Genome-Wide Location and Function of DNA Binding Proteins

Author:

Ren Bing1,Robert François1,Wyrick John J.12,Aparicio Oscar23,Jennings Ezra G.12,Simon Itamar1,Zeitlinger Julia1,Schreiber Jörg1,Hannett Nancy1,Kanin Elenita1,Volkert Thomas L.1,Wilson Christopher J.4,Bell Stephen P.25,Young Richard A.12

Affiliation:

1. Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.

2. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

3. Program in Molecular Biology University of Southern California, Los Angeles, CA 90089–1340, USA.

4. Corning, Inc., Corning, NY 14834, USA.

5. Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Abstract

Understanding how DNA binding proteins control global gene expression and chromosomal maintenance requires knowledge of the chromosomal locations at which these proteins function in vivo. We developed a microarray method that reveals the genome-wide location of DNA-bound proteins and used this method to monitor binding of gene-specific transcription activators in yeast. A combination of location and expression profiles was used to identify genes whose expression is directly controlled by Gal4 and Ste12 as cells respond to changes in carbon source and mating pheromone, respectively. The results identify pathways that are coordinately regulated by each of the two activators and reveal previously unknown functions for Gal4 and Ste12. Genome-wide location analysis will facilitate investigation of gene regulatory networks, gene function, and genome maintenance.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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