Construction of a BAC contig map of chromosome 16q by two-dimensional overgo hybridization

Citation
Cs. Han et al., Construction of a BAC contig map of chromosome 16q by two-dimensional overgo hybridization, GENOME RES, 10(5), 2000, pp. 714-721
Citations number
17
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENOME RESEARCH
ISSN journal
10889051 → ACNP
Volume
10
Issue
5
Year of publication
2000
Pages
714 - 721
Database
ISI
SICI code
1088-9051(200005)10:5<714:COABCM>2.0.ZU;2-4
Abstract
We have used sequence-based markers From an integrated YAC STS-content/soma tic cell hybrid breakpoint physical map and radiation hybrid maps of human chromosome 16 to construct a new sequence-ready BAC map of the long arm of this chromosome. The integrated physical map was generated previously in ou r laboratory and contains 1150 STSs, providing a marker on average every 78 kb on the euchromatic arms of chromosome 16. The other two maps used for t his effort were the radiation hybrid maps of chromosome 16 from Whitehead I nstitute and Stanford University. To create large sequenceable targets of t his chromosome, we used a systematic approach to screen high-density BAC Fi lters with probes generated from overlapping oligonucleotides (overgos). We first identified all available sequences in the three maps. These include sequences from genes, ESTs, STSs, and cosmid end sequences. We then used BL ASTto identify 36-bp unique fragments of DNA for over go probes. A total of 906 overgos were selected from the long arm of chromosome 16. Hybridizatio ns occurred in thr ee stages: (I) superpool hybridizations against the 12x coverage human BAC library (RPCI-11); (2) two-dimensional hybridizations ag ainst rearrayed positive BACs identified in the superpool hybridizations; a nd (3) pooled tertiary hybridizations for those overgos that had ambiguous positives remaining after the two-dimensional hybridization. For the superp ool hybridizations, up to 236 overgos have been pooled in a single hybridiz ation against the 12x BAC library. A total of 5187 positive BACs from chrom osome 16q were identified as a result of five superpool hybridizations. The se positive clones were rearrayed on membranes and hybridized with 161 two- dimensional subpools of overgos to determine which BAC clones were positive for individual overgos. An additional 46 tertiary hybridizations were requ ired to resolve ambiguous overgo-BAC relationships. Thus, after a total of 212 hybridizations, we have constructed an initial probe-content BAC map of chromosome 16q consisting of 828 overgo markers and 3363 BACs providing >8 5% coverage of the long arm of this chromosome. The map has been confirmed by the fingerprinting data and BAC end PCR screening.