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Reduced RNA turnover as a driver of cellular senescence

Abstract : Accumulation of senescent cells is an important contributor to chronic inflammation upon aging. The inflammatory phenotype of senescent cells was previously shown to be driven by cytoplasmic DNA. Here, we propose that cytoplasmic double-stranded RNA has a similar effect. We find that several cell types driven into senescence by different routes share an accumulation of long promoter RNAs and 3′ gene extensions rich in retrotransposon sequences. Accordingly, these cells display increased expression of genes involved in response to double stranded RNA of viral origin downstream of the interferon pathway. The RNA accumulation is associated with evidence of reduced RNA turnover, including in some cases, reduced expression of RNA exosome subunits. Reciprocally, depletion of RNA exosome subunit EXOSC3 accelerated expression of multiple senescence markers. A senescence-like RNA accumulation was also observed in cells exposed to oxidative stress, an important trigger of cellular senescence. Altogether, we propose that in a subset of senescent cells, repeat-containing transcripts stabilized by oxidative stress or reduced RNA exosome activity participate in driving and maintaining the permanent inflammatory state characterizing cellular senescence.
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Contributor : Anne-Laure Noel Connect in order to contact the contributor
Submitted on : Tuesday, January 26, 2021 - 4:07:53 PM
Last modification on : Tuesday, September 28, 2021 - 5:15:45 PM


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Distributed under a Creative Commons Attribution 4.0 International License



Nowsheen Mullani, Yevheniia Porozan, Adèle Mangelinck, Christophe Rachez, Mickaël Costallat, et al.. Reduced RNA turnover as a driver of cellular senescence. Life Science Alliance, Life Science Alliance LLC, 2021, 4 (3), pp.e202000809. ⟨10.1101/800128⟩. ⟨hal-02324027v2⟩



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