Biology4
Douglas Bernstein

Douglas Bernstein

Assistant Professor

|
CL 231B  Phone: 765-285-8851  

Department of Biology
Ball State University
Cooper Life Science Building, CL 121
Muncie, IN 47306

Education and Training:

Whitehead Institute for Biomedical Research, Cambridge, MA
Postdoctoral Fellow 2007-2015

University of Wisconsin, Madison, Madison, WI
Ph.D. Biomolecular Chemistry 2001-2006 

Rutgers University, New Brunswick, New Brunswick, NJ
B.S. Biochemistry 1997-2001Bernstein Graphic 1

Research Interests:

My general interests are in RNA processing and modification.

Specific Goal:  We investigate pseudouridylation in the human fungal pathogen C. albicans.

  • Molecular biology and biochemistry
  • Medical mycology
  • RNA processing and metabolism
  • Genetics

A principle reason for the absence of more effective antifungal therapeutics is that we do not have sufficient knowledge about the basic biology of fungi, and what distinguishes them from humans at the molecular level. My lab’s research has identified several fundamental aspects of RNA metabolism that distinguish fungi from humans. Bernstein Graphic 2We leverage a broad range of biological, biochemical, and biophysical tools to characterize clinically relevant features of fungal RNA metabolism in the human pathogen C. albicans. Our work aims to advance our understanding of RNA processing variation, and has the potential to lead to the discovery of novel antifungal compounds.

Select Publications:

Bernstein D.A.*, Schwartz S.*, Mumbach M.R.*, Jovanovic M., Herbst R.H., León-Ricardo B.X, Engreitz J.M., Guttman M., Satija R., Lander E.S., Fink G.R., Regev A. (2014) “ Transcriptome wide mapping reveals widespread dynamic pseudouridylation of ncRNA and mRNAs” CELL 159 (1): 148–162. 

Bernstein D.A.*, Marceau A. H.*, Walsh B.W., Shapiro W., Simmons L.A., Keck J.L. (2013) “Protein interactions in genome maintenance as novel antimicrobial targets” PLOS1 ;8(3).

Bernstein D.A., Vyas V.K., Fink G.R. Commentary on “Candida albicans Dicer (Dcr1) is required for efficient ribosomal and spliceosomal RNA maturation” RNA Biology 9(9):1123-8. 

Bernstein D.A.*, Rolfe A.P.*, Grisafi P., Fink G.R., Gifford D.K. (2012) “Ruler Arrays Reveal Haploid Genome Structural Variation” PLOS1 ;7(8).

Douglas A. Bernstein. (2012) Identification of small molecules that disrupt SSB/protein interactions using a high-throughput screen. “Single-Stranded DNA Binding Proteins: Methods and Protocols” James L. Keck, Methods in Molecular Biology Humana Press, John Walker; 922:183-91.

Bernstein D.A.*, Vyas1 V.K.*, Weinberg D.E., Drinnenberg I.A., Bartel D.P., Fink G.R. (2012) “Candida albicans Dicer (Dcr1) is required for efficient ribosomal and spliceosomal RNA maturation.” Proceedings of the National Academy of Science U S A 109(2):523-8.

Dowell R.D., Ryan O, Jansen A, Cheung D, Agarwala S, Danford T, Bernstein D.A., Rolfe P.A., Heisler L.E., Chin B, Nislow C, Giaever G, Phillips P.C., Fink G.R., Gifford D.K., Boone C. (2010) “Genotype to phenotype: a complex problem.” Science. 328(5977):469.

Bernstein D.A.*, Lu D*, Satyshur K.A., Keck J.L. (2009) “Small-molecule tools for dissecting the roles of SSB/protein interactions in genome maintenance.” Proceedings of the National Academy of Science U S A. 107(2):633-8.

* these authors contributed equally to this work