effects of the foreign gene. Studies with mice have demonstrated the usefulness of the gene transfer technique to study gene regulation and development. However, the transfer of new genes into large animals will allow several types of investigations not readily undertaken in mice. There are two major specific aims: (1) To introduce a functional metallothionein-growth hormone gene into a large animal such as a rabbit, sheep, goat, pig or cow. This gene construction functions well in mice and would provide and opportunity to extend the gene transfer system to large animals. In addition, studies on the effect of the new gene on several aspects of growth, lactation, and endocrine balance would be facilitated in large animals. (2) To introduce a functional human blood clotting factor IX gene into a large animal. The presence of a functioning factor IX gene in various tissues of several species will allow us to examine the effect of tissue type and species on critical biochemical reactions, such as Gamma-carboxylation and glycosylation, that are important in processing protein. Large animals are required to provide the substantial amounts of tissue needed for the protein processing assays. Since transgenic animals should synthesize an identical protein in several tissues of a species and also in the different species, these animals will provide a unique opportunity to study the role of tissue factors in protein processing.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD019018-03
Application #
3316179
Study Section
Reproductive Biology Study Section (REB)
Project Start
1984-07-01
Project End
1987-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
Schools of Veterinary Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Theisen, M; Behringer, R R; Cadd, G G et al. (1993) A C/EBP-binding site in the transferrin promoter is essential for expression in the liver but not the brain of transgenic mice. Mol Cell Biol 13:7666-76
Rexroad Jr, C E; Mayo, K; Bolt, D J et al. (1991) Transferrin- and albumin-directed expression of growth-related peptides in transgenic sheep. J Anim Sci 69:2995-3004
Palmiter, R D; Sandgren, E P; Avarbock, M R et al. (1991) Heterologous introns can enhance expression of transgenes in mice. Proc Natl Acad Sci U S A 88:478-82
Lo, D; Pursel, V; Linton, P J et al. (1991) Expression of mouse IgA by transgenic mice, pigs and sheep. Eur J Immunol 21:1001-6
Guthrie, H D; Pursel, V G; Miller, K F et al. (1991) Effect of bovine growth hormone gene expression, sex and age on plasma gonadotropins, estrone and testosterone in prepuberal pigs. Domest Anim Endocrinol 8:423-9
Doi, T; Striker, L J; Gibson, C C et al. (1990) Glomerular lesions in mice transgenic for growth hormone and insulinlike growth factor-I. I. Relationship between increased glomerular size and mesangial sclerosis. Am J Pathol 137:541-52
Frohman, L A; Downs, T R; Kashio, Y et al. (1990) Tissue distribution and molecular heterogeneity of human growth hormone-releasing factor in the transgenic mouse. Endocrinology 127:2149-56
Pursel, V G; Bolt, D J; Miller, K F et al. (1990) Expression and performance in transgenic pigs. J Reprod Fertil Suppl 40:235-45
Pursel, V G; Hammer, R E; Bolt, D J et al. (1990) Integration, expression and germ-line transmission of growth-related genes in pigs. J Reprod Fertil Suppl 41:77-87
Habener, J F; Cwikel, B J; Hermann, H et al. (1989) Metallothionein-vasopressin fusion gene expression in transgenic mice. Nephrogenic diabetes insipidus and brain transcripts localized to magnocellular neurons. J Biol Chem 264:18844-52

Showing the most recent 10 out of 24 publications