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
相关论文
共 43 条
[21]   EFFICIENT HIGH-RESOLUTION GENETIC-MAPPING OF MOUSE INTERSPERSED REPETITIVE SEQUENCE PCR PRODUCTS, TOWARD INTEGRATED GENETIC AND PHYSICAL MAPPING OF THE MOUSE GENOME [J].
MCCARTHY, L ;
HUNTER, K ;
SCHALKWYK, L ;
RIBA, L ;
ANSON, S ;
MOTT, R ;
NEWELL, W ;
BRULEY, C ;
BAR, I ;
RAMU, E ;
HOUSMAN, D ;
COX, R ;
LEHRACH, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5302-5306
[22]   An integrated linkage-radiation hybrid map of the canine genome [J].
Mellersh, CS ;
Hitte, C ;
Richman, M ;
Vignaux, F ;
Priat, C ;
Jouquand, S ;
Werner, P ;
André, C ;
DeRose, S ;
Patterson, DF ;
Ostrander, EA ;
Galibert, F .
MAMMALIAN GENOME, 2000, 11 (02) :120-130
[23]   A HIGHLY REPETITIVE DNA-SEQUENCE POSSIBLY UNIQUE TO CANIDS [J].
MINNICK, MF ;
STILLWELL, LC ;
HEINEMAN, JM ;
STIEGLER, GL .
GENE, 1992, 110 (02) :235-238
[24]   Development of a feline whole genome radiation hybrid panel and comparative mapping of human chromosome 12 and 22 loci [J].
Murphy, WJ ;
Menotti-Raymond, M ;
Lyons, LA ;
Thompson, MA ;
O'Brien, SJ .
GENOMICS, 1999, 57 (01) :1-8
[25]  
Neff MW, 1999, GENETICS, V151, P803
[26]   ALU POLYMERASE CHAIN-REACTION - A METHOD FOR RAPID ISOLATION OF HUMAN-SPECIFIC SEQUENCES FROM COMPLEX DNA SOURCES [J].
NELSON, DL ;
LEDBETTER, SA ;
CORBO, L ;
VICTORIA, MF ;
RAMIREZSOLIS, R ;
WEBSTER, TD ;
LEDBETTER, DH ;
CASKEY, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6686-6690
[27]  
Nock C, 1999, ELECTROPHORESIS, V20, P1027, DOI 10.1002/(SICI)1522-2683(19990101)20:4/5&lt
[28]  
1027::AID-ELPS1027&gt
[29]  
3.0.CO
[30]  
2-I