28-way vertebrate alignment and conservation track in the UCSC Genome Browser

被引:211
作者
Miller, Webb [1 ]
Rosenbloom, Kate
Hardison, Ross C.
Hou, Minmei
Taylor, James
Raney, Brian
Burhans, Richard
King, David C.
Baertsch, Robert
Blankenberg, Daniel
Pond, Sergei L. Kosakovsky
Nekrutenko, Anton
Giardine, Belinda
Harris, Robert S.
Diekhans, Svitlana Tyekucheva Mark
Diekhans, Mark
Pringle, Thomas H.
Murphy, William J.
Lesk, Arthur
Weinstock, George M.
Lindblad-Toh, Kerstin
Gibbs, Richard A.
Lander, Eric S.
Siepel, Adam
Haussler, David
Kent, W. James
机构
[1] Penn State Univ, Ctr Comparat Genom & Bioinformat, University Pk, PA 16802 USA
[2] Univ Calif Santa Cruz, Ctr Biomol Sci & Engn, Santa Cruz, CA 95064 USA
[3] NYU, Courant Inst, New York, NY 10012 USA
[4] Univ Calif San Diego, Antiviral Res Ctr, San Diego, CA 92103 USA
[5] Sperling Fdn, Eugene, OR 97405 USA
[6] Texas A&M Univ, Dept Vet Integrat Biosci, College Stn, TX 77843 USA
[7] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[8] Harvard Univ, MIT, Broad Inst, Cambridge, MA 02142 USA
[9] Cornell Univ, Dept Biol Stat & Computat Biol, Ithaca, NY 14853 USA
[10] Howard Hughes Med Inst, Santa Cruz, CA 95060 USA
关键词
D O I
10.1101/gr.6761107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This article describes a set of alignments of 28 vertebrate genome sequences that is provided by the UCSC Genome Browser. The alignments can be viewed on the Human Genome Browser ( March 2006 assembly) at http://genome.ucsc.edu, downloaded in bulk by anonymous FTP from http://hgdownload.cse.ucsc.edu/goldenPath/ hg18/multiz28way, or analyzed with the Galaxy server at http://g2.bx.psu.edu. This article illustrates the power of this resource for exploring vertebrate and mammalian evolution, using three examples. First, we present several vignettes involving insertions and deletions within protein-coding regions, including a look at some human-specific indels. Then we study the extent to which start codons and stop codons in the human sequence are conserved in other species, showing that start codons are in general more poorly conserved than stop codons. Finally, an investigation of the phylogenetic depth of conservation for several classes of functional elements in the human genome reveals striking differences in the rates and modes of decay in alignability. Each functional class has a distinctive period of stringent constraint, followed by decays that allow ( for the case of regulatory regions) or reject ( for coding regions and ultraconserved elements) insertions and deletions.
引用
收藏
页码:1797 / 1808
页数:12
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