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A high-resolution map of human evolutionary constraint using 29 mammals.

Authors :
Lindblad-Toh K
Garber M
Zuk O
Lin MF
Parker BJ
Washietl S
Kheradpour P
Ernst J
Jordan G
Mauceli E
Ward LD
Lowe CB
Holloway AK
Clamp M
Gnerre S
Alföldi J
Beal K
Chang J
Clawson H
Cuff J
Di Palma F
Fitzgerald S
Flicek P
Guttman M
Hubisz MJ
Jaffe DB
Jungreis I
Kent WJ
Kostka D
Lara M
Martins AL
Massingham T
Moltke I
Raney BJ
Rasmussen MD
Robinson J
Stark A
Vilella AJ
Wen J
Xie X
Zody MC
Baldwin J
Bloom T
Chin CW
Heiman D
Nicol R
Nusbaum C
Young S
Wilkinson J
Worley KC
Kovar CL
Muzny DM
Gibbs RA
Cree A
Dihn HH
Fowler G
Jhangiani S
Joshi V
Lee S
Lewis LR
Nazareth LV
Okwuonu G
Santibanez J
Warren WC
Mardis ER
Weinstock GM
Wilson RK
Delehaunty K
Dooling D
Fronik C
Fulton L
Fulton B
Graves T
Minx P
Sodergren E
Birney E
Margulies EH
Herrero J
Green ED
Haussler D
Siepel A
Goldman N
Pollard KS
Pedersen JS
Lander ES
Kellis M
Source :
Nature [Nature] 2011 Oct 12; Vol. 478 (7370), pp. 476-82. Date of Electronic Publication: 2011 Oct 12.
Publication Year :
2011

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.

Details

Language :
English
ISSN :
1476-4687
Volume :
478
Issue :
7370
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
21993624
Full Text :
https://doi.org/10.1038/nature10530