Mouse regulatory DNA landscapes reveal global principles of cis-regulatory evolution

Jeff Vierstra(University of Washington), Eric Rynes(University of Washington), Richard Sandstrom(University of Washington), Miaohua Zhang(Fred Hutch Cancer Center), Theresa K. Canfield(University of Washington), R. Scott Hansen(University of Washington Medical Center), Sandra Stehling-Sun(University of Washington), Peter J. Sabo(University of Washington), Rachel Byron(Fred Hutch Cancer Center), Richard Humbert(University of Washington), Robert E. Thurman(University of Washington), Audra Johnson(University of Washington), Shinny Vong(University of Washington), Kristen Lee(University of Washington), Daniel Bates(University of Washington), Fidencio Neri(University of Washington), Morgan Diegel(University of Washington), Erika Giste(University of Washington), Eric Haugen(University of Washington), Douglas Dunn(University of Washington), Matthew S. Wilken(University of Washington), Steven Z. Josefowicz(Memorial Sloan Kettering Cancer Center), Robert Samstein(Memorial Sloan Kettering Cancer Center), Kai‐Hsin Chang(University of Washington), Evan E. Eichler(Howard Hughes Medical Institute), Marella de Bruijn(John Radcliffe Hospital), Thomas A. Reh(University of Washington), Arthur I. Skoultchi(Albert Einstein College of Medicine), Alexander Y. Rudensky(Memorial Sloan Kettering Cancer Center), Stuart H. Orkin(Howard Hughes Medical Institute), Thalia Papayannopoulou(University of Washington), Piper M. Treuting(University of Washington), Licia Selleri(Cornell University), Rajinder Kaul(University of Washington), Mark Groudine(University of Washington), M. A. Bender(University of Washington), J Stamatoyannopoulos(University of Washington)
Science
November 20, 2014
Cited by 296

Abstract

To study the evolutionary dynamics of regulatory DNA, we mapped >1.3 million deoxyribonuclease I-hypersensitive sites (DHSs) in 45 mouse cell and tissue types, and systematically compared these with human DHS maps from orthologous compartments. We found that the mouse and human genomes have undergone extensive cis-regulatory rewiring that combines branch-specific evolutionary innovation and loss with widespread repurposing of conserved DHSs to alternative cell fates, and that this process is mediated by turnover of transcription factor (TF) recognition elements. Despite pervasive evolutionary remodeling of the location and content of individual cis-regulatory regions, within orthologous mouse and human cell types the global fraction of regulatory DNA bases encoding recognition sites for each TF has been strictly conserved. Our findings provide new insights into the evolutionary forces shaping mammalian regulatory DNA landscapes.


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