Steve Kron, M.D., Ph.D.


Primary:

Associate Professor, Molecular Genetics and Cell Biology


Secondary:

Committee on Genetics
Committee on Cancer Biology
Committee on Cellular and Molecular Physiology
Committee on Molecular Medicine
Committee on Molecular Medicine and The College


Education:

Degree Year Institution Area
BA

1982

University of Pennsylvania               
Biochemistry
MSE
1983

University of Pennsylvania 

Bioengineering
MD
1990
 
Stanford University
Medicine
PhD

1990

Stanford University

Cell Biology



Phone: (773) 834-0250  /  Fax: (773) 702-4394  /  Lab:  (773) 834-0256
E-Mail: skron@uchicago.edu
Address: 924 E. 57th Street
Chicago, IL 60637
JFK R320
Lab: JFK R322

Web page:
http://mgcb.bsd.uchicago.edu/
http://mgcb.bsd.uchicago.edu/faculty/kron/index.html


Research Summary

DNA damage responses; Phosphoproteomics in cell signaling, diagnostics and drug discovery.

The Kron laboratory is a highly collaborative group of cell biologists, geneticists, biochemists and chemists. Our major basic research efforts are directed at 1) dissecting cyclin dependent kinase structure and function in yeast, 2) defining roles for chromatin modifications in DNA damage response, and 3) developing novel mass spectrometry methods for phosphoproteomics and high throughput screening. We also pursue translational projects directed at 1) developing Bcr-Abl assays for diagnostics and antagonists for therapeutics and 2) discovering inhibitors of cellular response to DNA double strand breaks as an approach to radiosensitization.


Selected Publications

Wu, D., Nair-Gill, E., Sher, D.A., Parker, L.L., Campbell, J.M., Siddiqui, M., Stock, W. and Kron, S.J. Assaying Bcr-Abl kinase activity and inhibition in whole cell extracts by phosphorylation of substrates immobilized on agarose beads. Anal. Biochem., 347:67-76, 2005.   PubMed Citation

Parker, L.L., Schilling, A.B., Kron, S.J. and Kent, S.B.  Optimizing thiophosphorylation in the presence of competing phosphorylation with MALDI-TOF-MS detection. J. Proteome Res., 4:1863-66, 2005.   PubMed Citation

Wysocki, R., Javaheri, A., Allard, S., Sha, F., Cote, J. and Kron, S.J. (2005). Role of Dot1-dependent histone H3 methylation in G1 and S phase DNA damage checkpoint functions of Rad9. Mol. Cell. Biol., 25:8430-43. PubMed Citation

Parker, L. L., Kurutz, J. W., Kent, S. B. and Kron, S.J. Control of the yeast cell cycle with a photocleavable alpha-factor analogue. Angew Chem. Int. Ed. Engl., 45:6322-5, 2006.  PubMed Citation

Javaheri, A., Wysocki, R., Jobin-Robitaille, O., Altaf, M., Cote, J. and Kron, S.J. Yeast G1 DNA damage checkpoint regulation by H2A phosphorylation is independent of chromatin remodeling. Proc. Natl. Acad. Sci. U.S.A., 103:13771-6, 2006.   PubMed Citation

Wysocki, R., Javaheri, A., Kristjansdottir, K., Sha, F. and Kron, S.J.  CDK Pho85 targets CDK inhibitor Sic1 to relieve yeast G1 checkpoint arrest after DNA damage.  Nat. Struct. Mol. Biol., 13:908-914, 2006. PubMed Citation

Updated 9/21/07.