bioRxivCell BiologyPreprint
Aquarius RNA helicase Protects Pluripotent Stem Cell Identity
Maxime LalondeiD, Elizabeth Márquez-GómeziD, Clare S.K. LeeiD, Adam BurtoniD, Ioannis TsirkasiD, Fernanda Rezende Pabst, Marcel WerneriD, Atiqa Sajid, Augusto Chaves MurrielloiD, Xanthoula Karypidou, Andreas W. EttingeriD, Tamás SchaueriD, Tobias StraubiD, Maria‐Elena Torres‐PadillaiD, Antonio ScialdoneiD, Stephan HamperliD
Abstract
Pluripotent stem cells must reconcile rapid replication with a highly dynamic transcriptional program, creating an inherent susceptibility to transcription-replication conflicts (TRCs). We demonstrate that embryonic stem cells (ESCs) operate in a "resilient" replication mode, tolerating high genomic traffic through the constitutive upregulation of R-loop and TRC resolution pathways. Through a targeted functional screen, we identify the RNA helicase Aquarius (AQR) as an essential safeguard of this state. AQR depletion downregulates these resolution factors, collapsing this stress-resistant program and driving ESCs into unstable, heterogenous states, marked by increased transcriptional entropy and cell-to-cell noise. Mechanistically, we show that key identity-defining genes are preferentially located within R-loop and TRC prone regions, making them uniquely vulnerable to AQR depletion. Our findings establish AQR as a critical governor of transcriptional fidelity, demonstrating that genomic resilience is fundamental to maintaining pluripotent cell identity.
- organism: mouse
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: development & morphogenesis
- research focus: chromatin & epigenetic regulation
- approach: experimental assay
- Citations
- 0
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