Contrasting expression patterns of coding and noncoding parts of the human genome upon oxidative stress

• Main Authors: Kuznetsov, Vladimir Andreevich, Vardy, Leah Anne, Ivshina, Anna Vladimirovna, Giannakakis, Antonis, Zhang, Jingxian, Jenjaroenpun, Piroon, Nama, Srikanth, Zainolabidin, Norliyana, Aau, Mei Yee, Yarmishyn, Aliaksandr A., Vaz, Candida, Grinchuk, Oleg V., Voorhoeve, Mathijs, Sampath, Prabha, Kurochkin, Igor V., Guccione, Ernesto
• Other Authors: School of Computer Engineering
• Format: Article
• Language: English
• Published: 2015
• Subjects: DRNTU::Science::Biological sciences::Genetics
• Online Access: https://hdl.handle.net/10356/105695; http://hdl.handle.net/10220/26058
• Institution: Nanyang Technological University

Oxidative stress (OS) is caused by an imbalance between pro- and anti-oxidant reactions leading to accumulation of reactive oxygen species within cells. We here investigate the effect of OS on the transcriptome of human fibroblasts. OS causes a rapid and transient global induction of transcription characterized by pausing of RNA polymerase II (PolII) in both directions, at specific promoters, within 30 minutes of the OS response. In contrast to protein-coding genes, which are commonly down-regulated, this novel divergent, PolII pausing-phenomenon leads to the generation of thousands of long noncoding RNAs (lncRNAs) with promoter-associated antisense lncRNAs transcripts (si-paancRNAs) representing the major group of stress-induced transcripts. OS causes transient dynamics of si-lncRNAs in nucleus and cytosol, leading to their accumulation at polysomes, in contrast to mRNAs, which get depleted from polysomes. We propose that si-lncRNAs represent a novel component of the transcriptional stress that is known to determine the outcome of immediate-early and later cellular stress responses and we provide insights on the fate of those novel mature lncRNA transcripts by showing that their association with polysomal complexes is significantly increased in OS.