Brian Clay Oliver, Ph.D.

Senior Investigator

Developmental Genomics Section, Laboratory of Cellular and Developmental Biology

NIDDK

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Building 50, Room 3339
50 South Dr
Bethesda, MD 20814

+1 000 000 0000

brian.oliver@nih.gov

Research Topics

Our ultimate goal is to determine how the collective action of genes results in an individual with specific characteristics, development, and disease susceptibilities.

Current Research

Drosophila melanogaster is an important functional model system, boasting facile genetics, complex organ systems, complex behaviors, and a sequenced genome. Our long-term goal is to develop predictive models of gene function with a specific focus on sex differentiation in the germline. Our approach relies on high-throughput techniques used to profile biological processes such as expression, promoter occupancy, and chromatin status, in conjunction with computational analysis and genetics.

Applying our Research

Subtle perturbations in gene networks are likely to cause much of inherited disease susceptibility, but understanding how complex genotypes and environmental interactions result in disease will require experimental systems biology using model organisms. Predictive models for gene and pathway function will be important for diagnosis and ultimately intervention, fulfilling the promise of the human genome project.

Need for Further Study

We have a reasonable understanding of the functions of some individual genes, but we know very little about how they work together.

Biography

Postdoctoral, Stanford University
Ph.D., Case Western Reserve University School of Medicine
M.S., Iowa State University of Science and Technology
B.A., Gustavus Adolphus College

Selected Publications

Wang Y, Cho DY, Lee H, Fear J, Oliver B, Przytycka TM. Reprogramming of regulatory network using expression uncovers sex-specific gene regulation in Drosophila. Nat Commun. 2018;9(1):4061.
Yang H, Jaime M, Polihronakis M, Kanegawa K, Markow T, Kaneshiro K, Oliver B. Re-annotation of eight <i>Drosophila</i> genomes. Life Sci Alliance. 2018;1(6):e201800156.
Lee H, Cho DY, Whitworth C, Eisman R, Phelps M, Roote J, Kaufman T, Cook K, Russell S, Przytycka T, Oliver B. Effects of Gene Dose, Chromatin, and Network Topology on Expression in Drosophila melanogaster. PLoS Genet. 2016;12(9):e1006295.
Yang H, Basquin D, Pauli D, Oliver B. Drosophila melanogaster positive transcriptional elongation factors regulate metabolic and sex-biased expression in adults. BMC Genomics. 2017;18(1):384.
Chen ZX, Sturgill D, Qu J, Jiang H, Park S, Boley N, Suzuki AM, Fletcher AR, Plachetzki DC, FitzGerald PC, Artieri CG, Atallah J, Barmina O, Brown JB, Blankenburg KP, Clough E, Dasgupta A, Gubbala S, Han Y, Jayaseelan JC, Kalra D, Kim YA, Kovar CL, Lee SL, Li M, Malley JD, Malone JH, Mathew T, Mattiuzzo NR, Munidasa M, Muzny DM, Ongeri F, Perales L, Przytycka TM, Pu LL, Robinson G, Thornton RL, Saada N, Scherer SE, Smith HE, Vinson C, Warner CB, Worley KC, Wu YQ, Zou X, Cherbas P, Kellis M, Eisen MB, Piano F, Kionte K, Fitch DH, Sternberg PW, Cutter AD, Duff MO, Hoskins RA, Graveley BR, Gibbs RA, Bickel PJ, Kopp A, Carninci P, Celniker SE, Oliver B, Richards S. Comparative validation of the D. melanogaster modENCODE transcriptome annotation. Genome Res. 2014;24(7):1209-23.