A set of canine interrepeat sequence PCR markers for high-throughput genotyping

被引:4
作者
Das, M
Sakul, H
Kong, J
Acland, GM
Pelletier, J
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Dept Oncol, Montreal, PQ H3G 1Y6, Canada
[3] Dept Stat Genet, Parke Davis Lab Mol Genet, Alameda, CA 94502 USA
[4] Cornell Univ, New York State Coll Vet Med, James A Baker Inst Anim Hlth, Ithaca, NY 14853 USA
关键词
IRS-PCR markers; Canis familiaris; genotyping; polymorphism; radiation hybrid mapping; polymerase chain reaction; interspersed repetitive DNA sequence;
D O I
10.1152/physiolgenomics.2000.4.1.13
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
One hundred and sixteen interspersed repetitive DNA sequence (IRS)-PCR markers have been developed and characterized from Canis familiaris for high-throughput filter-based genotyping. We present a detailed analysis of markers produced by amplification using primers directed to the conserved regions of the C. familiaris short interspersed nuclear element (Can-SINE). The majority of IRS-PCR markers developed were moderately to highly polymorphic with mean heterozygosity (HET) and polymorphism information content (PIC) values of similar to0.6. The HET value for 22.3% of the markers exceeded 0.7. We also demonstrate that sequence variation of Can-SINEs between breeds is significant and also represents a rich source of polymorphisms. Mapping of 73 of the markers to the existing integrated linkage-radiation hybrid map enriches the map as well as establishes the utility of the markers. The significance and utility of this new class of IRS-PCR Can-SINE-based markers for high-throughput genotyping is discussed. This method can also be extended to other species that are currently map-poor but have a sufficiently high density of SINEs to allow IRS-PCR.
引用
收藏
页码:13 / 24
页数:12
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