Martha L. Bulyk
Division of Genetics, Department of Medicine; Department of Pathology
Harvard-MIT Division of Health Sciences & Technology (HST), Associate Member of The Broad Institute of MIT and Harvard
New Research Building, Room 466D
77 Avenue Louis Pasteur
Boston, MA 02115
Tel: 617-525-4725
Fax: 617-525-4705
Email: mlbulyk@receptor.med.harvard.edu
Lab Members: 2 postdoctoral fellows, 3 graduate students, 2 lab technicians
Visit my lab page here.
Although numerous eukaryotic genomes have been sequenced, much still remains to be understood about how the genes in those genomes are regulated. The interactions between transcription factors (TFs) and their DNA binding sites are an integral part of the regulatory networks within cells. We employ numerous combined experimental and computational strategies in studying these regulatory interactions, to discover cis regulatory codes in the genome.
To permit a genome-wide scan of all possible TF binding sites in a given genome, we developed universal protein binding microarrays (PBMs), a DNA microarray-based technology that allows rapid, high-throughput characterization of the DNA binding site sequence specificities of proteins. We are using PBMs to study hundreds of TFs in Drosophila and mammals, so that we may predict sets of co-regulatory TFs acting together at candidate transcriptional cis regulatory modules, such as transcriptional enhancers. We are examining the effects of protein-protein interactions in DNA binding. We are also investigating divergence within TF families and how different members of a TF family gain distinct regulatory roles. We are investigating the effects of mutations and naturally occurring genetic variation on human TFs. We are combining sequence, evolutionary, structural, and PBM data to understand the molecular determinants of protein-DNA binding specificity and its evolution. We have developed computational strategies that employ comparative genomics methods for prediction of tissue-specific transcriptional enhancers in fly, and separately in mammals. Many of these predicted enhancers recently have been validated in vivo. In our analyses, we infer each TF’s relative importance for a given cell-type-specific gene expression pattern. We are interested in understanding the quantitative nature of information encoded within transcriptional enhancers, as it pertains to spatiotemporal specificity of enhancer activity. Technology development projects include novel approaches for high-throughput, experimental identification of tissue/cell-type-specific enhancers. The results of these experiments and analyses aim for a better understanding of the functions, locations and organization of DNA regulatory elements, and their evolution.
References: (*co-1st authors; †co-corresponding authors):
*Siggers T, *Chang AB, Teixeira A, Wong D, Williams KJ, Ahmed B, Ragoussis J, Udalova IA, Smale ST, Bulyk ML. Principles of dimer-specific gene regulation revealed by a comprehensive characterization of NF-kB family DNA binding. Nature Immunology (2012) 13(1):95-102.
Siggers T, Duyzend M, Reddy J, Kahn S, Bulyk ML. Non-DNA-binding cofactors enhance DNA-binding specificity of a transcriptional regulatory complex. Molecular Systems Biology (2011) 7:555.
*Rowan S, *Siggers T, Lachke S, Yue Y, Copeland NG, Blasi F, †Bulyk ML, †Maas RL. Precise temporal control of the eye regulatory gene Pax6 via enhancer binding site affinity. Genes & Development (2010) 24:980-985.
*Badis G, *Berger MF, *Philippakis AA, *Talukder S, *Gehrke AR, *Jaeger SA, *Chan ET, Metzler G, Vedenko A, Chen X, Kuznetsov H, Wang C-F, Coburn D, Newburger D, Morris QD, †Hughes TR, †Bulyk ML. Diversity and complexity in DNA recognition by transcription factors. Science (2009) 324:1720-1723.
For a complete listing of publications click here.
Last Update: 7/26/2012