The role of tRNA-derived small RNAs in aging

被引:3
|
作者
Ha, Seokjun G. [1 ]
Lee, Seung-Jae, V [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, KAIST Stem Cell Ctr, Daejeon 34141, South Korea
关键词
CANCER PROGRESSION; OXIDATIVE STRESS; DNA-DAMAGE; LONGEVITY; FRAGMENTS; APOPTOSIS; BIOGENESIS; MATURATION; CLEAVAGE;
D O I
10.5483/BMBRep.2022-0199
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
Aging is characterized by a gradual decline in biological func-tions, leading to the increased probability of diseases and deaths in organisms. Previous studies have identified biological factors that modulate aging and lifespan, including non-coding RNAs (ncRNAs). Here, we review the relationship between aging and tRNA-derived small RNAs (tsRNAs), ncRNAs that are generated from the cleavage of tRNAs. We describe age-dependent changes in tsRNA levels and their functions in age-related diseases, such as cancer and neurodegenerative diseases. We also discuss the association of tsRNAs with aging-regulating processes, including mitochondrial respiration and reduced mRNA translation. We cover recent findings regarding the potential roles of tsRNAs in cellular senescence, a major cause of organismal aging. Overall, our review will provide useful information for understanding the roles of tsRNAs in aging and age-associated diseases. [BMB Reports 2023; 56(2): 49-55]
引用
收藏
页码:49 / 55
页数:7
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