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PMID: 12176935 Published · ppublish English Comparative Study Journal Article Validation Study

Parallel construction of orthologous sequence-ready clone contig maps in multiple species.

Genome research ·Vol. 12 ·No. 8 ·2002-08-00 ·Pages 1277-85

Thomas JW, Prasad AB, Summers TJ, Lee-Lin SQ, Maduro VV, Idol JR, Ryan JF, Thomas PJ, McDowell JC, Green ED

Abstract

Comparison is a fundamental tool for analyzing DNA sequence. Interspecies sequence comparison is particularly powerful for inferring genome function and is based on the simple premise that conserved sequences are likely to be important. Thus, the comparison of a genomic sequence with its orthologous counterpart from another species is increasingly becoming an integral component of genome analysis. In ideal situations, such comparisons are performed with orthologous sequences from multiple species. To facilitate multispecies comparative sequence analysis, a robust and scalable strategy for simultaneously constructing sequence-ready bacterial artificial chromosome (BAC) contig maps from targeted genomic regions has been developed. Central to this approach is the generation and utilization of "universal" oligonucleotide-based hybridization probes ("overgo" probes), which are designed from sequences that are highly conserved between distantly related species. Large collections of these probes are used en masse to screen BAC libraries from multiple species in parallel, with the isolated clones assembled into physical contig maps. To validate the effectiveness of this strategy, efforts were focused on the construction of BAC-based physical maps from multiple mammalian species (chimpanzee, baboon, cat, dog, cow, and pig). Using available human and mouse genomic sequence and a newly developed computer program to design the requisite probes, sequence-ready maps were constructed in all species for a series of targeted regions totaling approximately 16 Mb in the human genome. The described approach can be used to facilitate the multispecies comparative sequencing of targeted genomic regions and can be adapted for constructing BAC contig maps in other vertebrates.

MeSH Terms
Animals Cats Cattle Chromosomes, Artificial, Bacterial/genetics Cloning, Molecular/methods Contig Mapping/methods DNA/genetics DNA Probes/genetics Dogs Genome Genome, Human Genomic Library Humans Internet Mice Nucleic Acid Hybridization/methods Pan troglodytes Papio Sequence Homology, Nucleic Acid Species Specificity Swine
Chemicals
DNA Probes DNA
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Thomas James W
Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Prasad Arjun B
Summers Tyrone J
Lee-Lin Shih-Queen
Maduro Valerie V B
Idol Jacquelyn R
Ryan Joseph F
Thomas Pamela J
McDowell Jennifer C
Green Eric D
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Article Info
Journal
Genome research
Abbr.
Genome Res
ISSN
1088-9051
Published
2002-08-00
Pages
1277-85
Language
English
Region
United States
NLM ID
9518021
PMCID
PMC186643
Subset
IM
Analysis Services
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