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Fear-of-intimacy-mediated zinc transport controls the function of zinc-finger transcription factors involved in myogenesis

机译:恐惧的亲密介导的锌转运控制参与成肌的锌指转录因子的功能

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摘要

Zinc is a component of one-tenth of all human proteins. Its cellular concentration is tightly regulated because its dyshomeostasis has catastrophic health consequences. Two families of zinc transporters control zinc homeostasis in organisms, but there is little information about their specific developmental roles. We show that the ZIP transporter Fear-of-intimacy (Foi) is necessary for the formation of Drosophila muscles. In foi mutants, myoblasts segregate normally, but their specification is affected, leading to the formation of a misshapen muscle pattern and distorted midgut. The observed phenotypes could be ascribed to the inactivation of specific zincfinger transcription factors (ZFTFs), supporting the hypothesis that they are a consequence of intracellular depletion of zinc. Accordingly, foi phenotypes can be rescued by mesodermal expression of other ZIP members with similar subcellular localization. We propose that Foi acts mostly as a transporter to regulate zinc intracellular homeostasis, thereby impacting on the activity of ZFTFs that control specific developmental processes. Our results additionally suggest a possible explanation for the presence of large numbers of zinc transporters in organisms based on differences in ion transport specificity and/or degrees of activity among transporters.
机译:锌是所有人类蛋白质的十分之一。它的细胞浓度受到严格调节,因为它的动态平衡会给健康带来灾难性的后果。锌转运蛋白的两个家族控制着生物体内的锌稳态,但是关于它们的特定发育作用的信息很少。我们表明ZIP转运恐惧亲密性(Foi)是果蝇肌肉形成所必需的。在foi突变体中,成肌细胞正常分离,但其规格受到影响,导致形成畸形的肌肉图案和中肠变形。观察到的表型可以归因于特定的锌指转录因子(ZFTFs)的失活,支持这一假设,即它们是锌在细胞内耗竭的结果。因此,可以通过具有相似亚细胞定位的其他ZIP成员的中胚层表达来拯救foi表型。我们建议Foi主要充当调节锌细胞内稳态的转运蛋白,从而影响控制特定发育过程的ZFTF的活性。我们的研究结果还提出了一种可能的解释,即基于离子转运特异性和/或转运蛋白之间的活性程度差异,生物体内大量锌转运蛋白的存在。

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