Kameoka Shinichiro, Sakio Hitoshi, Abe Harue, Ikeda Hajime, Setoguchi Hiroaki
Dept of Biology, Graduate School of Human and Environmental Studies, Kyoto University, Yoshida, Nihonmatsu-cho, Sakyoku, Kyoto, 606-8501, Japan.
Sado Station, Field center for sustainable agriculture and forestry, Faculty of agriculture, Niigata University, 94-2 Koda, Sado, Niigata, 952-2206, Japan.
J Plant Res. 2017 Mar;130(2):263-271. doi: 10.1007/s10265-016-0893-1. Epub 2016 Dec 21.
How phenotypic or genetic diversity is maintained in a natural habitat is a fundamental question in evolutionary biology. Flower color polymorphism in plants is a common polymorphism. Hepatica nobilis var. japonica on the Sea of Japan (SJ) side of the Japanese mainland exhibits within population flower color polymorphism (e.g., white, pink, and purple), while only white flowers are observed on the Pacific Ocean (PO) side. To determine the relationships between flower color polymorphism, within and among populations, and the genetic structure of H. nobilis var. japonica, we estimated the genetic variation using simple sequence repeat (SSR) markers. First, we examined whether cryptic lineages corresponding to distinct flower colors contribute to the flower color polymorphisms in H. nobilis var. japonica. In our field observations, no bias in color frequency was observed among populations on Sado Island, a region with high variation in flower color. Simple sequence repeat (SSR) analyses revealed that 18% of the genetic variance was explained by differences among populations, whereas no genetic variation was explained by flower color hue or intensity (0% for both components). These results indicate that the flower color polymorphism is likely not explained by cryptic lineages that have different flower colors. In contrast, populations in the SJ and PO regions were genetically distinguishable. As with the other plant species in these regions, refugial isolation and subsequent migration history may have caused the genetic structure as well as the spatially heterogeneous patterns of flower color polymorphisms in H. nobilis var. japonica.
在自然栖息地中,表型或遗传多样性是如何维持的,这是进化生物学中的一个基本问题。植物的花色多态性是一种常见的多态性。日本本州岛日本海一侧的獐耳细辛日本变种在种群内部表现出花色多态性(如白色、粉色和紫色),而在太平洋一侧只观察到白色花朵。为了确定獐耳细辛日本变种的花色多态性、种群内部和种群之间的关系以及遗传结构,我们使用简单序列重复(SSR)标记估计了遗传变异。首先,我们研究了与不同花色相对应的隐秘谱系是否对獐耳细辛日本变种的花色多态性有贡献。在我们的实地观察中,在花色变化较大的佐渡岛的种群中,未观察到颜色频率偏差。简单序列重复(SSR)分析表明,18%的遗传变异可由种群间差异解释,而花色色调或强度未解释任何遗传变异(两者均为零)。这些结果表明,花色多态性可能无法由具有不同花色的隐秘谱系来解释。相反,日本海和太平洋地区的种群在遗传上是可区分的。与这些地区的其他植物物种一样,避难所隔离和随后的迁移历史可能导致了獐耳细辛日本变种的遗传结构以及花色多态性的空间异质模式。