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Characterizing homologues of crop domestication genes in poorly described wild relatives by high‐throughput sequencing of whole genomes

机译:通过全基因组的高通量测序表征在野生亲属的作物驯化基因的同源物

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Wild crop relatives represent a source of novel alleles for crop genetic improvement. Screening biodiversity for useful or diverse gene homologues has often been based upon the amplification of targeted genes using available sequence information to design primers that amplify the target gene region across species. The crucial requirement of this approach is the presence of sequences with sufficient conservation across species to allow for the design of universal primers. This approach is often not successful with diverse organisms or highly variable genes. Massively parallel sequencing (MPS) can quickly produce large amounts of sequence data and provides a viable option for characterizing homologues of known genes in poorly described genomes. MPS of genomic DNA was used to obtain species-specific sequence information for 18 rice genes related to domestication characteristics in a wild relative of rice, Microlaena stipoides. Species-specific primers were available for 16 genes compared with 12 genes using the universal primer method. The use of species-specific primers had the potential to cover 92% of the sequence of these genes, while traditional universal primers could only be designed to cover 80%. A total of 24 species-specific primer pairs were used to amplify gene homologues, and 11 primer pairs were successful in capturing six gene homologues. The 23 million, 36-base pair (bp) paired end reads, equated to an average of 2X genome coverage, facilitated the successful amplification and sequencing of six target gene homologues, illustrating an important approach to the discovery of useful genes in wild crop relatives.
机译:野生作物亲属代表作物遗传改善的新等位基因来源。筛选用于有用或多种基因同源物的生物多样性通常基于使用可用的序列信息扩增靶向基因,以设计跨物种扩增靶基因区域的引物。这种方法的关键要求是存在具有足够保护的序列,以允许设计通用引物。这种方法通常不成功,不同的生物体或高度可变基因。大规模平行测序(MPS)可以快速产生大量的序列数据,并提供可行的选择,用于表征已知基因的同源物在较差的基因组中。基因组DNA的MPS用于获得与野生植物的野生相对的驯化特征有关的18种水稻基因的物种特异性序列信息。使用通用底漆法与12个基因相比,可获得16个基因的物种特异性引物。使用物种特异性引物的使用具有覆盖这些基因的92%的序列,而传统的通用引物只能设计成覆盖80%。总共24种特异性引物对扩增基因同源物,11引物对捕获六个基因同源物成功。 2300万,36碱基对(BP)成对的末端读数,等于2x基因组覆盖率,促进了六种靶基因同源物的成功扩增和测序,说明了在野生作物中发现有用基因的重要方法。

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