Munehara Hiroyuki, Horita Miho, Kimura-Kawaguchi Motoko R, Yamazaki Aya
Field Science Center for Northern Biosphere Hokkaido University Hakodate Hokkaido Japan.
Graduate School of Environmental Science Hokkaido University Hakodate Hokkaido Japan.
Ecol Evol. 2016 Sep 14;6(19):7126-7140. doi: 10.1002/ece3.2446. eCollection 2016 Oct.
Two natural, hemiclonal hybrid strains were discovered in three species. The natural hybrids, all of which were females that produced haploid eggs containing only the genome (maternal ancestor; hereafter ), generated F hybrid-type offspring by fertilization with haploid sperm of or (paternal species; and , respectively). This study was performed to clarify the extent of diversification between the two hybrids and the maternal ancestor. Genealogical analysis using mtDNA revealed that all 38 / hybrids formed a branch (Branch I) with 18 of the 33 / hybrids. No haplotype sharing was observed with the maternal ancestor. Further, microsatellite DNA analysis suggested that the members of Branch I shared the same hemiclonal genome set. The results suggested that / hybrids originated by anomalous hybridization, or "host switching," between / and , and not from interspecific hybridization between and . The remaining 9 of 11 / haplotypes and all of the 27 haplotypes were mixed within the genealogical tree, as if they had originated from multiple mutations. However, / could also mate with . Although offspring from this host switch (Backcross-) have the same genome as normal , a part of their genome retains genetic factors capable of producing hemiclones. Consequently, when a descendant of a BC- hybrid mates with males, a new hemiclone lineage will arise. Multiple haplotype revival through host switching from a single mutation in hybrids is another possible hypothesis for the observed mixing of / haplotypes within the mtDNA genealogical tree.
在三个物种中发现了两个天然的半克隆杂交菌株。这些天然杂交种均为雌性,它们产生仅含有基因组(母本祖先;以下简称 )的单倍体卵,通过与 或 的单倍体精子(父本物种;分别为 和 )受精产生F杂交型后代。本研究旨在阐明这两个杂交种与母本祖先之间的分化程度。使用线粒体DNA进行的系统发育分析表明,所有38个 / 杂交种与33个 / 杂交种中的18个形成了一个分支(分支I)。未观察到与母本祖先有单倍型共享。此外,微卫星DNA分析表明,分支I的成员共享相同的半克隆基因组集。结果表明, / 杂交种起源于 / 和 之间的异常杂交,即“宿主转换”,而非 和 之间的种间杂交。11个 / 单倍型中的其余9个以及所有27个 单倍型在系统发育树中混合在一起,就好像它们起源于多个突变。然而, / 也可以与 交配。尽管这种宿主转换(回交 - )产生的后代与正常 的基因组相同,但其基因组的一部分保留了能够产生半克隆的遗传因子。因此,当回交 - 杂交种的后代与 雄性交配时,将产生一个新的半克隆谱系。通过杂交种中的单个突变进行宿主转换导致多个单倍型复兴是线粒体DNA系统发育树中观察到的 / 单倍型混合的另一种可能假设。