Graduate School of Human and Environmental Studies, Kyoto University, Yoshida Nihonmatsu-cho, Sakyoku, Kyoto 606-8501, Japan.
Graduate School of Human and Environmental Studies, Kyoto University, Yoshida Nihonmatsu-cho, Sakyoku, Kyoto 606-8501, Japan.
Mol Phylogenet Evol. 2014 Oct;79:231-9. doi: 10.1016/j.ympev.2014.06.019. Epub 2014 Jun 27.
Prior studies of mitochondrial genomic variation reveal that the Japanese brown frog Rana tagoi comprises a complex of cryptic species lineages, and that R. sakuraii arose from within this complex. Neither species forms a monophyletic group on the mitochondrial haplotype tree, precluding a simple explanation for the evolutionary origins of R. sakuraii. We present a more complete sampling of mitochondrial haplotypic variation (from the ND1 and 16S genes) plus DNA sequence variation for five nuclear loci (from the genes encoding NCX1, NFIA, POMC, SLC8A3, and TYR) to resolve the evolutionary histories of these species. We test hypotheses of population assignment (STRUCTURE) and isolation-with-migration (IM) using the more slowly evolving nuclear markers. These demographic analyses of nuclear genetic variation confirm species-level distinctness and integrity of R. sakuraii despite its apparent polyphyly on the mitochondrial haplotype tree. Divergence-time estimates from both the mitochondrial haplotypes and nuclear genomic markers suggest that R. sakuraii originated approximately one million years ago, and that incomplete sorting of mitochondrial haplotype lineages best explains non-monophyly of R. sakuraii mitochondrial haplotypes. Cytonuclear discordance elsewhere in R. tagoi reveals a case of mitochondrial introgression between two species lineages on Honshu. The earliest phylogenetic divergence within this species group occurred approximately four million years ago, followed by cladogenetic events in the Pliocene and early Pleistocene yielding 10-13 extant species lineages, including R. sakuraii as one of the youngest.
先前对线粒体基因组变异的研究表明,日本林蛙 Rana tagoi 由一个隐种谱系的复杂群体组成,而 R. sakuraii 则是从这个复杂群体中产生的。这两个物种在线粒体单倍型树上都没有形成单系群,因此无法简单解释 R. sakuraii 的进化起源。我们提出了更完整的线粒体单倍型变异(来自 ND1 和 16S 基因)和五个核基因座的 DNA 序列变异(来自编码 NCX1、NFIA、POMC、SLC8A3 和 TYR 的基因),以解决这些物种的进化历史。我们使用进化较慢的核标记来测试种群分配(STRUCTURE)和隔离与迁移(IM)的假设。这些核遗传变异的人口分析确认了 R. sakuraii 的物种水平独特性和完整性,尽管其在线粒体单倍型树上明显为多系。来自线粒体单倍型和核基因组标记的分歧时间估计表明,R. sakuraii 起源于大约一百万年前,而线粒体单倍型谱系的不完全分类最佳解释了 R. sakuraii 线粒体单倍型的非单系性。R. tagoi 中的其他核质不和谐揭示了两个种系在本州之间发生线粒体渗入的情况。该物种组内最早的系统发育分歧发生在大约四百万年前,随后在上新世和早更新世发生了分支事件,产生了 10-13 个现存的种系,包括 R. sakuraii 作为最年轻的一个。