Department of Biological Sciences, University of New Hampshire, Durham, NH 03824, USA.
BMC Plant Biol. 2011 Nov 10;11:157. doi: 10.1186/1471-2229-11-157.
The genus Fragaria comprises species at ploidy levels ranging from diploid (2n = 2x = 14) to decaploid (2n = 10x = 70). Fluorescence in situ hybridization with 5S and 25S rDNA probes was performed to gather cytogenetic information that illuminates genomic divergence among different taxa at multiple ploidy levels, as well as to explore the evolution of ribosomal RNA genes during polyploidization in Fragaria.
Root tip cells of diploid taxa were typified by two 5S and six 25S rDNA hybridization signals of varying intensities, providing a baseline for comparisons within the genus. In three exceptional diploid genotypes, F. nilgerrensis (CFRA 1358 and CFRA 1825) and F. vesca 'Yellow Wonder', two 5S but only four 25S rDNA sites were found but with differing site losses. The numbers of 5S and 25S rDNA signals, respectively were three and nine in a triploid F. ×bifera accession, and were four and twelve in three tetraploids, thus occurring in proportional 1.5× and 2× multiples of the typical diploid pattern. In hexaploid F. moschata, a proportional multiple of six 5S rDNA sites was observed, but the number of 25S rDNA sites was one or two less than the proportionate prediction of eighteen. This apparent tendency toward rDNA site loss at higher ploidy was markedly expanded in octoploids, which displayed only two 5S and ten 25S rDNA sites. In the two decaploids examined, the numbers of 5S and 25S rDNA signals, respectively, were four and fifteen in F. virginiana subsp. platypetala, and six and twelve in F. iturupensis.
Among diploid Fragaria species, a general consistency of rDNA site numbers implies conserved genomic organization, but highly variable 25S signal sizes and intensities and two instances of site loss suggest concurrent high dynamics of rDNA copy numbers among both homologs and non-homologs. General conservation of rDNA site numbers in lower ploidy, but marked site number reductions at higher ploidy levels, suggest complex evolution of rDNA sites during polyploidization and/or independent evolutionary pathways for 6x versus higher ploidy strawberries. Site number comparisons suggest common genomic composition among natural octoploids, and independent origins of the two divergent decaploid accessions.
草莓属植物的物种具有从二倍体(2n = 2x = 14)到十倍体(2n = 10x = 70)的不同倍性水平。使用 5S 和 25S rDNA 探针的荧光原位杂交获得了细胞遗传学信息,这些信息阐明了不同倍性水平的不同分类群之间的基因组差异,并探讨了草莓属中核糖体 RNA 基因在多倍化过程中的进化。
二倍体分类群的根尖细胞表现出两个 5S 和六个不同强度的 25S rDNA 杂交信号,为属内比较提供了基线。在三个异常的二倍体基因型中,弗吉尼亚草莓(CFRA 1358 和 CFRA 1825)和黄草莓 'Yellow Wonder',发现了两个 5S 但只有四个 25S rDNA 位点,但有不同的缺失。三倍体 F. ×bifera 中的 5S 和 25S rDNA 信号数分别为三个和九个,四个四倍体中的 5S 和 25S rDNA 信号数分别为四个和十二个,因此分别以典型二倍体模式的 1.5×和 2×倍数出现。在六倍体 F. moschata 中,观察到六个 5S rDNA 位点的比例倍数,但 25S rDNA 位点的数量比预期的十八个少一或两个。这种在较高倍性下 rDNA 位点缺失的明显趋势在八倍体中明显扩大,八倍体仅显示两个 5S 和十个 25S rDNA 位点。在所检查的两个十倍体中,弗吉尼亚草莓亚种。platypetala 的 5S 和 25S rDNA 信号数分别为四个和十五个,而 F. iturupensis 的 5S 和 25S rDNA 信号数分别为六个和十二个。
在二倍体草莓属植物中,rDNA 位点数量的普遍一致性意味着基因组组织的保守性,但 25S 信号大小和强度的高度可变性以及两个位点缺失的实例表明,同源和非同源之间 rDNA 拷贝数的同时高度动态性。较低倍性中 rDNA 位点数量的普遍保守性,但在较高倍性水平上的显著位点减少表明 rDNA 位点在多倍化过程中的复杂进化,或 6x 与更高倍性草莓的独立进化途径。位点数量比较表明自然八倍体之间具有共同的基因组组成,并且两个不同的十倍体供体具有独立的起源。