The goal is to improve the performance of the DNA-affinity chromatography of transcription factors and to increase understanding of genetic regulation. Many of the transcription factors (TFs;e.g., c- jun, c-myc) were originally discovered as oncogenes and genetic regulation is important to the understanding of genetic disease. The relevance to human health and well-being is clear. We will: 1. Develop a novel and innovative method for characterizing promoters. The way promoter structure is now studied is to identify each response element contained within its sequence, use the electrophoretic mobility shift assay to detect whether the isolated element is in fact bound by a nuclear protein, and then use DNA-affinity chromatography and other methods to purify the proteins, one-at-a-time. For complex promoters, this linear approach is tedious and prolonged. Promoter Trapping was developed in the last funding period and has the potential to provide a completely novel way to characterize a promoter;mapping and identification of all transcription factors that bind in a few steps using gel blots. We have recently combined 2DGE with southwestern blotting and on- blot digestion to allow the sensitive detection of TFS and allow mass spectrometry characterization directly from the blot. Combined with promoter trapping, these promoter complexes can likely be analyzed from a few gel blots. We will determine if this new approach can speed research progress. 2. Novel 3-dimensional gel electrophoresis (3DGE) methods will be developed to solve intractable TFs. Three new 3DGE methods will be developed to further separate the proteins obtained from systematic oligonucleotide trapping (SOT) and promoter trapping (PT). The first dimension in each case relies on specific DNA binding electrophoresis, then a second and third dimension of pI and SDS-PAGE. These new techniques will resolve any intractable transcription factor identifications. 3. Alternative trapping methods will solve problems with current trapping technology. SOT has been proven to be the most powerful techniques available for purifying transcription factors but it is not perfect. The ends of the oligonuleotide used for trapping are binding DNA repair proteins as contaminants which can obscure identification. We will develop alternatives which use either thiol-disulfide chemistry or alternatively, immobilized metal affinity chromatography, to solve this problem. The result of the proposed studies will be truly innovative and transformative ways to study genetic regulation. These experiments will require four years.

Public Health Relevance

Many oncogenes are transcription factors, showing the relevance of transcription factors to cancer and also the importance of transcription factors to cell division and other biological processes. To understand genetic disease and genetic regulation, the function of transcription factors must also be understood. Here, we improve the purification and characterization of these important proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM043609-24
Application #
8499322
Study Section
Enabling Bioanalytical and Biophysical Technologies Study Section (EBT)
Program Officer
Edmonds, Charles G
Project Start
1989-08-01
Project End
2014-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
24
Fiscal Year
2013
Total Cost
$287,045
Indirect Cost
$86,421
Name
University of Texas Health Science Center San Antonio
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
800189185
City
San Antonio
State
TX
Country
United States
Zip Code
78249
Nagore, Linda I; Jarrett, Harry W (2015) T(3): targeted proteomics of DNA-binding proteins. Anal Biochem 474:8-15
Jia, Yinshan; Jarrett, Harry W (2015) Method for trapping affinity chromatography of transcription factors using aldehyde-hydrazide coupling to agarose. Anal Biochem 482:1-6
Jia, Yinshan; Nagore, Linda; Jarrett, Harry (2015) Southwestern Blotting Assay. Methods Mol Biol 1334:85-99
Jia, Yinshan; Larionov, Oleg; Jarrett, Harry W (2014) Coupling of deoxyribonucleic acid to solid supports using 3' terminal ribose incorporation. J Chromatogr A 1339:73-9
Hoffmann, Christoph; Zimmermann, Anika; Hinney, Anke et al. (2013) A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytes. PLoS One 8:e83426
Nagore, L I; Nadeau, R J; Guo, Q et al. (2013) Purification and characterization of transcription factors. Mass Spectrom Rev 32:386-98
Jarrett, Harry W (2012) Proteomic methodologies to study transcription factor function. Methods Mol Biol 786:315-34
Zhou, Yanwen; Jia, Yinshan; Jarrett, Harry W (2012) Asymmetric polymerase chain reaction provides alternatives for preparation of (GT)ýýý-tailed duplex DNA promoter for promoter trapping. Anal Biochem 427:133-8
Jiang, Daifeng; Mummidi, Srinivas; Ahuja, Sunil K et al. (2011) CCR5 promoter haplotype transcription complex characterization. J Health Care Poor Underserved 22:73-90
Jiang, Daifeng; Jia, Yinshan; Jarrett, Harry W (2011) Transcription factor proteomics: identification by a novel gel mobility shift-three-dimensional electrophoresis method coupled with southwestern blot and high-performance liquid chromatography-electrospray-mass spectrometry analysis. J Chromatogr A 1218:7003-15

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