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表观转录组写入器 ALKBH8 可促进机体耐受性,并保护小鼠肺部免受环境污染物萘的伤害。

The epitranscriptomic writer ALKBH8 drives tolerance and protects mouse lungs from the environmental pollutant naphthalene.

机构信息

Department of Nanoscale Science and Engineering, University at Albany , Albany, NY, USA.

College of Pharmacy, Department of Toxicology and Pharmacology, University of Arizona , Tucson, AZ, USA.

出版信息

Epigenetics. 2020 Oct;15(10):1121-1138. doi: 10.1080/15592294.2020.1750213. Epub 2020 Apr 17.

DOI:10.1080/15592294.2020.1750213
PMID:32303148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7518688/
Abstract

The epitranscriptomic writer Alkylation Repair Homolog 8 (ALKBH8) is a transfer RNA (tRNA) methyltransferase that modifies the wobble uridine of selenocysteine tRNA to promote the specialized translation of selenoproteins. Using deficient ( mice, we have investigated the importance of epitranscriptomic systems in the response to naphthalene, an abundant polycyclic aromatic hydrocarbon and environmental toxicant. We performed basal lung analysis and naphthalene exposure studies using wild type (WT), and mice, the latter of which lack the cytochrome P450 enzymes required for naphthalene bioactivation. Under basal conditions, lungs from mice have increased markers of oxidative stress and decreased thioredoxin reductase protein levels, and have reprogrammed gene expression to differentially regulate stress response transcripts. mice are more sensitive to naphthalene induced death than WT, showing higher susceptibility to lung damage at the cellular and molecular levels. Further, WT mice develop a tolerance to naphthalene after 3 days, defined as resistance to a high challenging dose after repeated exposures, which is absent in mice. We conclude that the epitranscriptomic writer ALKBH8 plays a protective role against naphthalene-induced lung dysfunction and promotes naphthalene tolerance. Our work provides an early example of how epitranscriptomic systems can regulate the response to environmental stress .

摘要

表观转录writer 烷基化修复同源物 8 (ALKBH8) 是一种转移 RNA (tRNA) 甲基转移酶,可修饰硒代半胱氨酸 tRNA 的摆动尿嘧啶,以促进硒蛋白的特殊翻译。使用 缺陷型 (小鼠,我们研究了表观转录系统在应对萘(一种丰富的多环芳烃和环境毒物)中的重要性。我们使用野生型 (WT) 和 小鼠进行了基础肺分析和萘暴露研究,后者缺乏萘生物活化所需的细胞色素 P450 酶。在基础条件下, 小鼠的肺部有增加的氧化应激标志物和减少的硫氧还蛋白还原酶蛋白水平,并且重新编程基因表达以差异调节应激反应转录物。 小鼠比 WT 对萘诱导的死亡更敏感,在细胞和分子水平上表现出更高的肺损伤易感性。此外,WT 小鼠在 3 天后对萘产生了耐受性,定义为在重复暴露后对高挑战性剂量的抗性,而 小鼠则没有。我们得出结论,表观转录 writer ALKBH8 在对抗萘引起的肺功能障碍中起保护作用,并促进萘耐受。我们的工作提供了一个早期的例子,说明表观转录系统如何调节对环境应激的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/5be4b8f37c60/KEPI_A_1750213_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/5028ae3af626/KEPI_A_1750213_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/d6a0fb49e12a/KEPI_A_1750213_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/638b6fdb2372/KEPI_A_1750213_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/23a10371d216/KEPI_A_1750213_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/45d7633864cd/KEPI_A_1750213_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/47938ca24a87/KEPI_A_1750213_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/5be4b8f37c60/KEPI_A_1750213_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/5028ae3af626/KEPI_A_1750213_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/d6a0fb49e12a/KEPI_A_1750213_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/638b6fdb2372/KEPI_A_1750213_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/23a10371d216/KEPI_A_1750213_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/45d7633864cd/KEPI_A_1750213_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/47938ca24a87/KEPI_A_1750213_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7518688/5be4b8f37c60/KEPI_A_1750213_F0007_OC.jpg

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