- PhD, 1997, Stanford University
- BS, 1990, Biological Sciences, Stanford University
Research SummaryWe aim to understand the code for RNA splicing: how the precise locations of introns and splice sites are identified in primary transcripts and how its specificity changes in different cell types. Toward this end, we are mapping the RNA-binding affinity spectra of dozens of human RNA-binding proteins and integrating this information with in vivo binding and activity data. We are also studying the functions of 3’ untranslated regions, including their roles in mRNA localization and microRNA regulation. The lab uses a combination of computational and experimental approaches to address these questions.
- Schering-Plough Research Institute Award (ASBMB), 2007
- Overton Prize for Computational Biology (ISCB), 2001
- Distal Alternative Last Exons Localize mRNAs to Neural Projections. Taliaferro, JM, Vidaki, M, Oliveira, R, Olson, S, Zhan, L, Saxena, T, Wang, ET, Graveley, BR, Gertler, FB, Swanson, MS et al.. 2016. Mol. Cell 61, 821-33.
- Evolutionary dynamics of gene and isoform regulation in Mammalian tissues. Merkin, J, Russell, C, Chen, P, Burge, CB. 2012. Science 338, 1593-9.
- Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins. Wang, ET, Cody, NA, Jog, S, Biancolella, M, Wang, TT, Treacy, DJ, Luo, S, Schroth, GP, Housman, DE, Reddy, S et al.. 2012. Cell 150, 710-24.
- Alternative isoform regulation in human tissue transcriptomes. Wang, ET, Sandberg, R, Luo, S, Khrebtukova, I, Zhang, L, Mayr, C, Kingsmore, SF, Schroth, GP, Burge, CB. 2008. Nature 456, 470-6.
- Proliferating cells express mRNAs with shortened 3' untranslated regions and fewer microRNA target sites. Sandberg, R, Neilson, JR, Sarma, A, Sharp, PA, Burge, CB. 2008. Science 320, 1643-7.