Monden Yuki, Yamamoto Ayaka, Shindo Akiko, Tahara Makoto
Graduate School of Environmental and Life Science, Okayama University, 1-1-1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
Faculty of Agriculture, Okayama University, 1-1-1 Tsushima-Naka, Kita-ku, Okayama 700-8530, Japan.
DNA Res. 2014 Oct;21(5):491-8. doi: 10.1093/dnares/dsu015. Epub 2014 Jun 16.
In many crop species, DNA fingerprinting is required for the precise identification of cultivars to protect the rights of breeders. Many families of retrotransposons have multiple copies throughout the eukaryotic genome and their integrated copies are inherited genetically. Thus, their insertion polymorphisms among cultivars are useful for DNA fingerprinting. In this study, we conducted a DNA fingerprinting based on the insertion polymorphisms of active retrotransposon families (Rtsp-1 and LIb) in sweet potato. Using 38 cultivars, we identified 2,024 insertion sites in the two families with an Illumina MiSeq sequencing platform. Of these insertion sites, 91.4% appeared to be polymorphic among the cultivars and 376 cultivar-specific insertion sites were identified, which were converted directly into cultivar-specific sequence-characterized amplified region (SCAR) markers. A phylogenetic tree was constructed using these insertion sites, which corresponded well with known pedigree information, thereby indicating their suitability for genetic diversity studies. Thus, the genome-wide comparative analysis of active retrotransposon insertion sites using the bench-top MiSeq sequencing platform is highly effective for DNA fingerprinting without any requirement for whole genome sequence information. This approach may facilitate the development of practical polymerase chain reaction-based cultivar diagnostic system and could also be applied to the determination of genetic relationships.
在许多作物品种中,需要进行DNA指纹识别以精确鉴定品种,从而保护育种者的权益。许多逆转录转座子家族在真核生物基因组中具有多个拷贝,并且它们的整合拷贝是可遗传的。因此,它们在品种间的插入多态性可用于DNA指纹识别。在本研究中,我们基于甘薯中活跃逆转录转座子家族(Rtsp-1和LIb)的插入多态性进行了DNA指纹识别。利用38个品种,我们通过Illumina MiSeq测序平台在这两个家族中鉴定出2024个插入位点。在这些插入位点中,91.4%在品种间似乎具有多态性,并且鉴定出376个品种特异性插入位点,这些位点被直接转化为品种特异性序列特征扩增区域(SCAR)标记。利用这些插入位点构建了系统发育树,其与已知的系谱信息高度吻合,从而表明它们适用于遗传多样性研究。因此,使用台式MiSeq测序平台对活跃逆转录转座子插入位点进行全基因组比较分析对于DNA指纹识别非常有效,且无需任何全基因组序列信息。这种方法可能有助于开发基于聚合酶链反应的实用品种诊断系统,也可应用于遗传关系的确定。