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mRNA stability in response to m⁶A placement is linked to cell identity in planarians

Title data

Höhn, Constantin ; Pittroff, Andreas ; Gribling-Burrer, Anne-Sophie ; Hülsmann, Lisa ; Smyth, Redmond P. ; Kuhn, Claus-D.:
mRNA stability in response to m⁶A placement is linked to cell identity in planarians.
bioRxiv , 2026
DOI: https://doi.org/10.64898/2026.03.27.714417

Official URL: Volltext

Project information

Project title:
Project's official title
Project's id
Die Rolle von piRNAs und N6-Methyladenosin (m6A) in der Epidermis von Planarien
450313021
Genregulation durch nicht-kodierende RNA
450312765
Der Mechanismus der Aufhebung der Promoter-proximalen Pause von RNA-Polymerase II durch Enhancer RNAs
314375425

Project financing: Deutsche Forschungsgemeinschaft

Abstract in another language

N6-methyladenosine (m6A) is a prevalent internal modification of eukaryotic mRNA that influences transcript fate, including mRNA stability and cell-type-specific gene expression. However, the mechanisms underlying m6A-mediated regulation remain poorly understood in many systems, including the highly regenerative planarian Schmidtea mediterranea. To address this, we generated a high-confidence atlas of ~72,200 m6A sites across the planarian transcriptome using multiplexed direct RNA sequencing. The m6A sites follow a DRAYW consensus motif and are highly enriched near stop codons while being largely excluded from coding sequences. This pattern aligns with an exon length-dependent variant of the exon junction complex-mediated (EJC) exclusion model, wherein the EJC restricts m6A deposition near splice sites. Knockdown of the m6A writer complex induced pronounced, cell-type-specific changes in transcript stability. Destabilized transcripts were enriched for intestinal markers, whereas stabilized transcripts were associated with neoblasts, the adult stem cells of planarians. Transcriptional shut-off experiments further confirmed that m6A has opposing effects on mRNA decay depending on cellular context: it stabilizes transcripts in differentiated cells, while it promotes the degradation of mRNAs associated with neoblasts. Collectively, these results support a model in which cell-type-specific regulation of mRNA stability by m6A plays a crucial role in shaping cell identity in planarians.

Further data

Item Type: Preprint, postprint
Institutions of the University: Faculties
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair RNA Biochemistry
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair RNA Biochemistry > Chair RNA Biochemistry - Univ.-Prof. Dr. Claus-Dieter Kuhn
Profile Fields
Profile Fields > Advanced Fields
Profile Fields > Advanced Fields > Molecular Biosciences
Research Networks > Molecules, Life and AI
Research Institutions
Research Institutions > Central research institutes > Bayreuth Center for Molecular Biosciences - BZMB
Research Institutions > Central research institutes > Bayreuth Center of Ecology and Environmental Research- BayCEER
Research Institutions > Affiliated Institutes > Medizincampus Oberfranken (MCO)
Result of work at the UBT: Yes
DDC Subjects: 500 Science
500 Science > 500 Natural sciences
500 Science > 570 Life sciences, biology
Date Deposited: 08 Apr 2026 09:32
Last Modified: 08 Apr 2026 11:04
URI: https://eref.uni-bayreuth.de/id/eprint/96739