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An approach to delineate primers for a group of poorly conserved sequences incorporating the common motif region

机译:描绘掺有共同基序区的一组保守性差的序列的引物的方法

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摘要

Glutathione synthetase (gshB) has previously been reported to confer tolerance to acidic soil condition in Rhizobium species. Cloning the gene coding for this enzyme necessitates the designing of proper primer sets which in turn depends on the identification of high quality sequence similarity in multiple global alignments. In this experiment, a group of homologous gene sequences related to gshB gene (accession no: gi-86355669:327589-328536) of Rhizobium etli CFN 42, were extracted from NCBI nucleotide sequence databases using BLASTN and were analyzed for designing degenerate primers. However, the T-coffee multiple global alignment results did not show any block of conserved region for the above sequence set to design the primers. Therefore, we attempted to identify the location of common motif region based on multiple local alignments employing the MEME algorithm supported with MAST and Primer3. The results revealed some common motif regions that enabled us to design the primer sets for related gshB gene sequences. The result will be validated in wet lab.
机译:以前已经报道谷胱甘肽合成酶(gshB)赋予根瘤菌属物种对酸性土壤条件的耐受性。克隆编码该酶的基因需要设计适当的引物,这又取决于在多个全局比对中鉴定高质量序列相似性。在该实验中,使用BLASTN从NCBI核苷酸序列数据库中提取与根瘤菌CFN 42的gshB基因(登录号:gi-86355669:327589-328536)有关的一组同源基因序列,并进行分析以设计简并引物。然而,对于上述设计引物的序列,T-咖啡多重整体比对结果没有显示任何保守区域的区段。因此,我们尝试使用MAST和Primer3支持的MEME算法,基于多个局部比对来识别共有基序区域的位置。结果揭示了一些常见的基序区域,使我们能够设计相关gshB基因序列的引物组。结果将在湿实验室中验证。

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