Tsuda Y, Nakao K, Ide Y, Tsumura Y
Program in Plant Ecology and Evolution, Department of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, Norbyvägen 18D, 75236, Uppsala, Sweden; Department of Forest Genetics, Forestry and Forest Products Research Institute (FFPRI), Matsunosato 1, Tsukuba, Ibaraki, 305-8687, Japan.
Mol Ecol. 2015 Apr;24(7):1403-18. doi: 10.1111/mec.13123. Epub 2015 Mar 23.
Conservation of the local genetic variation and evolutionary integrity of economically and ecologically important trees is a key aspect of studies involving forest genetics, and a population demographic history of the target species provides valuable information for this purpose. Here, the genetic structure of 48 populations of Betula maximowicziana was assessed using 12 expressed sequence tag-simple sequence repeat (EST-SSR) markers. Genetic diversity was lower in northern populations than southern ones and structure analysis revealed three groups: northern and southern clusters and an admixed group. Eleven more genomic-SSR loci were added and the demographic history of these three groups was inferred by approximate Bayesian computation (ABC). The ABC revealed that a simple split scenario was much more likely than isolation with admixture, suggesting that the admixture-like structure detected in this species was due to ancestral polymorphisms. The ABC analysis suggested that the population growth and divergence of the three groups occurred 96 800 (95% CI, 20 500-599 000) and 28 300 (95% CI, 8700-98 400) years ago, respectively. We need to be aware of several sources of uncertainty in the inference such as assumptions about the generation time, overlapping of generations, confidence intervals of the estimated parameters and the assumed model in the ABC. However, the results of the ABC together with the model-based maps of reconstructed past species distribution and palaeoecological data suggested that the modern genetic structure of B. maximowicziana originated prior to the last glacial maximum (LGM) and that some populations survived in the northern range even during the LGM.
保护具有经济和生态重要性的树木的本地遗传变异和进化完整性是森林遗传学研究的一个关键方面,而目标物种的种群 demographic 历史为此提供了有价值的信息。在此,使用12个表达序列标签 - 简单序列重复(EST - SSR)标记评估了48个毛赤杨种群的遗传结构。北方种群的遗传多样性低于南方种群,结构分析揭示了三个组:北方和南方聚类以及一个混合组。又添加了11个基因组SSR位点,并通过近似贝叶斯计算(ABC)推断这三个组的 demographic 历史。ABC分析表明,简单的分裂情景比隔离与混合更有可能,这表明在该物种中检测到的类似混合的结构是由于祖先多态性。ABC分析表明,这三个组的种群增长和分化分别发生在96800(95%置信区间,20500 - 599000)和28300(95%置信区间,8700 - 98400)年前。我们需要意识到推断中的几个不确定性来源,例如关于世代时间、世代重叠、估计参数的置信区间以及ABC中假设模型的假设。然而,ABC的结果连同基于模型重建的过去物种分布地图和古生态数据表明,毛赤杨的现代遗传结构起源于末次盛冰期(LGM)之前,并且即使在LGM期间,一些种群仍在北方范围内存活。