长链非编码RNA PURPL在p53激活过程中转录组调控中的上下文依赖功能

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Corrine Corrina R Hartford, Roshan L Shrestha, Lorinc Pongor, Yongmei Zhao, Xiongfong Chen, Caroline Fromont, Ritu Chaudhary, Xiao Ling Li, Katherine R Pasterczyk, Ravi Kumar, Bruna R Muys, Dimitrios Tsitsipatis, Raj Chari, Myriam Gorospe, Mirit I Aladjem, Javed Khan, Munira A Basrai, Ioannis Grammatikakis, Ashish Lal
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引用次数: 2

摘要

PURPL是一种p53诱导的lncRNA,可抑制p53的基础水平。在这里,我们研究了肝癌细胞中p53激活时的PURPL,它的表达水平明显高于其他细胞类型。使用同种异构体测序,我们发现新的PURPL转录本具有保留的内含子和/或以前未注释的外显子。为了确定p53激活时PURPL的功能,我们在使用CRISPR干扰(CRISPRi)耗尽PURPL后进行转录组测序(RNA-Seq),然后用Nutlin处理诱导p53。引人注目的是,尽管在未经处理的细胞中PURPL的缺失只改变了7个基因的表达,但在p53激活时,PURPL的缺失导致了约800个基因的表达改变,揭示了PURPL的上下文依赖功能。通路分析表明,PURPL对于微调有丝分裂所需的特定基因的表达很重要。与这些结果一致,我们观察到PURPL耗竭后有丝分裂细胞的百分比显著下降。总的来说,这些数据确定了来自PURPL位点的新转录本,并表明PURPL在p53激活的背景下微妙地调节有丝分裂基因的表达,以控制细胞周期停滞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Context-Dependent Function of Long Noncoding RNA PURPL in Transcriptome Regulation during p53 Activation.

PURPL is a p53-induced lncRNA that suppresses basal p53 levels. Here, we investigated PURPL upon p53 activation in liver cancer cells, where it is expressed at significantly higher levels than other cell types. Using isoform sequencing, we discovered novel PURPL transcripts that have a retained intron and/or previously unannotated exons. To determine PURPL function upon p53 activation, we performed transcriptome sequencing (RNA-Seq) after depleting PURPL using CRISPR interference (CRISPRi), followed by Nutlin treatment to induce p53. Strikingly, although loss of PURPL in untreated cells altered the expression of only 7 genes, loss of PURPL resulted in altered expression of ~800 genes upon p53 activation, revealing a context-dependent function of PURPL. Pathway analysis suggested that PURPL is important for fine-tuning the expression of specific genes required for mitosis. Consistent with these results, we observed a significant decrease in the percentage of mitotic cells upon PURPL depletion. Collectively, these data identify novel transcripts from the PURPL locus and suggest that PURPL delicately moderates the expression of mitotic genes in the context of p53 activation to control cell cycle arrest.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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