Rubinstein-Taybi syndrome is a genetic syndrome characterized by facial abnormalities, broad thumbs, broad toes, mental retardation and other abnormalities. It is due to mutations in the gene encoding CREB Binding Protein (CBP), although the link between the mutations and the clinical phenotype is not understood. CBP is a protein that is thought to play a critical role in thyroid hormone action--it is a co-activator protein that forms a bridge between the thyroid hormone receptor and the transcription machinery, thus transmitting the signal from thyroid hormone (T3) to allow regulation of gene expression. The CBP mutations that encompass Rubinstein-Taybi syndrome are diverse, and hence there is genetic heterogeneity in this condition. The hypothesis to be tested is that at least some of these CBP mutations disrupt the ability of CBP to function as a T3 receptor co-activator, resulting in a state of thyroid hormone resistance.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000042-39S1
Application #
6113520
Study Section
Project Start
Project End
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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