Construction and Characterization of a 10-fold Genome Equivalent Rat P1-Derived Artificial Chromosome Library |
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Authors: | Peng Yeong Woon Kazutoyo Osoegawa Pamela J. Kaisaki Baohui Zhao Joseph J. Catanese Dominique Gauguier Roger Cox Elaine R. Levy G.Mark Lathrop Anthony P. Monaco Pieter J. de Jong |
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Affiliation: | aThe Wellcome Trust Centre For Human Genetics, University of Oxford, Windmill Road, Headington, OX3 7BN, Oxford, United Kingdom;bHuman Genetics Department, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, New York, 14263 |
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Abstract: | A rat PAC library was constructed in the vector pPAC4 from genomic DNA isolated from female Brown Norway rats. This library consists of 215,409 clones arrayed in 614 384-well microtiter plates. An average insert size of 143 kb was estimated from 217 randomly isolated clones, thus representing approximately 10-fold genome coverage. This coverage provides a very high probability that the library contains a unique sequence in genome screening. Tests on randomly selected clones demonstrated that they are very stable, with only 4 of 130 clones showing restriction digest fragment alterations after 80 generations of serial growth. FISH analysis using 70 randomly chosen PACs revealed no significant chimeric clones. About 7% of the clones analyzed contained repetitive sequences related to centromeric regions that hybridized to some but not all centromeres. DNA plate pools and superpools were made, and high-density filters each containing an array of 8 plates in duplicate were prepared. Library screening on these superpools and appropriate filters with 10 single-locus rat markers revealed an average of 8 positive clones, in agreement with the estimated high genomic coverage of this library and representation of the rat genome. This library provides a new resource for rat genome analysis, in particular the identification of genes involved in models of multifactorial disease. The library and high-density filters are currently available to the scientific community. |
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