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Planarian cell number depends on blitzschnell, a novel gene family that balances cell proliferation and cell death

机译:平面依赖于Blitzschnell,这是一种结合细胞增殖和细胞死亡的新型基因系列

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摘要

Control of cell number is crucial to define body size during animal development and to restrict tumoral transformation. The cell number is determined by the balance between cell proliferation and cell death. Although many genes are known to regulate those processes, the molecular mechanisms underlying the relationship between cell number and body size remain poorly understood. This relationship can be better understood by studying planarians, flatworms that continuously change their body size according to nutrient availability. We identified a novel gene family, blitzschnell (bls), that consists of de novo and taxonomically restricted genes that control cell proliferation:cell death ratio. Their silencing promotes faster regeneration and increases cell number during homeostasis. Importantly, this increase in cell number leads to an increase in body size only in a nutrient-rich environment; in starved planarians, silencing results in a decrease in cell size and cell accumulation that ultimately produces overgrowths. bls expression is downregulated after feeding and is related to activity of the insulin/Akt/mTOR network, suggesting that the bls family evolved in planarians as an additional mechanism for restricting cell number in nutrient-fluctuating environments.
机译:控制细胞数对于在动物发育期间限制体尺寸并限制肿瘤转化是至关重要的。细胞数由细胞增殖和细胞死亡之间的平衡决定。虽然已知许多基因调节这些过程,但细胞数和体型之间关系的分子机制仍然明白很差。通过研究平面图,可以更好地理解这种关系,根据营养可用性连续改变身体大小的扁平虫。我们鉴定了一种新型基因家族,闪电料(BLS),包括控制细胞增殖的De Novo和分类学限制基因:细胞死亡率。他们的沉默促进更快的再生,并在稳态期间增加细胞数。重要的是,细胞数的增加导致体尺寸的增加仅在富含营养的环境中;在饥饿的平面图中,沉默导致细胞大小和细胞积累的降低,最终产生过度生长。喂食后BLS表达被下调,并且相关的胰岛素/ AKT / mTOR的网络的活动,这表明BLS家族在涡演变为用于限制营养波动环境细胞数目的其他机制。

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