A high-resolution map of human evolutionary constraint using 29 mammals.
| dc.contributor.author | Lindblad-Toh, Kerstin | |
| dc.contributor.author | Garber, Manuel | |
| dc.contributor.author | Zuk, Or | |
| dc.contributor.author | Lin, Michael F | |
| dc.contributor.author | Parker, Brian J | |
| dc.contributor.author | Washietl, Stefan | |
| dc.contributor.author | Kheradpour, Pouya | |
| dc.contributor.author | Ernst, Jason | |
| dc.contributor.author | Jordan, Gregory | |
| dc.contributor.author | Mauceli, Evan | |
| dc.contributor.author | Ward, Lucas D | |
| dc.contributor.author | Lowe, Craig B | |
| dc.contributor.author | Holloway, Alisha K | |
| dc.contributor.author | Clamp, Michele | |
| dc.contributor.author | Gnerre, Sante | |
| dc.contributor.author | Alföldi, Jessica | |
| dc.contributor.author | Beal, Kathryn | |
| dc.contributor.author | Chang, Jean | |
| dc.contributor.author | Clawson, Hiram | |
| dc.contributor.author | Cuff, James | |
| dc.contributor.author | Di Palma, Federica | |
| dc.contributor.author | Fitzgerald, Stephen | |
| dc.contributor.author | Flicek, Paul | |
| dc.contributor.author | Guttman, Mitchell | |
| dc.contributor.author | Hubisz, Melissa J | |
| dc.contributor.author | Jaffe, David B | |
| dc.contributor.author | Jungreis, Irwin | |
| dc.contributor.author | Kent, W James | |
| dc.contributor.author | Kostka, Dennis | |
| dc.contributor.author | Lara, Marcia | |
| dc.contributor.author | Martins, Andre L | |
| dc.contributor.author | Massingham, Tim | |
| dc.contributor.author | Moltke, Ida | |
| dc.contributor.author | Raney, Brian J | |
| dc.contributor.author | Rasmussen, Matthew D | |
| dc.contributor.author | Robinson, Jim | |
| dc.contributor.author | Stark, Alexander | |
| dc.contributor.author | Vilella, Albert J | |
| dc.contributor.author | Wen, Jiayu | |
| dc.contributor.author | Xie, Xiaohui | |
| dc.contributor.author | Zody, Michael C | |
| dc.contributor.author | Broad Institute Sequencing Platform and Whole Genome Assembly Team | |
| dc.contributor.author | Baldwin, Jen | |
| dc.contributor.author | Bloom, Toby | |
| dc.contributor.author | Chin, Chee Whye | |
| dc.contributor.author | Heiman, Dave | |
| dc.contributor.author | Nicol, Robert | |
| dc.contributor.author | Nusbaum, Chad | |
| dc.contributor.author | Young, Sarah | |
| dc.contributor.author | Wilkinson, Jane | |
| dc.contributor.author | Worley, Kim C | |
| dc.contributor.author | Kovar, Christie L | |
| dc.contributor.author | Muzny, Donna M | |
| dc.contributor.author | Gibbs, Richard A | |
| dc.contributor.author | Baylor College of Medicine Human Genome Sequencing Center Sequencing Team | |
| dc.contributor.author | Cree, Andrew | |
| dc.contributor.author | Dihn, Huyen H | |
| dc.contributor.author | Fowler, Gerald | |
| dc.contributor.author | Jhangiani, Shalili | |
| dc.contributor.author | Joshi, Vandita | |
| dc.contributor.author | Lee, Sandra | |
| dc.contributor.author | Lewis, Lora R | |
| dc.contributor.author | Nazareth, Lynne V | |
| dc.contributor.author | Okwuonu, Geoffrey | |
| dc.contributor.author | Santibanez, Jireh | |
| dc.contributor.author | Warren, Wesley C | |
| dc.contributor.author | Mardis, Elaine R | |
| dc.contributor.author | Weinstock, George M | |
| dc.contributor.author | Wilson, Richard K | |
| dc.contributor.author | Genome Institute at Washington University | |
| dc.contributor.author | Delehaunty, Kim | |
| dc.contributor.author | Dooling, David | |
| dc.contributor.author | Fronik, Catrina | |
| dc.contributor.author | Fulton, Lucinda | |
| dc.contributor.author | Fulton, Bob | |
| dc.contributor.author | Graves, Tina | |
| dc.contributor.author | Minx, Patrick | |
| dc.contributor.author | Sodergren, Erica | |
| dc.contributor.author | Birney, Ewan | |
| dc.contributor.author | Margulies, Elliott H | |
| dc.contributor.author | Herrero, Javier | |
| dc.contributor.author | Green, Eric D | |
| dc.contributor.author | Haussler, David | |
| dc.contributor.author | Siepel, Adam | |
| dc.contributor.author | Goldman, Nick | |
| dc.contributor.author | Pollard, Katherine S | |
| dc.contributor.author | Pedersen, Jakob S | |
| dc.contributor.author | Lander, Eric S | |
| dc.contributor.author | Kellis, Manolis | |
| dc.date.accessioned | 2018-09-13T14:41:07Z | |
| dc.date.available | 2018-09-13T14:41:07Z | |
| dc.date.issued | 2011-10-12 | |
| dc.date.updated | 2018-09-13T14:41:06Z | |
| dc.description.abstract | The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we report the sequencing and comparative analysis of 29 eutherian genomes. We confirm that at least 5.5% of the human genome has undergone purifying selection, and locate constrained elements covering ∼4.2% of the genome. We use evolutionary signatures and comparisons with experimental data sets to suggest candidate functions for ∼60% of constrained bases. These elements reveal a small number of new coding exons, candidate stop codon readthrough events and over 10,000 regions of overlapping synonymous constraint within protein-coding exons. We find 220 candidate RNA structural families, and nearly a million elements overlapping potential promoter, enhancer and insulator regions. We report specific amino acid residues that have undergone positive selection, 280,000 non-coding elements exapted from mobile elements and more than 1,000 primate- and human-accelerated elements. Overlap with disease-associated variants indicates that our findings will be relevant for studies of human biology, health and disease. | |
| dc.identifier.issn | 0028-0836 | |
| dc.identifier.issn | 1476-4687 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Springer Science and Business Media LLC | |
| dc.relation.ispartof | Nature | |
| dc.relation.isversionof | 10.1038/nature10530 | |
| dc.subject | Broad Institute Sequencing Platform and Whole Genome Assembly Team | |
| dc.subject | Baylor College of Medicine Human Genome Sequencing Center Sequencing Team | |
| dc.subject | Genome Institute at Washington University | |
| dc.subject | Animals | |
| dc.subject | Mammals | |
| dc.subject | Humans | |
| dc.subject | Disease | |
| dc.subject | RNA | |
| dc.subject | Sequence Alignment | |
| dc.subject | Sequence Analysis, DNA | |
| dc.subject | Genomics | |
| dc.subject | Evolution, Molecular | |
| dc.subject | Phylogeny | |
| dc.subject | Genome | |
| dc.subject | Genome, Human | |
| dc.subject | Exons | |
| dc.subject | Health | |
| dc.subject | Selection, Genetic | |
| dc.subject | Molecular Sequence Annotation | |
| dc.title | A high-resolution map of human evolutionary constraint using 29 mammals. | |
| dc.type | Journal article | |
| pubs.begin-page | 476 | |
| pubs.end-page | 482 | |
| pubs.issue | 7370 | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | Molecular Genetics and Microbiology | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.publication-status | Published | |
| pubs.volume | 478 |
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