Babben Steve, Perovic Dragan, Koch Michael, Ordon Frank
Julius Kühn-Institut (JKI), Federal Research Centre for Cultivated Plants, Institute for Resistance Research and Stress Tolerance, Quedlinburg, Sachsen-Anhalt, Germany.
Deutsche Saatveredelung AG (DSV), Lippstadt, Nordrhein-Westfalen, Germany.
PLoS One. 2015 Nov 13;10(11):e0142746. doi: 10.1371/journal.pone.0142746. eCollection 2015.
Recent declines in costs accelerated sequencing of many species with large genomes, including hexaploid wheat (Triticum aestivum L.). Although the draft sequence of bread wheat is known, it is still one of the major challenges to developlocus specific primers suitable to be used in marker assisted selection procedures, due to the high homology of the three genomes. In this study we describe an efficient approach for the development of locus specific primers comprising four steps, i.e. (i) identification of genomic and coding sequences (CDS) of candidate genes, (ii) intron- and exon-structure reconstruction, (iii) identification of wheat A, B and D sub-genome sequences and primer development based on sequence differences between the three sub-genomes, and (iv); testing of primers for functionality, correct size and localisation. This approach was applied to single, low and high copy genes involved in frost tolerance in wheat. In summary for 27 of these genes for which sequences were derived from Triticum aestivum, Triticum monococcum and Hordeum vulgare, a set of 119 primer pairs was developed and after testing on Nulli-tetrasomic (NT) lines, a set of 65 primer pairs (54.6%), corresponding to 19 candidate genes, turned out to be specific. Out of these a set of 35 fragments was selected for validation via Sanger's amplicon re-sequencing. All fragments, with the exception of one, could be assigned to the original reference sequence. The approach presented here showed a much higher specificity in primer development in comparison to techniques used so far in bread wheat and can be applied to other polyploid species with a known draft sequence.
近期成本的下降加速了对许多大基因组物种的测序,包括六倍体小麦(普通小麦Triticum aestivum L.)。尽管面包小麦的草图序列已为人所知,但由于三个基因组的高度同源性,开发适用于标记辅助选择程序的位点特异性引物仍是主要挑战之一。在本研究中,我们描述了一种开发位点特异性引物的有效方法,该方法包括四个步骤,即:(i)鉴定候选基因的基因组和编码序列(CDS);(ii)内含子和外显子结构重建;(iii)鉴定小麦A、B和D亚基因组序列,并根据三个亚基因组之间的序列差异开发引物;(iv)测试引物的功能、正确大小和定位。该方法应用于参与小麦抗冻性的单拷贝、低拷贝和高拷贝基因。总之,对于其中27个从普通小麦、一粒小麦和大麦中获得序列的基因,开发了一组119对引物,在缺体-四体(NT)系上进行测试后,一组65对引物(54.6%),对应19个候选基因,结果证明具有特异性。其中选择了一组35个片段通过桑格扩增子重测序进行验证。除一个片段外,所有片段都可与原始参考序列匹配。与目前在面包小麦中使用的技术相比,本文提出的方法在引物开发中显示出更高的特异性,并且可应用于具有已知草图序列的其他多倍体物种。