PCR PRIMED WITH VNTR CORE SEQUENCES YIELDS SPECIES-SPECIFIC PATTERNS AND HYPERVARIABLE PROBES

被引:124
作者
HEATH, DD
IWAMA, GK
DEVLIN, RH
机构
[1] FISHERIES & OCEANS CANADA,W VANCOUVER LAB,4160 MARINE DR,W VANCOUVER V7V 1N6,BC,CANADA
[2] UNIV BRITISH COLUMBIA,DEPT ANIM SCI,VANCOUVER V6T 1Z4,BC,CANADA
[3] UNIV BRITISH COLUMBIA,CANADIAN BACTERIAL DIS NETWORK,VANCOUVER V6T 1Z4,BC,CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1093/nar/21.24.5782
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of genomic DNA-based techniques in ecological and evolutionary studies has been limited by the availability of suitable probes for species of interest due to the technical difficulty of isolating and applying such probes. We have developed a simple technique that directs polymerase chain reaction (PCR) amplification to regions rich in variable number of tandem repeats (VNTRs). By using published VNTR core sequences as primers in PCRs, fragments were amplified that showed little variation within a species, but did show differences between species. When the amplified fragments were used as probes with genomic DNA Southern blots they produced hypervariable single-locus or few-locus patterns in fish, birds, and humans. We have named this procedure as Directed Amplification of Minisatellite-region DNA (DAMD).
引用
收藏
页码:5782 / 5785
页数:4
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