Which genetic marker for which conservation genetics issue?

被引:172
作者
Wan, QH
Wu, H
Fujihara, T
Fang, SG
机构
[1] Zhejiang Univ, Coll Life Sci, State Conservat Ctr Gene Resources Endangered Wil, Zhejiang 310029, Peoples R China
[2] Zhejiang Univ, Key Lab Conservat Genet & Reprod Biol Endangered, Minist Educ, Zhejiang 310029, Peoples R China
[3] Shimane Univ, Fac Life & Environm Sci, Lab Anim Sci, Matsue, Shimane 690, Japan
关键词
DNA; microsatellites; minisatellites; mitochondrial DNA; oligonucleotide probe; review;
D O I
10.1002/elps.200305922
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Conservation genetics focuses on the effects of contemporary genetic structuring on long-term survival of a species. It helps wildlife managers protect biodiversity by identifying a series of conservation units, which include species, evolutionarily significant units (ESUs) management units (MUs) action units (AUs) and family nets (FNs). Although mito-chondrial DNA (mtDNA) chondrial DNA (mtDNA) evolves 5-10 times faster than single-copy nuclear DNA (scnDNA), it records few traces of contemporary events. Thus, mtDNA can be used to resolve taxonomic uncertainties and ESUs. Variable number of tandem repeats (VNTRs) evolve 100-1000 times faster than scnDNA and provide a powerful tool for analyzing recent and contemporary events. VNTR analysis techniques include polymerase chain reaction (PCR)-based microsatellite assays and oligonucleotide probing. Size homoplasy problems in PCR-based microsatellite assays can strongly affect the inference of recent population history. The high homozygosity in endangered species is reflected in a relatively low number and level of variability in microsatellite loci. This combined with "allelic dropout" and "misprinting" errors contributes to the generation of highly biased genetic data following analyses of natural populations. Thus, in conservation genetics, microsatellites are of limited use for identifying ESUs, MUs, and AUs. In contrast to PCR-based microsatellite analysis, oligonucleotide probing avoids errors resulting from PCR amplification. It is particularly suitable for inferring recent population history and contemporary gene flow between fragmented subpopulations. Oligonucleotide fingerprinting generates individual-specific DNA banding patterns and thus provides a highly precise tool for monitoring demography of natural populations. Hence, DNA fingerprinting is powerful for distinguishing ESUs, MUs, AUs, and FNs. The use of oligonucleotide fingerprinting and fecal DNA is opening new areas for conservation genetics.
引用
收藏
页码:2165 / 2176
页数:12
相关论文
共 90 条
[1]  
ALIS S, 1986, HUM GENET, V74, P239
[2]  
[Anonymous], 1999, WHICH DNA MARKER WHI
[3]  
[Anonymous], 1989, DNA PROBES
[4]   Nuclear markers, mitochondrial DNA and male secondary sexual traits variation in a newt hybrid zone (Triturus vulgaris x T-montandoni) [J].
Babik, W ;
Szymura, JM ;
Rafinski, J .
MOLECULAR ECOLOGY, 2003, 12 (07) :1913-1930
[5]   Amplified fragment length polymorphism analysis identifies hybrids between two subspecies of warblers [J].
Bensch, S ;
Helbig, AJ ;
Salomon, M ;
Siebold, I .
MOLECULAR ECOLOGY, 2002, 11 (03) :473-481
[6]  
Caccone A, 2002, EVOLUTION, V56, P2052
[7]  
CALLEN DF, 1993, AM J HUM GENET, V52, P922
[8]   Contrasted patterns of mitochondrial and nuclear structure among nursery colonies of the bat Myotis myotis [J].
Castella, V ;
Ruedi, M ;
Excoffier, L .
JOURNAL OF EVOLUTIONARY BIOLOGY, 2001, 14 (05) :708-720
[9]  
CIOFI C, 1998, MOL TOOLS SCREENING
[10]  
Clisson I, 2000, AM J PRIMATOL, V50, P205, DOI 10.1002/(SICI)1098-2345(200003)50:3<205::AID-AJP3>3.0.CO