{"title":"从鱼鳍夹中提取pcr扩增mtDNA的限制性酶切文摘是对野生种群中数百种鱼类的序列遗传“标签”进行分析的方法。","authors":"R R Wilson, K A Donaldson","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We tested the feasibility of recovering from wild populations mitochondrial DNA genetic \"tags\" that might result from release of hatchery-reared fingerlings for marine stock enhancement. A practical, nondestructive method of genetic \"tag\" recovery would allow quantitative assessment of the efficacy of such programs. A rare mtDNA variant with two sites each instead of one for TaqI and RsaI in the control region was used as a mock genetic \"tag\" in snook (Centropomus undecimalis). We assayed for the variant among nearly 900 fish by restriction digests of DNA amplified by polymerase chain reaction (PCR) obtained from fin-clip extracts, finding only a single second example of the variant. Thus, mtDNA \"tags\" can be nondestructively assayed for with specificity among hundreds of individuals.</p>","PeriodicalId":77273,"journal":{"name":"Molecular marine biology and biotechnology","volume":"7 1","pages":"39-47"},"PeriodicalIF":0.0000,"publicationDate":"1998-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Restriction digest of PCR-amplified mtDNA from fin clips is an assay for sequence genetic \\\"tags\\\" among hundreds of fish in wild populations.\",\"authors\":\"R R Wilson, K A Donaldson\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We tested the feasibility of recovering from wild populations mitochondrial DNA genetic \\\"tags\\\" that might result from release of hatchery-reared fingerlings for marine stock enhancement. A practical, nondestructive method of genetic \\\"tag\\\" recovery would allow quantitative assessment of the efficacy of such programs. A rare mtDNA variant with two sites each instead of one for TaqI and RsaI in the control region was used as a mock genetic \\\"tag\\\" in snook (Centropomus undecimalis). We assayed for the variant among nearly 900 fish by restriction digests of DNA amplified by polymerase chain reaction (PCR) obtained from fin-clip extracts, finding only a single second example of the variant. Thus, mtDNA \\\"tags\\\" can be nondestructively assayed for with specificity among hundreds of individuals.</p>\",\"PeriodicalId\":77273,\"journal\":{\"name\":\"Molecular marine biology and biotechnology\",\"volume\":\"7 1\",\"pages\":\"39-47\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular marine biology and biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular marine biology and biotechnology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Restriction digest of PCR-amplified mtDNA from fin clips is an assay for sequence genetic "tags" among hundreds of fish in wild populations.
We tested the feasibility of recovering from wild populations mitochondrial DNA genetic "tags" that might result from release of hatchery-reared fingerlings for marine stock enhancement. A practical, nondestructive method of genetic "tag" recovery would allow quantitative assessment of the efficacy of such programs. A rare mtDNA variant with two sites each instead of one for TaqI and RsaI in the control region was used as a mock genetic "tag" in snook (Centropomus undecimalis). We assayed for the variant among nearly 900 fish by restriction digests of DNA amplified by polymerase chain reaction (PCR) obtained from fin-clip extracts, finding only a single second example of the variant. Thus, mtDNA "tags" can be nondestructively assayed for with specificity among hundreds of individuals.