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Faculty Detail    
Name PETER J DETLOFF
 
Campus Address KAUL 540B Zip 0024
Phone 205-975-8157
E-mail detloff@uab.edu
Other websites
     


Faculty Appointment(s)
Appointment Type Department Division Rank
Primary  Biochemistry & Molecular Genetics  Biochemistry & Molecular Genetics Associate Professor
Secondary  Neurobiology  Neurobiology Assistant Professor
Center  Center for Biophysical Sciences/Engineering  Center for Biophysical Sciences/Engineering Associate Professor
Center  Civitan International Research Center  Civitan International Research Center Associate Professor
Center  Comprehensive Cancer Center  Comprehensive Cancer Center Associate Professor
Center  General Clinical Research Center  Comprehensive Neuroscience Center Associate Professor
Center  Neurology   Ctr Neurodegeneration & Exp Ther (CNET) Associate Professor

Graduate Biomedical Sciences Affiliations
Biochemistry and Molecular Genetics Program 
Cellular and Molecular Biology Program 
Genetics and Genomic Sciences 
Neuroscience 
Neurosciences 
Pathobiology and Molecular Medicine 

Biographical Sketch 
Peter J. Detloff (b. 1963) received his B.S. degree in Biochemistry from the University of Illinois at Champaign Urbana in 1985 and his Ph.D. degree from the University of Chicago in 1991. He was a postdoctoral fellow with Professor Oliver Smithies in the Department of Pathology in the School of Medicinie at the University of North Carolina at Chapel Hill. In 1993 he joined UAB as an Assistant Professor in the Department of Biochemistry and Molecular Genetics.

Research/Clinical Interest
Title
Mouse Models of Human Genetic Disorders
Description
The combination of gene targeting and embryonic stem (ES) cell technologies allows the introduction of precise alterations into the mouse germline. Gene targeting involves the alteration of a gene in cultured cells by homologous recombination between the endogenous gene and a modified clone of the gene. The modified cells are then introduced into a murine embryo and contribute to the tissues of the developing mouse. The modification may be transmitted to progeny to create a strain of mice harboring a desired genetic alteration. My work has focused on improving methods of gene targeting. Prior to coming to UAB, I developed a method of repeatedly targeting genes in ES cells. The method allowed me to replace the ß-globins expressed in adult mouse with the human ß-globin allele responsible for sickle cell anemia. My laboratory will use ES cell technology to study human disorders associated with the expansion of nucleotide repeats. Huntington’s disease (HD), an example of one of these diseases, is an autosomal dominant disorder causing irreversible neural degeneration. Recently, the gene responsible for HD was cloned. Affected individuals differ from normal by having a greater number of CAG repeats near the beginning of this gene. Onset of the disease usually occurs after reproductive age (30-60 yrs.) and the age of onset may be inversely related to the number of repeats. The biochemical function of the disease gene, the pathology of the disease at the molecular level, and the mechanism by which the repeats expand is not yet known. We will use culture systems and mouse models to investigate the mechanism of repeat expansion as well as the pathological consequences of these expansions. These experiments may reveal important information regarding the increasing number of diseases associated with repeat expansion, including: fragile X- syndrome, myotonic dystrophy, and spinobulbar muscular atrophy.

Selected Publications 
Publication PUBMEDID
Jackson WS, Tallaksen-Greene SJ, Albin RL, Detloff PJ. Nucleocytoplasmic transport signals affect the age at onset of abnormalities in knock-in mice expressing polyglutamine within an ectopic protein context. Hum Mol Genet. 2003 Jul 1;12(13):1621-9.    
Dixon KT, Cearley JA, Hunter JM, Detloff PJ. Mouse Huntington's disease homolog mRNA levels: variation and allele effects. Gene Expr. 2004;11(5-6):221-31.    
Choo YS, Johnson GV, MacDonald M, Detloff PJ, Lesort M. Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release. Hum Mol Genet. 2004 Jul 15;13(14):1407-20. Epub 2004 May 26.    
Crouse AB, Detloff PJ. Allele-specific conditional destabilization of glutamine repeat mRNAs. Gene Expr. 2005;12(3):213-22.    
Hunter JM, Crouse AB, Lesort M, Johnson GV, Detloff PJ. Verification of somatic CAG repeat expansion by pre-PCR fractionation. J Neurosci Methods. 2005 May 15;144(1):11-7. Epub 2004 Nov 28.