N6-甲基腺苷
基因敲除
甲基化
RNA甲基化
生物
信使核糖核酸
核糖核酸
甲基转移酶
小RNA
滋养层
免疫沉淀
DNA甲基化
细胞生物学
分子生物学
化学
基因表达
基因
胎盘
生物化学
遗传学
胎儿
怀孕
作者
Yonggang Zhang,Hongling Yang,Yan Long,Yipeng Zhang,Ronggui Chen,Junzhu Shi,Jiying Chen
标识
DOI:10.1038/s41598-021-03662-5
摘要
Here, we performed N6-methyladenosine (m6A) RNA sequencing to determine the circRNA m6A methylation changes in the placentas during the pathogenesis of preeclampsia (PE). We verified the expression of the circRNA circPAPPA2 using quantitative reverse transcription-PCR. An invasion assay was carried out to identify the role of circPAPPA2 in the development of PE. Mechanistically, we investigated the cause of the altered m6A modification of circPAPPA2 through overexpression and knockdown cell experiments, RNA immunoprecipitation, fluorescence in situ hybridization and RNA stability experiments. We found that increases in m6A-modified circRNAs are prevalent in PE placentas and that the main changes in methylation occur in the 3'UTR and near the start codon, implicating the involvement of these changes in PE development. We also found that the levels of circPAPPA2 are decreased but that m6A modification is augmented. Furthermore, we discovered that methyltransferase‑like 14 (METTL14) increases the level of circPAPPA2 m6A methylation and that insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3) maintains circPAPPA2 stability. Decreases in IGF2BP3 levels lead to declines in circPAPPA2 levels. In summary, we provide a new vision and strategy for the study of PE pathology and report that placental circRNA m6A modification appears to be an important regulatory mechanism.
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