David Brow


Picture of David BrowHector F. DeLuca Biochemical Sciences Building
Room 4204B
440 Henry Mall
Madison WI 53706
Phone: (608) 262-1475
Email: dabrow@wisc.edu
Overview · Publications · Lab Website


BA 1979, University of California, Santa Cruz
PhD 1986, University of California, San Diego
Postdoctoral, 1986-89, University of California, San Francisco (C. Guthrie).

Areas of Study

Biomolecular Folding & Interactions
Gene Expression & RNA Biology
Structural Biology

Research Overview

We study two essential biological "nanomachines" of gene expression, the spliceosome and RNA polymerase II (Pol II), using brewer’s yeast as a model system. Our studies on the spliceosome focus on U6 RNA and the dynamic RNA-RNA and RNA-protein interactions required for its assembly into the active site. Using genetic suppression analysis and in vitro biochemistry, we have defined a complex network of interactions that involves 3 RNAs (U2, U4, and U6), two helicases (Prp28 and Brr2), an RNA-binding protein (Prp24), and the largest and most conserved spliceosomal protein (Prp8). In collaboration with Sam Butcher’s lab, we recently solved the crystal structure of the core U6 snRNP (Prp24 bound to U6 RNA) at 1.7 Å resolution (see Figure 1).

 Crystal structure of the core U6 snRNP

Figure 1. From EJ Montemayor et al. (2014) Nature Struct. Molec. Biol. 21: 544-551.

Our work on Pol II focuses on transcription termination as a strategy for gene regulation. We discovered and are characterizing a pathway that uses the helicase Sen1 and a collection of RNA-binding proteins, including Nrd1 and Nab3, to terminate synthesis of short transcripts by Pol II (see Figure 2). This pathway aids in the synthesis of non-coding RNAs, as well as the regulation of mRNA levels. Mutations in the human homolog of Sen1 result in neurodegenerative disorders. We are exploring the function and targets of the Sen1 termination pathway by genetics, genomics, biochemistry, and structural biology.

Pol II elongation complex with Sen1-Nrd1-Nab3

Figure 2. From DA Brow (2011) Molec. Cell 42: 717-718.