Schinkel Christoph C F, Kirchheimer Bernhard, Dullinger Stefan, Geelen Danny, De Storme Nico, Hörandl Elvira
Department of Systematics, Biodiversity and Evolution of Plants (with Herbarium), University of Goettingen, Untere Karspüle 2, 37073 Göttingen, Germany.
Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, 1030 Vienna, Austria.
Plant Syst Evol. 2017;303(8):1093-1108. doi: 10.1007/s00606-017-1435-6. Epub 2017 Jul 6.
Polyploidy is one of the most important evolutionary processes in plants. In natural populations, polyploids usually emerge from unreduced gametes which either fuse with reduced ones, resulting in triploid offspring (triploid bridge), or with other unreduced gametes, resulting in tetraploid embryos. The frequencies of these two pathways, and male versus female gamete contributions, however, are largely unexplored. occurs with diploid, triploid and autotetraploid cytotypes in the Alps, whereby diploids are mostly sexual, while tetraploids are facultative apomicts. To test for the occurrence of polyploidization events by triploid bridge, we investigated 551 plants of natural populations via flow cytometric seed screening. We assessed ploidy shifts in the embryo to reconstruct female versus male gamete contributions to polyploid embryo and/or endosperm formation. Seed formation via unreduced egg cells (B hybrids) occurred in all three cytotypes, while only in one case both gametes were unreduced. Polyploids further formed seeds with reduced, unfertilized egg cells (polyhaploids and aneuploids). Pollen was highly variable in diameter, but only pollen >27 μm was viable, whereby diploids produced higher proportions of well-developed pollen. Pollen size was not informative for the formation of unreduced pollen. These results suggest that a female triploid bridge via unreduced egg cells is the major pathway toward polyploidization in , maybe as a consequence of constraints of endosperm development. Triploids resulting from unreduced male gametes were not observed, which explains the lack of obligate sexual tetraploid individuals and populations. Unreduced egg cell formation in diploids represents the first step toward apomixis.
多倍体是植物中最重要的进化过程之一。在自然种群中,多倍体通常源自未减数配子,这些未减数配子要么与减数配子融合,产生三倍体后代(三倍体桥),要么与其他未减数配子融合,产生四倍体胚胎。然而,这两种途径的频率以及雄配子与雌配子的贡献在很大程度上尚未得到充分研究。在阿尔卑斯山,二倍体、三倍体和同源四倍体细胞型均有出现,其中二倍体大多为有性生殖,而四倍体为兼性无融合生殖。为了检测三倍体桥引发的多倍体化事件的发生情况,我们通过流式细胞术种子筛选对551株自然种群的植物进行了研究。我们评估了胚胎中的倍性变化,以重建雌配子与雄配子对多倍体胚胎和/或胚乳形成的贡献。通过未减数卵细胞形成种子(B杂交种)在所有三种细胞型中均有发生,而只有一例中两个配子均为未减数的。多倍体还通过减数的、未受精的卵细胞形成种子(多单倍体和非整倍体)。花粉直径变化很大,但只有直径大于27μm的花粉是有活力的,二倍体产生的发育良好的花粉比例更高。花粉大小对于未减数花粉的形成并无指示作用。这些结果表明,通过未减数卵细胞形成的雌三倍体桥是该植物多倍体化的主要途径,这可能是胚乳发育受限的结果。未观察到由未减数雄配子产生的三倍体,这解释了为何不存在专性有性四倍体个体和种群。二倍体中未减数卵细胞的形成代表了走向无融合生殖的第一步。