Malakar Pushkar
Department of Medical Biotechnology, School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute (RKMVERI), Kolkata, India.
Front Cell Dev Biol. 2024 Dec 23;12:1410308. doi: 10.3389/fcell.2024.1410308. eCollection 2024.
Long non-coding RNAs (lncRNAs) are a fascinating, but still largely uncharacterized, class of genes. Recently, lncRNAs have attracted significant attention due to their emerging functions in development and disease. The role of lncRNAs in chromosome instability or aneuploidy is not extensively studied.
We started with the objective of characterizing lncRNAs that play an important role in chromosome instability (CIN) or aneuploidy. Here, we report the initial functional characterization of PURPL in the context of chromosomal instability or aneuploidy.
We report the over-expression of lncRNA PURPL in three experimental models of chromosomal instability, or aneuploidy. In addition, the study also showed that the extent or magnitude of PURPL expression is dependent upon p53 status. Our research also showed that turning off PURPL is enough to create a CIN phenotype in RPE-1 cell lines that were previously karyotypically stable. Moreover, PURPL knockdown cells are more sensitive to CIN or aneuploidy inducers.
These findings show that PURPL is essential for maintaining chromosomal or genomic stability in mammalian cells. Collectively, the study demonstrated that lncRNA-PURPL significantly contributes to CIN, or aneuploidy.
长链非编码RNA(lncRNAs)是一类引人入胜但仍 largely uncharacterized 的基因。最近,lncRNAs因其在发育和疾病中的新功能而备受关注。lncRNAs在染色体不稳定或非整倍体中的作用尚未得到广泛研究。
我们从表征在染色体不稳定(CIN)或非整倍体中起重要作用的lncRNAs这一目标出发。在此,我们报告了PURPL在染色体不稳定或非整倍体背景下的初步功能表征。
我们报告了lncRNA PURPL在三种染色体不稳定或非整倍体实验模型中的过表达。此外,该研究还表明PURPL表达的程度或幅度取决于p53状态。我们的研究还表明,关闭PURPL足以在先前核型稳定的RPE-1细胞系中产生CIN表型。此外,PURPL敲低的细胞对CIN或非整倍体诱导剂更敏感。
这些发现表明PURPL对维持哺乳动物细胞中的染色体或基因组稳定性至关重要。总体而言,该研究表明lncRNA-PURPL对CIN或非整倍体有显著贡献。