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A Synthetic DNA-Binding Domain Guides Distinct Chromatin-Modifying Small Molecules to Activate an Identical Gene Network

机译:合成的DNA结合域指导不同的染色质修饰小分子激活相同的基因网络。

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Synthetic dual-function ligands targeting specific DNA sequences and histone-modifying enzymes were applied to achieve regulatory control over multi-gene networks in living cells. Unlike the broad array of targeting small molecules for histone deacetylases (HDACs), few modulators are known for histone acetyltransferases (HATs), which play a central role in transcriptional control. As a novel chemical approach to induce selective HAT-regulated genes, we conjugated a DNA-binding domain (DBD) I to N-(4-chloro-3-trifluoromethyl-phenyl)-2-ethoxy-benzamide (CTB), an artificial HAT activator. Invitro enzyme activity assays and microarray studies were used to demonstrate that distinct functional small molecules could be transformed to have identical bioactivity when conjugated with a targeting DBD. This proof-of-concept synthetic strategy validates the switchable functions of HDACs and HATs in gene regulation and provides a molecular basis for developing versatile bioactive ligands.
机译:靶向特定DNA序列和组蛋白修饰酶的合成双功能配体被用于实现对活细胞中多基因网络的调控。与针对组蛋白脱乙酰基酶(HDAC)的多种靶向小分子不同,针对组蛋白乙酰基转移酶(HATs)的调节剂鲜为人知,后者在转录控制中起着核心作用。作为诱导选择性HAT调控基因的新型化学方法,我们将DNA结合结构域(DBD)I与人工合成的N-(4-氯-3-三氟甲基-苯基)-2-乙氧基苯甲酰胺(CTB)偶联HAT激活剂。体外酶活性测定和微阵列研究用于证明与靶向DBD偶联时,不同功能的小分子可以转化为具有相同的生物活性。这种概念验证的合成策略验证了HDAC和HAT在基因调控中的可转换功能,并为开发通用的生物活性配体提供了分子基础。

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