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PMID: 22956687 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Evidence of abundant purifying selection in humans for recently acquired regulatory functions.

Science (New York, N.Y.) ·Vol. 337 ·No. 6102 ·2012-09-28 ·Pages 1675-8

Ward LD, Kellis M

Abstract

Although only 5% of the human genome is conserved across mammals, a substantially larger portion is biochemically active, raising the question of whether the additional elements evolve neutrally or confer a lineage-specific fitness advantage. To address this question, we integrate human variation information from the 1000 Genomes Project and activity data from the ENCODE Project. A broad range of transcribed and regulatory nonconserved elements show decreased human diversity, suggesting lineage-specific purifying selection. Conversely, conserved elements lacking activity show increased human diversity, suggesting that some recently became nonfunctional. Regulatory elements under human constraint in nonconserved regions were found near color vision and nerve-growth genes, consistent with purifying selection for recently evolved functions. Our results suggest continued turnover in regulatory regions, with at least an additional 4% of the human genome subject to lineage-specific constraint.

MeSH Terms
Conserved Sequence Disease/genetics Gene Expression Regulation Genetic Variation Genome, Human/genetics Humans Polymorphism, Single Nucleotide Regulatory Sequences, Nucleic Acid/genetics Selection, Genetic Transcription, Genetic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ward Lucas D
Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
Kellis Manolis
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Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2012-09-28
Epub
2012-00-05
Pages
1675-8
Language
English
Region
United States
NLM ID
0404511
PMCID
PMC4104271
Subset
IM
Grants
NHGRI NIH HHS · R01 HG004037 · United States
NHGRI NIH HHS · RC1 HG005334 · United States
NHGRI NIH HHS · R01HG004037 · United States
NHGRI NIH HHS · RC1HG005334 · United States
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