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用 ADAADi 改变哺乳动物转录网络:一种 ATP 依赖的染色质重塑抑制剂。

Altering mammalian transcription networking with ADAADi: An inhibitor of ATP-dependent chromatin remodeling.

机构信息

Chromatin Remodeling Laboratory, School of Life Sciences, JNU, New Delhi, India.

Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia, United States of America.

出版信息

PLoS One. 2021 May 17;16(5):e0251354. doi: 10.1371/journal.pone.0251354. eCollection 2021.

Abstract

Active DNA-dependent ATPase A Domain inhibitor (ADAADi) is the only known inhibitor of ATP-dependent chromatin remodeling proteins that targets the ATPase domain of these proteins. The molecule is synthesized by aminoglycoside phosphotransferase enzyme in the presence of aminoglycosides. ADAADi interacts with ATP-dependent chromatin remodeling proteins through motif Ia present in the conserved helicase domain, and thus, can potentially inhibit all members of this family of proteins. We show that mammalian cells are sensitive to ADAADi but with variable responses in different cell lines. ADAADi can be generated from a wide variety of aminoglycosides; however, cells showed differential response to ADAADi generated from various aminoglycosides. Using HeLa and DU145 cells as model system we have explored the effect of ADAADi on cellular functions. We show that the transcriptional network of a cell type is altered when treated with sub-lethal concentration of ADAADi. Although ADAADi has no known effects on DNA chemical and structural integrity, expression of DNA-damage response genes was altered. The transcripts encoding for the pro-apoptotic proteins were found to be upregulated while the anti-apoptotic genes were found to be downregulated. This was accompanied by increased apoptosis leading us to hypothesize that the ADAADi treatment promotes apoptotic-type of cell death by upregulating the transcription of pro-apoptotic genes. ADAADi also inhibited migration of cells as well as their colony forming ability leading us to conclude that the compound has effective anti-tumor properties.

摘要

活性依赖 DNA 的 ATP 酶 A 结构域抑制剂(ADAADi)是唯一已知的靶向这些蛋白质的 ATP 酶结构域的 ATP 依赖性染色质重塑蛋白抑制剂。该分子是在氨基糖苷类存在的情况下由氨基糖苷磷酸转移酶酶合成的。ADAADi 通过在保守的解旋酶结构域中存在的基序 Ia 与 ATP 依赖性染色质重塑蛋白相互作用,因此,可能抑制该蛋白家族的所有成员。我们表明哺乳动物细胞对 ADAADi 敏感,但在不同细胞系中反应不同。ADAADi 可以由多种氨基糖苷类药物产生;然而,细胞对不同氨基糖苷类药物产生的 ADAADi 表现出不同的反应。我们使用 HeLa 和 DU145 细胞作为模型系统,研究了 ADAADi 对细胞功能的影响。我们表明,当用亚致死浓度的 ADAADi 处理时,细胞的转录网络会发生改变。尽管 ADAADi 对 DNA 的化学和结构完整性没有已知的影响,但 DNA 损伤反应基因的表达发生了改变。发现编码促凋亡蛋白的转录物上调,而抗凋亡基因下调。这伴随着凋亡的增加,使我们假设 ADAADi 处理通过上调促凋亡基因的转录来促进凋亡型细胞死亡。ADAADi 还抑制细胞迁移和集落形成能力,使我们得出结论,该化合物具有有效的抗肿瘤特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f436/8128233/cfab791fcb73/pone.0251354.g001.jpg

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