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The ATM- and ATR-related SCD domain is over-represented in proteins involved in nervous system development

机译:与ATM和ATR相关的SCD域在参与神经系统发育的蛋白质中过分表达

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摘要

ATM and ATR are cellular kinases with a well-characterized role in the DNA-damage response. Although the complete set of ATM/ATR targets is unknown, they often contain clusters of S/TQ motifs that constitute an SCD domain. In this study, we identified putative ATM/ATR targets that have a conserved SCD domain across vertebrates. Using this approach, we have identified novel putative ATM/ATR targets in pathways known to be under direct control of these kinases. Our analysis has also unveiled significant enrichment of SCD-containing proteins in cellular pathways, such as vesicle trafficking and actin cytoskeleton, where a regulating role for ATM/ATR is either unknown or poorly understood, hinting at a much broader and overarching role for these kinases in the cell. Of particular note is the overrepresentation of conserved SCD-containing proteins involved in pathways related to neural development. This finding suggests that ATM/ATR could be directly involved in controlling this process, which may be linked to the adverse neurological effects observed in patients with mutations in ATM.
机译:ATM和ATR是细胞激酶,在DNA损伤反应中具有很好的作用。尽管不知道完整的ATM / ATR目标集,但它们通常包含构成SCD域的S / TQ基序簇。在这项研究中,我们确定了在整个脊椎动物中具有保守SCD域的推定ATM / ATR目标。使用这种方法,我们在已知受这些激酶直接控制的途径中确定了新型推定的ATM / ATR目标。我们的分析还揭示了细胞途径中含有SCD的蛋白质的大量富集,例如囊泡运输和肌动蛋白细胞骨架,其中对ATM / ATR的调节作用尚不清楚或了解甚少,表明这些激酶的作用更为广泛和重要在牢房里特别值得注意的是参与神经发育相关途径的保守的含SCD的蛋白质的过度表达。这一发现表明,ATM / ATR可以直接参与控制这一过程,这可能与在ATM突变患者中观察到的不良神经系统作用有关。

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