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A Comparative Transcriptomic Analysis Reveals Conserved Features of Stem Cell Pluripotency in Planarians and Mammals

机译:比较转录组分析揭示了平面图和哺乳动物中干细胞多能性的保守特征

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摘要

Many long-lived species of animals require the function of adult stem cells throughout their lives. However, the transcriptomes of stem cells in invertebrates and vertebrates have not been compared, and consequently, ancestral regulatory circuits that control stem cell populations remain poorly defined. In this study, we have used data from high-throughput RNA sequencing to compare the transcriptomes of pluripotent adult stem cells from planarians with the transcriptomes of human and mouse pluripotent embryonic stem cells. From a stringently defined set of 4,432 orthologs shared between planarians, mice and humans, we identified 123 conserved genes that are ≥5-fold differentially expressed in stem cells from all three species. Guided by this gene set, we used RNAi screening in adult planarians to discover novel stem cell regulators, which we found to affect the stem cell-associated functions of tissue homeostasis, regeneration, and stem cell maintenance. Examples of genes that disrupted these processes included the orthologs of TBL3, PSD12, TTC27, and RACK1. From these analyses, we concluded that by comparing stem cell transcriptomes from diverse species, it is possible to uncover conserved factors that function in stem cell biology. These results provide insights into which genes comprised the ancestral circuitry underlying the control of stem cell self-renewal and pluripotency.
机译:许多长寿命的动物一生都需要成年干细胞的功能。但是,没有对无脊椎动物和脊椎动物中干细胞的转录组进行比较,因此,控制干细胞种群的祖先调控电路仍然定义不清。在这项研究中,我们使用了来自高通量RNA测序的数据,将来自涡虫的多能成年干细胞的转录组与人和小鼠多能胚胎干细胞的转录组进行了比较。通过严格定义的一组4,432个直系同源物,在涡虫,小鼠和人类之间共享,我们鉴定了123个保守基因,在所有这三种物种的干细胞中差异表达≥5倍。以此基因集为指导,我们在成年涡虫中进行了RNAi筛选,发现了新的干细胞调节剂,我们发现它可以影响与组织稳态,再生和干细胞维持相关的干细胞相关功能。破坏这些过程的基因的例子包括TBL3,PSD12,TTC27和RACK1的直系同源基因。从这些分析中,我们得出结论,通过比较不同物种的干细胞转录组,有可能发现在干细胞生物学中起作用的保守因子。这些结果提供了关于哪些基因构成干细胞自我更新和多能性控制基础的祖先电路的见解。

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