Key Laboratory of Molecular Cytogenetics and Genetic Breeding, College of Life Science and Technology, Harbin Normal University, Harbin, 150025, Heilongjiang, People's Republic of China.
Plant Cell Rep. 2011 Dec;30(12):2207-13. doi: 10.1007/s00299-011-1126-7. Epub 2011 Jul 28.
A plant short interspersed element (SINE) was identified in Glycine max after re-sequencing of the soybean sequence characterized amplified region (SCAR) markers. Detailed analysis revealed that this newly recognized SINE element consisted of a tRNA-related region, a tRNA non-related region, direct flanking repeat sequences, and a short stretch of Ts at the 3'-terminal region. These features are similar to previously characterized SINEs. To investigate the evolution of the SINE retroposon, BLASTN was used to search against genome sequences of other plants. Since it is homologous with the retroposon Au in Aegilops umbellulata (wheat) and its homology in soybean, the SINE is named as GmAu1. Genome analysis of the Glycine max var. Willimas 82 uncovered more than 847 copies of GmAu1 per haploid genome of soybean. Examination of the regions flanking the inserted GmAu1 sequences indicated a preference for introns over exons or other noncoding regions. Considering the flanking insertion sequences, 146 primers were designed in order to detect insertion mutations by a PCR-based method. Seventy-seven primers displayed polymorphism and were used to develop corresponding GmAu1-based SCAR markers. The retroposon GmAu1 and its related SCAR markers identified in this study will prove valuable to future investigations into the genetic mapping, phylogeny, and evolution of the Glycine genus.
大豆序列特征扩增区域 (SCAR) 标记重测序后,在大豆中鉴定出一个短散布元件 (SINE)。详细分析表明,这个新识别的 SINE 元件由一个 tRNA 相关区域、一个 tRNA 非相关区域、直接侧翼重复序列和 3'末端区域的一小段 Ts 组成。这些特征与先前表征的 SINE 相似。为了研究 SINE 反转录转座子的进化,使用 BLASTN 对其他植物的基因组序列进行搜索。由于它与 Aegilops umbellulata(小麦)中的反转录转座子 Au 及其在大豆中的同源性,因此将 SINE 命名为 GmAu1。对 Glycine max var. Williams 82 的基因组分析发现,每个大豆单倍体基因组中含有超过 847 个 GmAu1 拷贝。对插入的 GmAu1 序列侧翼区域的检查表明,插入更倾向于内含子而不是外显子或其他非编码区域。考虑到侧翼插入序列,设计了 146 个引物,以便通过基于 PCR 的方法检测插入突变。77 个引物显示出多态性,并用于开发相应的基于 GmAu1 的 SCAR 标记。本研究中鉴定的反转录转座子 GmAu1 及其相关的 SCAR 标记将有助于未来对大豆属的遗传图谱、系统发育和进化的研究。