Li Zhongwei, Wu Jinhua, Deleo Christopher J
Department of Biomedical Sciences, Florida Atlantic University, 777 Glades Road, Boca Raton, Florida 33431, USA.
IUBMB Life. 2006 Oct;58(10):581-8. doi: 10.1080/15216540600946456.
RNA damage has been recently reported to increase under oxidative stress and in patients with many degenerative diseases, which has drawn attention to the consequences of RNA oxidation at the molecular and cellular levels. Under similar conditions the levels of oxidative damage in RNA are usually higher than those in DNA, which may impair protein synthesis or other RNA function. Therefore, accumulation of RNA damage must be prevented and cells have developed specific mechanisms to remove oxidatively-damaged RNA and to block incorporation of oxidized nucleotides during RNA synthesis. Removal of oxidized RNA may be mediated by specific proteins that recognize oxidative lesions and direct the RNA degradation machinery to eliminate the damaged RNAs. During RNA synthesis, oxidized ribonucleotides are hydrolyzed or discriminated from normal ribonucleotides during transcription, preventing their incorporation into RNA. Collective evidence suggests that RNA oxidative damage is a challenging and persistent problem normally controlled through RNA surveillance mechanisms, making them critical to maintaining cellular health and preventing disease.
最近有报道称,在氧化应激条件下以及许多退行性疾病患者体内,RNA损伤会增加,这引起了人们对RNA氧化在分子和细胞水平上所产生后果的关注。在类似条件下,RNA中的氧化损伤水平通常高于DNA中的氧化损伤水平,这可能会损害蛋白质合成或其他RNA功能。因此,必须防止RNA损伤的积累,细胞已经发展出特定机制来去除氧化损伤的RNA,并在RNA合成过程中阻止氧化核苷酸的掺入。氧化RNA的去除可能由特定蛋白质介导,这些蛋白质识别氧化损伤并引导RNA降解机制消除受损的RNA。在RNA合成过程中,氧化核糖核苷酸在转录过程中会被水解或与正常核糖核苷酸区分开来,从而防止它们掺入RNA。综合证据表明,RNA氧化损伤是一个具有挑战性的持续性问题,通常通过RNA监测机制来控制,这使得这些机制对于维持细胞健康和预防疾病至关重要。