DNA lesions that block transcription induce the death of Trypanosoma cruzi via ATR activation, which is dependent on the presence of R-loops

IF 3 3区 生物学 Q2 GENETICS & HEREDITY
Isabela Cecilia Mendes , Willian dos Reis Bertoldo , Adalberto Sales Miranda-Junior , Antônio Vinícius de Assis , Bruno Marçal Repolês , Wesley Roger Rodrigues Ferreira , Daniela Ferreira Chame , Daniela De Laet Souza , Raphael Souza Pavani , Andrea Mara Macedo , Glória Regina Franco , Esteban Serra , Virginia Perdomo , Carlos Frederico Martins Menck , Giovana da Silva Leandro , Stenio Perdigão Fragoso , Maria Carolina Quartim Barbosa Elias , Carlos Renato Machado
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引用次数: 0

Abstract

Trypanosoma cruzi is the etiological agent of Chagas disease and a peculiar eukaryote with unique biological characteristics. DNA damage can block RNA polymerase, activating transcription-coupled nucleotide excision repair (TC-NER), a DNA repair pathway specialized in lesions that compromise transcription. If transcriptional stress is unresolved, arrested RNA polymerase can activate programmed cell death. Nonetheless, how this parasite modulates these processes is unknown. Here, we demonstrate that T. cruzi cell death after UV irradiation, a genotoxic agent that generates lesions resolved by TC-NER, depends on active transcription and is signaled mainly by an apoptotic-like pathway. Pre-treated parasites with α-amanitin, a selective RNA polymerase II inhibitor, become resistant to such cell death. Similarly, the gamma pre-irradiated cells are more resistant to UV when the transcription processes are absent. The Cockayne Syndrome B protein (CSB) recognizes blocked RNA polymerase and can initiate TC-NER. Curiously, CSB overexpression increases parasites' cell death shortly after UV exposure. On the other hand, at the same time after irradiation, the single-knockout CSB cells show resistance to the same treatment. UV-induced fast death is signalized by the exposition of phosphatidylserine to the outer layer of the membrane, indicating a cell death mainly by an apoptotic-like pathway. Furthermore, such death is suppressed in WT parasites pre-treated with inhibitors of ataxia telangiectasia and Rad3-related (ATR), a key DDR kinase. Signaling for UV radiation death may be related to R-loops since the overexpression of genes associated with the resolution of these structures suppress it. Together, results suggest that transcription blockage triggered by UV radiation activates an ATR-dependent apoptosis-like mechanism in T. cruzi, with the participation of CSB protein in this process.

阻止转录的 DNA 损伤通过 ATR 激活诱导克氏锥虫死亡,而 ATR 激活取决于 R 环的存在
克鲁斯锥虫是南美锥虫病的病原体,也是一种具有独特生物特性的奇特真核生物。DNA 损伤会阻断 RNA 聚合酶,激活转录耦合核苷酸切除修复(TC-NER),这是一种专门针对损害转录的损伤的 DNA 修复途径。如果转录压力得不到解决,受阻的 RNA 聚合酶就会激活程序性细胞死亡。然而,这种寄生虫如何调节这些过程尚不清楚。在这里,我们证明了 T. cruzi 细胞在紫外线照射后的死亡依赖于活跃的转录,并主要通过类似凋亡的途径发出信号。用α-amanitin(一种选择性 RNA 聚合酶 II 抑制剂)预处理过的寄生虫会对这种细胞死亡产生抵抗力。同样,当转录过程缺失时,经γ预照射的细胞对紫外线的抵抗力更强。Cockayne 综合征 B 蛋白(CSB)能识别被阻断的 RNA 聚合酶,并能启动 TC-NER 。奇怪的是,CSB 过表达会增加寄生虫在紫外线照射后不久的细胞死亡。另一方面,在照射后的同一时间,单基因敲除的 CSB 细胞对同样的处理表现出抵抗力。紫外线诱导的快速死亡信号是磷脂酰丝氨酸暴露于细胞膜外层,这表明细胞死亡主要是通过类似凋亡的途径。此外,在使用共济失调毛细血管扩张和Rad3相关(ATR)抑制剂(一种关键的DDR激酶)预处理的WT寄生虫中,这种死亡被抑制。紫外线辐射死亡的信号传递可能与 R 环有关,因为与解决这些结构相关的基因的过度表达会抑制这种死亡。总之,研究结果表明,紫外线辐射引发的转录阻断激活了一种类似于 ATR 依赖性的克柔病毒凋亡机制,CSB 蛋白参与了这一过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
DNA Repair
DNA Repair 生物-毒理学
CiteScore
7.60
自引率
5.30%
发文量
91
审稿时长
59 days
期刊介绍: DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease. DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.
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