Context-Dependent Function of Long Noncoding RNA PURPL in Transcriptome Regulation during p53 Activation.
Corrine Corrina R HartfordRoshan L ShresthaLorinc PongorYongmei ZhaoXiongfong ChenCaroline FromontRitu ChaudharyXiao Ling LiKatherine R PasterczykRavi KumarBruna R MuysDimitrios TsitsipatisRaj ChariMyriam GorospeMirit I AladjemJaved KhanMunira A BasraiIoannis GrammatikakisAshish LalPublished in: Molecular and cellular biology (2022)
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.
Keyphrases
- single cell
- rna seq
- cell cycle arrest
- genome wide
- poor prognosis
- long noncoding rna
- cell death
- induced apoptosis
- gene expression
- long non coding rna
- crispr cas
- air pollution
- dna methylation
- bioinformatics analysis
- mesenchymal stem cells
- machine learning
- deep learning
- cell therapy
- drug induced
- stress induced
- smoking cessation