CAS Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization &Ecological Restoration and Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, P.O. Box 416, Chengdu, Sichuan 610041, China.
Department of Biological Sciences, Inha University, Incheon 402-751, Republic of Korea.
Sci Rep. 2017 Jan 4;7:40057. doi: 10.1038/srep40057.
The internal transcribed spacer (ITS) as one part of nuclear ribosomal DNA is one of the most extensively sequenced molecular markers in plant systematics. The ITS repeats generally exhibit high-level within-individual homogeneity, while relatively small-scale polymorphism of ITS copies within individuals has often been reported in literature. Here, we identified large-scale polymorphism of ITS copies within individuals in the legume genus Lespedeza (Fabaceae). Divergent paralogs of ITS sequences, including putative pseudogenes, recombinants, and multiple functional ITS copies were sometimes detected in the same individual. Thirty-seven ITS pseudogenes could be easily detected according to nucleotide changes in conserved 5.8S motives, the significantly lower GC contents in at least one of three regions, and the lost ability of 5.8S rDNA sequence to fold into a conserved secondary structure. The distribution patterns of the putative functional clones were highly different between the traditionally recognized two subgenera, suggesting different rates of concerted evolution in two subgenera which could be attributable to their different extents/frequencies of hybridization, confirmed by our analysis of the single-copy nuclear gene PGK. These findings have significant implications in using ITS marker for reconstructing phylogeny and studying hybridization.
内转录间隔区(ITS)作为核核糖体 DNA 的一部分,是植物系统发育中最广泛测序的分子标记之一。ITS 重复通常表现出个体内高水平的同质性,而个体内 ITS 拷贝的相对小规模多态性在文献中经常被报道。在这里,我们在豆科胡枝子属植物中发现了个体内 ITS 拷贝的大规模多态性。ITS 序列的分歧旁系同源物,包括可能的假基因、重组体和多个功能的 ITS 拷贝,有时在同一个体中被检测到。根据保守的 5.8S 动机中的核苷酸变化、至少三个区域中一个区域的 GC 含量显著降低以及失去 5.8S rDNA 序列折叠成保守二级结构的能力,很容易检测到 37 个 ITS 假基因。假定功能克隆的分布模式在传统上被识别的两个亚属之间差异很大,这表明两个亚属的协同进化速度不同,这可能归因于它们杂交的不同程度/频率,这一点得到了我们对单拷贝核基因 PGK 的分析的证实。这些发现对使用 ITS 标记重建系统发育和研究杂交具有重要意义。