Oxidative Stress, Transfer RNA Metabolism, and Protein Synthesis

被引:7
作者
Akiyama, Yasutoshi [1 ,5 ]
Ivanov, Pavel [2 ,3 ,4 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab Oncol Pharm Practice & Sci, Sendai, Japan
[2] Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, Boston, MA USA
[3] Harvard Med Sch, Dept Med, Boston, MA USA
[4] Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, 60 Fenwood Rd, Boston, MA 02115 USA
[5] Tohoku Univ, Lab Oncol Pharm Practice & Sci, Grad Sch Pharmaceut Sci, Sendai 9808578, Japan
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
tRNA; oxidative stress; protein synthesis; stress response; RNA; POLYMERASE-III TRANSCRIPTION; RIBONUCLEASE INHIBITOR; CANCER PROGRESSION; ARSENIC-BINDING; CYTOCHROME-C; ANGIOGENIN; TRANSLATION; FRAGMENTS; CELLS; METHYLATION;
D O I
10.1089/ars.2022.0206
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: Oxidative stress refers to excessive intracellular levels of reactive oxygen species (ROS) due to an imbalance between ROS production and the antioxidant defense system. Under oxidative stress conditions, cells trigger various stress response pathways to protect themselves, among which repression of messenger RNA (mRNA) translation is one of the key hallmarks promoting cell survival. This regulation process minimizes cellular energy consumption, enabling cells to survive in adverse conditions and to promote recovery from stress-induced damage.Recent Advances: Recent studies suggest that transfer RNAs (tRNAs) play important roles in regulating translation as a part of stress response under adverse conditions. In particular, research relying on high-throughput techniques such as next-generation sequencing and mass spectrometry approaches has given us detailed information on mechanisms such as individual tRNA dynamics and crosstalk among post-transcriptional modifications.Critical Issues: Oxidative stress leads to dynamic tRNA changes, including their localization, cleavage, and alteration of expression profiles and modification patterns. Growing evidence suggests that these changes not only are tightly regulated by stress response mechanisms, but also can directly fine-tune the translation efficiency, which contributes to cell- or tissue-specific response to oxidative stress.Future Directions: In this review, we describe recent advances in the understanding of the dynamic changes of tRNAs caused by oxidative stress. We also highlight the emerging roles of tRNAs in translation regulation under the condition of oxidative stress. In addition, we discuss future perspectives in this research field.
引用
收藏
页码:715 / 735
页数:21
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