Evidence map›Paper›PMID 41484129›Full record

ArticleNature communications2026

Mechanistic insights into recruitment and regulation of the RNA helicase UPF1 in replication-dependent histone mRNA decay.

Alexandrina Machado de Amorim, Guangpu Xue, Wenxia He, Theresa Dittmers, Sarah Lewandowski, Cecilia Perez-Borrajero, Juliane Bethmann, Nevena Mateva, Clemens Krage, Vidhyadhar Nandana and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Alexandrina Machado de Amorim *Institute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Guangpu Xue *Institute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Wenxia HeIntegrated Program for Biological and Genome Sciences, University of North Carolina, Chapel Hill, NC, USA.ORCID http://orcid.org/0009-0008-9486-9386
Theresa DittmersInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0009-0002-7127-4976
Sarah LewandowskiInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0009-0006-6577-5597
Cecilia Perez-BorrajeroMolecular Systems Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID http://orcid.org/0000-0002-3167-7159
Juliane BethmannResearch Group Bioanalytical Mass Spectrometry, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Nevena MatevaInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Clemens KrageInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Vidhyadhar NandanaInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0003-0564-8343
Bernhard LollInstitute of Chemistry and Biochemistry, Laboratory of Structural Biochemistry, Freie Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0001-7928-4488
Tarek HilalInstitute of Chemistry and Biochemistry, Laboratory of Structural Biochemistry, Freie Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-7833-8058
Janosch HennigMolecular Systems Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID http://orcid.org/0000-0001-5214-7002
Henning UrlaubResearch Group Bioanalytical Mass Spectrometry, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.ORCID http://orcid.org/0000-0003-1837-5233
William F MarzluffIntegrated Program for Biological and Genome Sciences, University of North Carolina, Chapel Hill, NC, USA.ORCID http://orcid.org/0000-0003-3635-4073
Sutapa ChakrabartiInstitute of Chemistry and Biochemistry, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany. chakraba@zedat.fu-berlin.de.ORCID http://orcid.org/0000-0002-9877-173X

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) CH1245/3-2Deutsche Forschungsgemeinschaft (German Research Foundation) CH1245/5-1Deutsche Forschungsgemeinschaft (German Research Foundation) CH1245/6-1
6 · The paper itself

Abstract

Metazoan histone mRNAs are a unique class of mRNAs that lack the poly(A) tail present in all other eukaryotic transcripts. Instead, they end in a conserved stem-loop (SL) structure, necessitating a decay mechanism that is distinct from deadenylation-initiated degradation. Here, combining structural and functional approaches, we elucidate molecular mechanisms of initiation of histone mRNA decay. At the end of S-phase, the RNA helicase UPF1, the exoribonuclease 3'hExo and stem-loop binding protein SLBP all contribute to histone mRNA degradation, although how they are mechanistically coupled remained unknown. The cryoEM structure of an UPF1:SL RNA complex, presented here, shows that binding of UPF1 partially melts the RNA stem in the absence of ATP, harnessing the free energy derived from RNA-binding to unwind RNA. This melting event primes the SL-RNA for decay by 3'hExo. Using biochemical and cellular analyses, we demonstrate that SLBP directly engages the UPF1 helicase core to attenuate its unwinding activity and prevent premature degradation. Activation of UPF1 at a later stage promotes SL-RNA decay. We provide direct evidence that UPF1, SLBP and 3'hExo form a degradosome-like assembly that functionally couples SL unwinding and degradation, highlighting a dynamic and intricate network of UPF1-centric interactions that orchestrates timely histone mRNA decay.

Indexed as

HistonesRNA HelicasesRNA, MessengerRNA StabilityTrans-ActivatorsCryoelectron MicroscopyHeLa CellsHumansmRNA Cleavage and Polyadenylation FactorsNuclear ProteinsNucleic Acid ConformationProtein BindingHistonesmRNA Cleavage and Polyadenylation FactorsNuclear ProteinsRNA HelicasesRNA, MessengerSLBP protein, humanTrans-ActivatorsUPF1 protein, human

Identifiers

PMID41484129
PMCPMC12775136

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.