Janssen Toon, Vizoso Dita B, Schulte Gregor, Littlewood D Timothy J, Waeschenbach Andrea, Schärer Lukas
Evolutionary Biology, Zoological Institute, University of Basel, Vesalgasse 1, 4051 Basel, Switzerland; Nematology Research Unit, Department of Biology, Ghent University, K.L. Ledeganckstraat 35, 9000 Ghent, Belgium.
Evolutionary Biology, Zoological Institute, University of Basel, Vesalgasse 1, 4051 Basel, Switzerland.
Mol Phylogenet Evol. 2015 Nov;92:82-107. doi: 10.1016/j.ympev.2015.06.004. Epub 2015 Jun 17.
The Macrostomorpha-an early branching and species-rich clade of free-living flatworms-is attracting interest because it contains Macrostomum lignano, a versatile model organism increasingly used in evolutionary, developmental, and molecular biology. We elucidate the macrostomorphan molecular phylogeny inferred from both nuclear (18S and 28S rDNA) and mitochondrial (16S rDNA and COI) marker genes from 40 representatives. Although our phylogeny does not recover the Macrostomorpha as a statistically supported monophyletic grouping, it (i) confirms many taxa previously proposed based on morphological evidence, (ii) permits the first placement of many families and genera, and (iii) reveals a number of unexpected placements. Specifically, Myozona and Bradynectes are outside the three classic families (Macrostomidae, Microstomidae and Dolichomacrostomidae) and the asexually fissioning Myomacrostomum belongs to a new subfamily, the Myozonariinae nov. subfam. (Dolichomacrostomidae), rather than diverging early. While this represents the first evidence for asexuality among the Dolichomacrostomidae, we show that fissioning also occurs in another Myozonariinae, Myozonaria fissipara nov. sp. Together with the placement of the (also fissioning) Microstomidae, namely as the sister taxon of Dolichomacrostomidae, this suggests that fissioning is not basal within the Macrostomorpha, but rather restricted to the new taxon Dolichomicrostomida (Dolichomacrostomidae+Microstomidae). Furthermore, our phylogeny allows new insights into the evolution of the reproductive system, as ancestral state reconstructions reveal convergent evolution of gonads, and male and female genitalia. Finally, the convergent evolution of sperm storage organs in the female genitalia appears to be linked to the widespread occurrence of hypodermic insemination among the Macrostomorpha.
大口涡虫纲是自由生活扁虫中一个早期分支且物种丰富的类群,正吸引着人们的关注,因为它包含了里氏大口涡虫(Macrostomum lignano),这是一种在进化生物学、发育生物学和分子生物学中越来越常用的多功能模式生物。我们从40个代表物种的核基因(18S和28S rDNA)和线粒体基因(16S rDNA和COI)推断出大口涡虫纲的分子系统发育。尽管我们的系统发育分析并未将大口涡虫纲作为一个得到统计学支持的单系类群恢复出来,但它(i)证实了许多先前基于形态学证据提出的分类单元,(ii)允许首次确定许多科和属的位置,并且(iii)揭示了一些意外的分类位置。具体而言,肌口区(Myozona)和缓游虫属(Bradynectes)位于三个经典科(大口涡虫科、微口涡虫科和长口大口涡虫科)之外,并且进行无性分裂的肌口大口涡虫属(Myomacrostomum)属于一个新亚科,即新肌口区亚科(Myozonariinae nov. subfam.)(长口大口涡虫科),而不是早期分化出来的。虽然这代表了长口大口涡虫科中无性生殖的首个证据,但我们表明分裂现象也发生在另一种新肌口区物种——裂殖肌口区虫(Myozonaria fissipara nov. sp.)中。连同(同样进行分裂的)微口涡虫科的位置,即作为长口大口涡虫科的姐妹分类单元,这表明分裂现象并非大口涡虫纲的基部特征,而是局限于新分类单元——多微口涡虫目(Dolichomicrostomida)(长口大口涡虫科 + 微口涡虫科)。此外,我们的系统发育分析使我们对生殖系统的进化有了新的认识,因为祖先状态重建揭示了性腺以及雄性和雌性生殖器的趋同进化。最后,雌性生殖器中精子储存器官的趋同进化似乎与大口涡虫纲中广泛存在的皮下受精现象有关。