{"title":"密歇根樱桃蒙利菌与松拉蒙利菌的遗传变异","authors":"C. Snyder, A. Jones","doi":"10.1080/07060661.1999.10599997","DOIUrl":null,"url":null,"abstract":"Abstract Polymerase chain reaction (PCR)-mediated analysis of rDNA from isolates of Monilinia fructicola and Monilinia laxa from Michigan cheny orchards revealed interspecies restriction site variation in the internal transcribed spacer 1 (ITSI) region and length variation in the small subunit (SSU) rRNA gene. 1TS1 sequences from both species were 146 by long; however, the ITSI of M. laxa differed at three positions from the ITSI of M. fructicola. Although the sequences of the ITS1 regions from both species were nearly identical, the enzyme tilrel cuts the PCR-amplified ITSI region of the two species differentially. PCR amplification of the 3′ end of the SSU rRNA gene yielded products of approximately 940 and 520 by from M. fructicola and M. laxa, respectively. A 421-bp group I intron was detected by PCR within the SSU rDNA of 32 isolates of M. fructicola but not in the eight isolates of M. laxa. Intron sequences from each of four isolates of M. fructicola were identical, and the SSU rDNA flanking sequenc...","PeriodicalId":9607,"journal":{"name":"Canadian Journal of Plant Pathology-revue Canadienne De Phytopathologie","volume":"24 1","pages":"70-77"},"PeriodicalIF":0.0000,"publicationDate":"1999-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"39","resultStr":"{\"title\":\"Genetic variation between strains of Monilinia fructicola and Monilinia laxa isolated from cherries in Michigan\",\"authors\":\"C. Snyder, A. Jones\",\"doi\":\"10.1080/07060661.1999.10599997\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Polymerase chain reaction (PCR)-mediated analysis of rDNA from isolates of Monilinia fructicola and Monilinia laxa from Michigan cheny orchards revealed interspecies restriction site variation in the internal transcribed spacer 1 (ITSI) region and length variation in the small subunit (SSU) rRNA gene. 1TS1 sequences from both species were 146 by long; however, the ITSI of M. laxa differed at three positions from the ITSI of M. fructicola. Although the sequences of the ITS1 regions from both species were nearly identical, the enzyme tilrel cuts the PCR-amplified ITSI region of the two species differentially. PCR amplification of the 3′ end of the SSU rRNA gene yielded products of approximately 940 and 520 by from M. fructicola and M. laxa, respectively. A 421-bp group I intron was detected by PCR within the SSU rDNA of 32 isolates of M. fructicola but not in the eight isolates of M. laxa. Intron sequences from each of four isolates of M. fructicola were identical, and the SSU rDNA flanking sequenc...\",\"PeriodicalId\":9607,\"journal\":{\"name\":\"Canadian Journal of Plant Pathology-revue Canadienne De Phytopathologie\",\"volume\":\"24 1\",\"pages\":\"70-77\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"39\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Canadian Journal of Plant Pathology-revue Canadienne De Phytopathologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/07060661.1999.10599997\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Plant Pathology-revue Canadienne De Phytopathologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/07060661.1999.10599997","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Genetic variation between strains of Monilinia fructicola and Monilinia laxa isolated from cherries in Michigan
Abstract Polymerase chain reaction (PCR)-mediated analysis of rDNA from isolates of Monilinia fructicola and Monilinia laxa from Michigan cheny orchards revealed interspecies restriction site variation in the internal transcribed spacer 1 (ITSI) region and length variation in the small subunit (SSU) rRNA gene. 1TS1 sequences from both species were 146 by long; however, the ITSI of M. laxa differed at three positions from the ITSI of M. fructicola. Although the sequences of the ITS1 regions from both species were nearly identical, the enzyme tilrel cuts the PCR-amplified ITSI region of the two species differentially. PCR amplification of the 3′ end of the SSU rRNA gene yielded products of approximately 940 and 520 by from M. fructicola and M. laxa, respectively. A 421-bp group I intron was detected by PCR within the SSU rDNA of 32 isolates of M. fructicola but not in the eight isolates of M. laxa. Intron sequences from each of four isolates of M. fructicola were identical, and the SSU rDNA flanking sequenc...