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PMID: 11591642 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Evolutionarily conserved sequences on human chromosome 21.

Genome research ·Vol. 11 ·No. 10 ·2001-10-00 ·Pages 1651-9

Frazer KA, Sheehan JB, Stokowski RP, Chen X, Hosseini R, Cheng JF, Fodor SP, Cox DR, Patil N

Abstract

Comparison of human sequences with the DNA of other mammals is an excellent means of identifying functional elements in the human genome. Here we describe the utility of high-density oligonucleotide arrays as a rapid approach for comparing human sequences with the DNA of multiple species whose sequences are not presently available. High-density arrays representing approximately 22.5 Mb of nonrepetitive human chromosome 21 sequence were synthesized and then hybridized with mouse and dog DNA to identify sequences conserved between humans and mice (human-mouse elements) and between humans and dogs (human-dog elements). Our data show that sequence comparison of multiple species provides a powerful empiric method for identifying actively conserved elements in the human genome. A large fraction of these evolutionarily conserved elements are present in regions on chromosome 21 that do not encode known genes.

MeSH Terms
Animals Chromosomes, Artificial, Bacterial/genetics Chromosomes, Human, Pair 21/genetics Conserved Sequence/genetics DNA/genetics Dogs Evolution, Molecular Genes, Overlapping/genetics Humans Mice Oligonucleotide Array Sequence Analysis/methods Sensitivity and Specificity Synteny/genetics
Chemicals
DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Frazer K A
Perlegen Sciences, Santa Clara, California 95051, USA. [email protected]
Sheehan J B
Stokowski R P
Chen X
Hosseini R
Cheng J F
Fodor S P
Cox D R
Patil N
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Article Info
Journal
Genome research
Abbr.
Genome Res
ISSN
1088-9051
Published
2001-10-00
Pages
1651-9
Language
English
Region
United States
NLM ID
9518021
PMCID
PMC311124
Subset
IM
Grants
NIGMS NIH HHS · GM-5748202 · United States
Corrections
CommentIn
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