Jones Rhian, Wijesinghe Susanne, Wilson Claire, Halsall John, Liloglou Triantafillos, Kanhere Aditi
School of Biosciences, University of Birmingham, Edgbaston, Birmingham, UK.
Institute of Inflammation and Ageing, University of Birmingham, Edgbaston, Birmingham, UK.
iScience. 2021 Mar 5;24(4):102273. doi: 10.1016/j.isci.2021.102273. eCollection 2021 Apr 23.
DNA methyl transferase-1 or DNMT1 maintains DNA methylation in the genome and is important for regulating gene expression in cells. Aberrant changes in DNMT1 activity and DNA methylation are commonly observed in cancers and many other diseases. Recently, a number of long intergenic non-protein-coding RNAs or lincRNAs have been shown to play a role in regulating DNMT1 activity. is a nuclear lincRNA that is frequently mutated in cancers and is a hotbed for disease-associated single nucleotide changes. However, the functional mechanism of is not understood. Here, we show that this lincRNA is concentrated on the nuclear periphery. Strikingly, in the absence of lincRNA, DNMT1 is mis-located in the cytoplasm, and the genomic DNA is significantly hypomethylated. This is accompanied by double-stranded DNA breaks and increased cell death. These results point to a previously unrecognized mechanism of lincRNA-mediated subcellular localization of DNMT1 and regulation of DNA methylation.
DNA甲基转移酶-1(DNMT1)维持基因组中的DNA甲基化,对调节细胞中的基因表达很重要。DNMT1活性和DNA甲基化的异常变化在癌症和许多其他疾病中普遍存在。最近,一些长链基因间非编码RNA(lincRNA)已被证明在调节DNMT1活性中发挥作用。[具体名称缺失]是一种在癌症中经常发生突变的核lincRNA,是疾病相关单核苷酸变化的温床。然而,[具体名称缺失]的功能机制尚不清楚。在这里,我们表明这种lincRNA集中在核周边。引人注目的是,在没有lincRNA的情况下,DNMT1错定在细胞质中,基因组DNA显著低甲基化。这伴随着双链DNA断裂和细胞死亡增加。这些结果指向了一种以前未被认识的lincRNA介导的DNMT1亚细胞定位和DNA甲基化调节机制。