Close sequence comparisons are sufficient to identify human cis-regulatory elements. Export

@article{citeulike:698675, abstract = {Cross-species DNA sequence comparison is the primary method used to identify functional noncoding elements in human and other large genomes. However, little is known about the relative merits of evolutionarily close and distant sequence comparisons. To address this problem, we identified evolutionarily conserved noncoding regions in primate, mammalian, and more distant comparisons using a uniform approach (Gumby) that facilitates unbiased assessment of the impact of evolutionary distance on predictive power. We benchmarked computational predictions against previously identified cis-regulatory elements at diverse genomic loci and also tested numerous extremely conserved human-rodent sequences for transcriptional enhancer activity using an in vivo enhancer assay in transgenic mice. Human regulatory elements were identified with acceptable sensitivity (53\%-80\%) and true-positive rate (27\%-67\%) by comparison with one to five other eutherian mammals or six other simian primates. More distant comparisons (marsupial, avian, amphibian, and fish) failed to identify many of the empirically defined functional noncoding elements. Our results highlight the practical utility of close sequence comparisons, and the loss of sensitivity entailed by more distant comparisons. We derived an intuitive relationship between ancient and recent noncoding sequence conservation from whole-genome comparative analysis that explains most of the observations from empirical benchmarking. Lastly, we determined that, in addition to strength of conservation, genomic location and/or density of surrounding conserved elements must also be considered in selecting candidate enhancers for in vivo testing at embryonic time points.}, address = {Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA;}, author = {Prabhakar, Shyam and Poulin, Francis and Shoukry, Malak and Afzal, Veena and Rubin, Edward M. and Couronne, Olivier and Pennacchio, Len A.}, citeulike-article-id = {698675}, citeulike-linkout-0 = {http://dx.doi.org/10.1101/gr.4717506}, citeulike-linkout-1 = {http://www.genome.org/cgi/content/abstract/16/7/855}, citeulike-linkout-2 = {http://view.ncbi.nlm.nih.gov/pubmed/16769978}, citeulike-linkout-3 = {http://www.hubmed.org/display.cgi?uids=16769978}, day = {12}, doi = {10.1101/gr.4717506}, issn = {1088-9051}, journal = {Genome research}, keywords = {footprinting, mammals, tfbs, transcription}, month = {July}, number = {7}, pages = {855--863}, posted-at = {2006-07-04 15:25:52}, priority = {2}, title = {Close sequence comparisons are sufficient to identify human cis-regulatory elements.}, url = {http://dx.doi.org/10.1101/gr.4717506}, volume = {16}, year = {2006} }

TY - JOUR ID - citeulike:698675 L3 - citeulike-article-id:698675 N2 - Cross-species DNA sequence comparison is the primary method used to identify functional noncoding elements in human and other large genomes. However, little is known about the relative merits of evolutionarily close and distant sequence comparisons. To address this problem, we identified evolutionarily conserved noncoding regions in primate, mammalian, and more distant comparisons using a uniform approach (Gumby) that facilitates unbiased assessment of the impact of evolutionary distance on predictive power. We benchmarked computational predictions against previously identified cis-regulatory elements at diverse genomic loci and also tested numerous extremely conserved human-rodent sequences for transcriptional enhancer activity using an in vivo enhancer assay in transgenic mice. Human regulatory elements were identified with acceptable sensitivity (53%-80%) and true-positive rate (27%-67%) by comparison with one to five other eutherian mammals or six other simian primates. More distant comparisons (marsupial, avian, amphibian, and fish) failed to identify many of the empirically defined functional noncoding elements. Our results highlight the practical utility of close sequence comparisons, and the loss of sensitivity entailed by more distant comparisons. We derived an intuitive relationship between ancient and recent noncoding sequence conservation from whole-genome comparative analysis that explains most of the observations from empirical benchmarking. Lastly, we determined that, in addition to strength of conservation, genomic location and/or density of surrounding conserved elements must also be considered in selecting candidate enhancers for in vivo testing at embryonic time points. IS - 7 JF - Genome research SN - 1088-9051 AD - Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA; EP - 863 TI - Close sequence comparisons are sufficient to identify human cis-regulatory elements. VL - 16 SP - 855 KW - footprinting KW - mammals KW - tfbs KW - transcription AU - Prabhakar, Shyam AU - Poulin, Francis AU - Shoukry, Malak AU - Afzal, Veena AU - Rubin, Edward AU - Couronne, Olivier AU - Pennacchio, Len PY - 2006/07/12/ UR - http://dx.doi.org/10.1101/gr.4717506 ER -