脱甲基酶
转录组
N6-甲基腺苷
RNA甲基化
黑磷
生物
核糖核酸
细胞生物学
化学
基因表达
DNA
基因
表观遗传学
甲基转移酶
甲基化
遗传学
材料科学
光电子学
作者
Fengkai Ruan,Jie Zeng,Hanying Yin,Shengwei Jiang,Xisen Cao,Naying Zheng,Changshun Han,Chuchu Zhang,Zhenghong Zuo,Chengyong He
标识
DOI:10.1002/smtd.202001045
摘要
Abstract Nanosafety is a major concern for nanotechnology development. Evaluation of the transcriptome and the DNA methylome is proposed for nanosafety assessments. RNA m6A modification plays a crucial role in development, disease, and cell fate determination through regulating RNA stability and decay. Here, since black phosphorus quantum dots (BPQDs), among many other types of QDs, increase the global m6A level and decrease the demethylase ALKBH5 level in lung cells, the epitranscriptome is taken into consideration for the first time to evaluate nanosafety. Both the transcriptome and m6A epitranscriptome analyses show that BPQDs alter many biological processes, such as the response to selenium ions and the lipoxygenase pathway, indicating possible ferroptosis activation. The results further show that BPQDs cause lipid peroxidation, mitochondrial dysfunction, and iron overload. Recognition of these modified mRNAs by YTHDF2 leads to mRNAs’ decay and eventually ferroptosis. This study shows that RNA m6A modification not only is a more sophisticated indicator for nanosafety assessment but also provides novel insight into the role of RNA m6A in regulating BPQD‐induced ferroptosis, which may be broadly applicable to understanding the functions of RNA m6A under stress.
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