Salina Elena A, Lim K Yoong, Badaeva Ekaterina D, Shcherban Andrey B, Adonina Irina G, Amosova Alexandra V, Samatadze Tatiana E, Vatolina Tatyana Yu, Zoshchuk Sviatoslav A, Leitch Andrew R
Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.
Genome. 2006 Aug;49(8):1023-35. doi: 10.1139/g06-050.
The evolution of 2 tandemly repeated sequences Spelt1 and Spelt52 was studied in Triticum species representing 2 evolutionary lineages of wheat and in Aegilops sect. Sitopsis, putative donors of their B/G genomes. Using fluorescence in situ hybridization we observed considerable polymorphisms in the hybridization patterns of Spelt1 and Spelt52 repeats between and within Triticum and Aegilops species. Between 2 and 28 subtelomeric sites of Spelt1 probe were detected in Ae. speltoidies, depending on accession. From 8 to 12 Spelt1 subtelomeric sites were observed in species of Timopheevi group (GAt genome), whereas the number of signals in emmer/aestivum accessions was significantly less (from 0 to 6). Hybridization patterns of Spelt52 in Ae. speltoides, Ae. longissima, and Ae. sharonensis were species specific. Subtelomeric sites of Spelt52 repeat were detected only in T. araraticum (T. timopheevii), and their number and chromosomal location varied between accessions. Superimposing copy number data onto our phylogenetic scheme constructed from RAPD data suggests 2 major independent amplifications of Spelt52 and 1 of Spelt1 repeats in Aegilops divergence. It is likely that the Spelt1 amplification took place in the ancient Ae. speltoides before the divergence of polyploid wheats. The Spelt52 repeat was probably amplified in the lineage of Ae. speltoides prior to divergence of the allopolyploid T. timopheevii but after the divergence of T. durum. In a separate amplification event, Spelt52 copy number expanded in the common ancestor of Ae. longissima and Ae. sharonensis.
在代表小麦两个进化谱系的小麦物种以及山羊草属拟斯卑尔脱山羊草组(其B/G基因组的假定供体)中,研究了两个串联重复序列Spelt1和Spelt52的进化。使用荧光原位杂交技术,我们观察到在小麦和山羊草物种之间以及物种内部,Spelt1和Spelt52重复序列的杂交模式存在相当大的多态性。在拟斯卑尔脱山羊草中,根据材料不同,检测到Spelt1探针的2至28个亚端粒位点。在提莫菲维组(GAt基因组)的物种中观察到8至12个Spelt1亚端粒位点,而在二粒小麦/普通小麦材料中的信号数量明显较少(0至6个)。Spelt52在拟斯卑尔脱山羊草、长穗山羊草和沙伦山羊草中的杂交模式具有物种特异性。Spelt重复序列的亚端粒位点仅在阿拉拉特小麦(提莫菲维小麦)中检测到,其数量和染色体位置在不同材料之间有所变化。将拷贝数数据叠加到我们根据RAPD数据构建的系统发育图谱上,表明在山羊草分化过程中,Spelt52有两次主要的独立扩增,Spelt1重复序列有一次扩增。Spelt1的扩增可能发生在古老的拟斯卑尔脱山羊草中,早于多倍体小麦的分化。Spelt52重复序列可能在异源多倍体提莫菲维小麦分化之前,但在硬粒小麦分化之后,在拟斯卑尔脱山羊草谱系中扩增。在一次单独的扩增事件中,Spelt52的拷贝数在长穗山羊草和沙伦山羊草的共同祖先中增加。