The application is for the continued support of a Program Project Grant in one of the NICHD-funded Mental Retardation Research Centers. The program comprises five projects whose goal is better understanding of the biochemical defects and/or pathogenesis of a number of inborn errors which can result in mental retardation and/or early death. Conditions to be studied are glutaric acidemia types I and II, homocystinuria due to cystathionine beta-synthase deficiency and various defects of the mitochondrial respiratory chain. Drs. Goodman, Frerman and Kraus, the three BF Stolinsky Laboratories investigators, have common interests and goals, interact on a daily basis, use the same methods and equipment, and utilize common tissue culture and recombinant DNA cores of the MRRC. Dr. Neil Howell, at the University of Texas in Galveston, has been collaborating with us for several years, and brings longstanding expertise and interest in the biochemistry and molecular biology of the respiratory chain to the project. Project I is concerned with glutaric acidemia, a disorder which causes mental retardation and degeneration of the basal ganglia, and will examine functional domains of normal glutaryl-coenzyme A dehydrogenase as well as how normal function is perturbed by naturally occurring mutations. Projects II and IV focus on the biochemistry and molecular biology of glutaric acidemia type II (GA2), a disorder which causes early death and (often) congenital anomalies, examining the effect of mutations of two proteins (ETF and ETF:QO) whose deficiency causes it. Project III seeks to identify mutations of the mitochondrial genome in patients with Leber's Hereditary Optic Neuropathy (LHON) and selected neuromuscular disorders; and project V will examine genetic heterogeneity in patients with propionic acidemia and homocystinuria due to deficiency of cystathionine beta-synthase. All of these projects have the common goal of eventually understanding how disturbed enzyme function leads to disease, since such information is essential for formulating rational approaches to therapy.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
2P01HD008315-16
Application #
3096602
Study Section
Special Emphasis Panel (SRC (SG))
Project Start
1979-04-01
Project End
1994-06-30
Budget Start
1991-07-01
Budget End
1992-06-30
Support Year
16
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
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Chloupkova, M; Ravn, K; Schwartz, M et al. (2000) Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coli. Mol Genet Metab 71:623-32
Maclean, K N; Janosik, M; Oliveriusova, J et al. (2000) Transsulfuration in Saccharomyces cerevisiae is not dependent on heme: purification and characterization of recombinant yeast cystathionine beta-synthase. J Inorg Biochem 81:161-71

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