作者: Sonali Mukherjee , Michael F Berger , Ghil Jona , Xun S Wang , Dale Muzzey
DOI: 10.1038/NG1473
关键词: ChIP-sequencing 、 DNA sequencing 、 DNA binding site 、 TRANSFAC 、 ChIP-on-chip 、 Genetics 、 DNA microarray 、 Sequence analysis 、 Biology 、 Conserved sequence
摘要: We developed a new DNA microarray-based technology, called protein binding microarrays (PBMs), that allows rapid, high-throughput characterization of the in vitro binding-site sequence specificities transcription factors single day. Using PBMs, we identified yeast Abf1, Rap1 and Mig1. Comparison these proteins' sites with their vivo indicates PBM-derived can accurately reflect specificities. In addition to previously targets, Mig1 bound 107, 90 75 putative target intergenic regions, respectively, many which were upstream uncharacterized open reading frames. Comparative analysis indicated newly are highly conserved across five sequenced sensu stricto species and, therefore, probably functional may be used condition-specific manner. Similar PBM experiments should useful identifying cis regulatory elements transcriptional networks various genomes.