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首页> 外文期刊>Journal of Microbiology, Biotechnology and Food Sciences >SEQUENCING OF FLAX LIS-1 INSERTION SITE IN THE ALBIDUM GENOTYPE
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SEQUENCING OF FLAX LIS-1 INSERTION SITE IN THE ALBIDUM GENOTYPE

机译:亚麻LIS-1插入位点在白头翁基因型中的序列

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The paper presents a methodology of identifying the insertion site of LIS-1-1 (Linum Insertion Sequence 1) element in flax Albidum variety when growing under the in vitro combined with environmental stress conditions. Abiotic stress was induced by a reduced nutrient content in a growth medium. The LIS-1 insertion site amplification was reaLIS-1ed using the forward LIS-L: 5'-GGG CAG TTT AAC TGT AAC GAA - 3 'and revers LIS-R: 5'-GCT TGG ATT TAG ACT TGG CAA C - 3' primers by PCR. PCR product was sequenced by direct sequencing method to proove the nucleotide sequence for matching with database LIS-1 sequence. A comparison has been matched with the sequence of the amplified segment in the database for all nucleotides except the 11-position in the 5'-3 ' direction, where instead of the three adenine pair is a couple in the Albidum variety. Changes caused by mobile elements or insertion sequences result in common flax in variability that can be used for the purposes of development of effective marker identification or environment based markers development.
机译:本文提出了一种在体外结合环境胁迫条件下生长时,鉴定亚麻Albidum品种中LIS-1-1(Linum插入序列1)元素的插入位点的方法。非生物胁迫是由于生长培养基中营养成分减少而引起的。使用正向LIS-L:5'-GGG CAG TTT AAC TGT AAC GAA-3'和反向LIS-R:5'-GCT TGG ATT TAG TAG CAA C-3重新增加LIS-1插入位点的扩增PCR引物。通过直接测序法对PCR产物进行测序,以证明与数据库LIS-1序列匹配的核苷酸序列。比较已与数据库中所有核苷酸的扩增片段的序列匹配,除了5'-3'方向上的11位以外,其中在Albidum品种中取代了三个腺嘌呤对。由可移动元素或插入序列引起的变化会导致常见的亚麻变异性,可用于开发有效的标记识别或基于环境的标记开发。

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