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Identification of an AFLP molecular marker linked to parthenocarpy gene in monoecious cucumber.

机译:与雌雄同株单性结实基因连锁的AFLP分子标记的鉴定。

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In order to identify molecular markers linked to parthenocarpy in cucumber (Cucumis sativus L.), parthenocarpy and non-parthenocarpy DNA pools were created from F2 crosses between a highly parthenocarpic monoecious line '6457' and a non-parthenocarpic line '6429' according to the principle of bulk segregant analysis (BSA). The amplified fragment length polymorphism (AFLP) technique was employed with 256 primer combinations to detect the polymorphisms between the DNA pools. In total, 8544 scorable AFLP bands were generated, yielding an average of 33.38 fragments per primer combination. In the non-parthenocarpy DNA pool, a 325 bp specific fragment was amplified with the primer E41/M47, the band did not appear in the parthenocarpic pool. This marker, designated AGG/CAA325 was validated with DNA from the F2 population. Linkage analysis using MapMaker 3.0 indicated that the genetic distance from the marker to the non-parthenocarpy locus was 9.7 cM.
机译:为了鉴定与黄瓜( Cucumis sativus L.)单性结实有关的分子标记,从高度单性结实的雌雄同株的F 2 杂交中创建了单性结实和非无性结实的DNA库。根据批量分离分析(BSA)的原理,“ 6457”行和非果皮行“ 6429”行。扩增的片段长度多态性(AFLP)技术与256个引物组合一起用于检测DNA库之间的多态性。总共产生了8544条可评分的AFLP条带,每个引物组合平均产生33.38个片段。在非拟果皮DNA池中,用引物E41 / M47扩增了325 bp的特异片段,在单性结实池中未出现条带。该标记称为AGG / CAA 325 ,已通过F 2 群体的DNA进行了验证。使用MapMaker 3.0进行的连锁分析表明,从标记到非腮腺位点的遗传距离为9.7 cM。

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