Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures

被引:454
作者
Stark, Alexander
Lin, Michael F.
Kheradpour, Pouya
Pedersen, Jakob S.
Parts, Leopold
Carlson, Joseph W.
Crosby, Madeline A.
Rasmussen, Matthew D.
Roy, Sushmita
Deoras, Ameya N.
Ruby, J. Graham
Brennecke, Julius
Hodges, Emily
Hinrichs, Angie S.
Caspi, Anat
Park, Seung-Won
Han, Mira V.
Maeder, Morgan L.
Polansky, Benjamin J.
Robson, Bryanne E.
Aerts, Stein
van Helden, Jacques
Hassan, Bassem
Gilbert, Donald G.
Eastman, Deborah A.
Rice, Michael
Weir, Michael
Hahn, Matthew W.
Park, Yongkyu
Dewey, Colin N.
Pachter, Lior
Kent, W. James
Haussler, David
Lai, Eric C.
Bartel, David P.
Hannon, Gregory J.
Kaufman, Thomas C.
Eisen, Michael B.
Clark, Andrew G.
Smith, Douglas
Celniker, Susan E.
Gelbart, William M.
Kellis, Manolis [1 ]
机构
[1] MIT, Broad Inst, Cambridge, MA 02140 USA
[2] Harvard Univ, Cambridge, MA 02140 USA
[3] MIT, Comp Sci & Artificial Intelligence Lab, Cambridge, MA 02139 USA
[4] Univ Copenhagen, Dept Mol Biol, DK-2200 Copenhagen N, Denmark
[5] Univ Calif Santa Cruz, Ctr Biomol Sci & Engn, Santa Cruz, CA 95064 USA
[6] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[7] Univ Tartu, Inst Comp Sci, EE-50090 Tartu, Estonia
[8] LBNL, BDGP, Berkeley, CA 94720 USA
[9] Harvard Univ, Biol Labs, Cambridge, MA 02138 USA
[10] Univ New Mexico, Dept Comp Sci, Albuquerque, NM 87131 USA
[11] MIT, Dept Biol, Cambridge, MA 02139 USA
[12] Whitehead Inst, Cambridge, MA 02142 USA
[13] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[14] Univ Calif San Francisco, Berkeley Joint Grad Grp Bioengn, Portland, OR 97210 USA
[15] European Bioinformat Inst, EMBL Nucleotide Sequence Submiss, Cambridge CB10 1SD, England
[16] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Cell Biol & Mol Med, Newark, NJ 07103 USA
[17] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[18] Indiana Univ, Sch Informat, Bloomington, IN 47405 USA
[19] Connecticut Coll, Dept Biol, New London, CT 06320 USA
[20] VIB, Dept Mol & Dev Genet, Neurogenet Lab, B-3000 Louvain, Belgium
[21] Katholieke Univ Leuven, Sch Med, Dept Human Genet, B-3000 Louvain, Belgium
[22] Univ Libre Bruxelles, Dept Biol Mol, B-1050 Brussels, Belgium
[23] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[24] Wesleyan Univ, Dept Math & Comp Sci, Middletown, CT 06459 USA
[25] Wesleyan Univ, Dept Biol, Middletown, CT 06459 USA
[26] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53706 USA
[27] Univ Calif Berkeley, Dept Math, Berkeley, CA 94720 USA
[28] Univ Calif Berkeley, Dept Comp Sci, Berkeley, CA 94720 USA
[29] Mem Sloan Kettering Canc Ctr, Dept Dev Biol, New York, NY 10021 USA
[30] Univ Calif Berkeley, Dept Mol & Cell Biol, Grad Grp Biophys, Berkeley, CA 94720 USA
[31] Univ Calif Berkeley, Ctr Integrat Genom, Berkeley, CA 94720 USA
[32] Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[33] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[34] Agencourt Biosci Corp, Beverly, MA 01915 USA
[35] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1038/nature06340
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sequencing of multiple related species followed by comparative genomics analysis constitutes a powerful approach for the systematic understanding of any genome. Here, we use the genomes of 12 Drosophila species for the de novo discovery of functional elements in the fly. Each type of functional element shows characteristic patterns of change, or 'evolutionary signatures', dictated by its precise selective constraints. Such signatures enable recognition of new protein-coding genes and exons, spurious and incorrect gene annotations, and numerous unusual gene structures, including abundant stop-codon readthrough. Similarly, we predict non-protein-coding RNA genes and structures, and new microRNA (miRNA) genes. We provide evidence of miRNA processing and functionality from both hairpin arms and both DNA strands. We identify several classes of pre- and post-transcriptional regulatory motifs, and predict individual motif instances with high confidence. We also study how discovery power scales with the divergence and number of species compared, and we provide general guidelines for comparative studies.
引用
收藏
页码:219 / 232
页数:14
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