Kurokochi Hiroyuki, Zhang Shijie, Takeuchi Yoshie, Tan Engkong, Asakawa Shuichi, Lian Chunlan
Asian Natural Environmental Science Center, the University of Tokyo, 1-1-8 Midori-cho, Nishitokyo, Tokyo 188-0002, Japan.
Nagano Prefectural College of Forestry, 4385-1 Shinkai, Kiso, Kiso-gun, Nagano 397-0002, Japan.
J Fungi (Basel). 2017 May 11;3(2):23. doi: 10.3390/jof3020023.
The annual yield of matsutake mushrooms () has consistently decreased in Japan over the past few decades. We used 15 polymorphic and codominant simple sequence repeat (SSR) markers, developed using next-generation sequencing, to carry out genetic analyses of 10 populations in Nagano, Japan. Using the SSRs, we identified 223 genotypes, none of which was observed in more than one population. The mean expected heterozygosity and standardized allelic richness values were 0.67 and 4.05, respectively. Many alleles appeared in only one of the 10 populations; 34 of these private alleles were detected with a mean number per population of 3.4. The fixation index () and standardized genetic differentiation (') values were 0.019 and 0.028, respectively. Analysis of molecular variance (AMOVA) showed that the contribution of among population, among genets within a population, and within genets variation to the total variation was 2.91%, 11.62%, and 85.47%, respectively, with genetic differentiation being detected for all sources. Twenty-eight of 45 pairwise values were significantly larger than zero, and no pattern of isolation by distance was detected among the 10 populations. Bayesian-based clustering did not show clear differences among populations. These results suggest that reestablishment of a colony would be best accomplished by transplantation within a field; if this is not possible, then transplantation from within several dozen kilometers will cause little damage to the original population genetic structure.
在过去几十年里,日本松茸的年产量持续下降。我们使用了15个多态性共显性简单序列重复(SSR)标记(通过下一代测序开发),对日本长野的10个种群进行了遗传分析。利用这些SSR标记,我们鉴定出223种基因型,没有一种在多个种群中被观察到。平均期望杂合度和标准化等位基因丰富度值分别为0.67和4.05。许多等位基因仅出现在10个种群中的一个;检测到34个这些私有等位基因,每个种群的平均数为3.4。固定指数()和标准化遗传分化(')值分别为0.019和0.028。分子方差分析(AMOVA)表明,种群间、种群内基因间以及基因内变异对总变异的贡献分别为2.91%、11.62%和85.47%,所有来源均检测到遗传分化。45对值中有28对显著大于零,10个种群之间未检测到距离隔离模式。基于贝叶斯的聚类在种群间未显示出明显差异。这些结果表明,通过在田间内移植来重新建立一个群体是最好的方法;如果这不可能,那么从几十公里范围内进行移植对原始种群遗传结构造成的损害很小。