Lengerer Birgit, Wunderer Julia, Pjeta Robert, Carta Giada, Kao Damian, Aboobaker Aziz, Beisel Christian, Berezikov Eugene, Salvenmoser Willi, Ladurner Peter
Institute of Zoology and Center of Molecular Bioscience Innsbruck, University of Innsbruck, Technikerstr. 25, A-6020 Innsbruck, Austria.
Division of Physiology, Medical University of Innsbruck, Schöpfstraße 41/EG, A-6020 Innsbruck, Austria.
Dev Biol. 2018 Jan 15;433(2):448-460. doi: 10.1016/j.ydbio.2017.07.021. Epub 2017 Jul 28.
Temporal and spatial characterization of gene expression is a prerequisite for the understanding of cell-, tissue-, and organ-differentiation. In a multifaceted approach to investigate gene expression in the tail plate of the free-living marine flatworm Macrostomum lignano, we performed a posterior-region-specific in situ hybridization screen, RNA sequencing (RNA-seq) of regenerating animals, and functional analyses of selected tail-specific genes. The in situ screen revealed transcripts expressed in the antrum, cement glands, adhesive organs, prostate glands, rhabdite glands, and other tissues. Next we used RNA-seq to characterize temporal expression in the regenerating tail plate revealing a time restricted onset of both adhesive organs and copulatory apparatus regeneration. In addition, we identified three novel previously unannotated genes solely expressed in the regenerating stylet. RNA interference showed that these genes are required for the formation of not only the stylet but the whole male copulatory apparatus. RNAi treated animals lacked the stylet, vesicula granulorum, seminal vesicle, false seminal vesicle, and prostate glands, while the other tissues of the tail plate, such as adhesive organs regenerated normally. In summary, our findings provide a large resource of expression data during homeostasis and regeneration of the morphologically complex tail regeneration and pave the way for a better understanding of organogenesis in M. lignano.
基因表达的时空特征是理解细胞、组织和器官分化的先决条件。为了从多方面研究自由生活的海洋扁虫秀丽隐杆线虫尾板中的基因表达,我们进行了后区特异性原位杂交筛选、再生动物的RNA测序(RNA-seq)以及选定的尾部特异性基因的功能分析。原位筛选揭示了在窦、粘液腺、粘附器官、前列腺、杆状体腺和其他组织中表达的转录本。接下来,我们使用RNA-seq来表征再生尾板中的时间表达,揭示了粘附器官和交配器官再生的时间限制起始。此外,我们鉴定了三个仅在再生口针中表达的新的先前未注释的基因。RNA干扰表明,这些基因不仅是口针形成所必需的,而且是整个雄性交配器官形成所必需的。RNAi处理的动物缺乏口针、颗粒泡、精囊、假精囊和前列腺,而尾板的其他组织,如粘附器官正常再生。总之,我们的研究结果提供了形态复杂的尾部再生在稳态和再生过程中的大量表达数据资源,并为更好地理解秀丽隐杆线虫的器官发生铺平了道路。