CELL SPECIFIC HORMONAL REGULATION OF GENE EXPRESSION
Project Number3R01DK049698-04S1
Contact PI/Project LeaderSANDERS, MICHEL M
Awardee OrganizationUNIVERSITY OF MINNESOTA
Description
Abstract Text
Differential gene expression is the underlying determinant for cellular
diversity and differentiated cell function in complex organisms. Thus,
elucidation of the basis for cell-specific gene expression is required for
a molecular understanding of development and differentiation. The
activation and/or repression of specific genes is triggered by external
messages that act through signal transduction pathways that are largely
ubiquitous. An additional level of complexity exists for genes that are
regulated by hormones and growth factors; those genes can exhibit cell-
specificity for induced expression as well as for basal expression. The
long term goal of our research is to understand how hormonal,
developmental, and tissue-specific cues integrate to precisely control the
activities of complex genes. The focus of the research in this proposal is
to study cell-specific hormonal induction by identifying the cell-specific
elements in the chicken ovalbumin gene. This expression of this gene is
restricted to the tubular gland cells of the avian oviduct and is
regulated by four classes of steroid hormones and by the peptide hormone
insulin. The specific hypothesis being tested is that the cell-specific
expression of the ovalbumin gene is achieved via positive activation by
hormones in oviduct and direct repression by unknown factors in nonoviduct
tissues. The Specific Aims are to I). identify and characterize the
positive cell-specific regulatory elements in the ovalbumin gene, II).
clone the proteins that bind to the positive cell-specific elements, and
III). identify the elements in the ovalbumin gene that repress its
expression in inappropriate tissues. The identification and
characterization of the relevant DNA elements will be accomplished by
combination of in vivo footprinting, gel mobility shift assays, and gene
transfections. The cloning of the associated proteins will be attempted by
a one-hybrid yeast genetic selection system or by other techniques that
rely on the DNA binding properties of the proteins.
Elucidation of the underlying mechanisms involved in the generation and
maintenance of differentiated cells may provide the basis for
understanding how events go awry in some diseases such as cancer that
involve extensive alterations in cellular phenotype and proliferation.
Furthermore, the avian oviduct has the potential for producing large
amounts of easily purified proteins if expression can be targeted to that
organ. This has implications for research and for therapeutic and
commercial purposes.
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
847
DUNS Number
555917996
UEI
KABJZBBJ4B54
Project Start Date
25-June-1998
Project End Date
30-April-2000
Budget Start Date
25-June-1998
Budget End Date
30-April-2000
Project Funding Information for 1998
Total Funding
$4,350
Direct Costs
$2,959
Indirect Costs
$1,391
Year
Funding IC
FY Total Cost by IC
1998
National Institute of Diabetes and Digestive and Kidney Diseases
$4,350
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 3R01DK049698-04S1
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 3R01DK049698-04S1
Patents
No Patents information available for 3R01DK049698-04S1
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 3R01DK049698-04S1
Clinical Studies
No Clinical Studies information available for 3R01DK049698-04S1
News and More
Related News Releases
No news release information available for 3R01DK049698-04S1
History
No Historical information available for 3R01DK049698-04S1
Similar Projects
No Similar Projects information available for 3R01DK049698-04S1