Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library

Genomics. 1998 Jun 15;50(3):306-16. doi: 10.1006/geno.1998.5319.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromosomes / genetics*
  • Chromosomes, Artificial, Yeast
  • Cloning, Molecular / methods*
  • DNA Restriction Enzymes
  • Electrophoresis, Gel, Pulsed-Field
  • Female
  • Genetic Markers
  • Genomic Library*
  • In Situ Hybridization
  • In Situ Hybridization, Fluorescence
  • Metaphase
  • Polymerase Chain Reaction
  • Rats
  • Rats, Inbred BN
  • Time Factors
  • Trinucleotide Repeat Expansion

Substances

  • Genetic Markers
  • DNA Restriction Enzymes