Evidence map›Paper›PMID 39394354›Full record

ArticleThe EMBO journal2024

Modeling of mRNA deadenylation rates reveal a complex relationship between mRNA deadenylation and decay.

Agnieszka Czarnocka-Cieciura, Jarosław Poznański, Matti Turtola, Rafał Tomecki, Paweł S Krawczyk, Seweryn Mroczek, Wiktoria Orzeł, Upasana Saha, Torben Heick Jensen, Andrzej Dziembowski and 1 more

Abstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

11 authors.

Agnieszka Czarnocka-Cieciura *International Institute of Molecular and Cell Biology, Księcia Trojdena 4, 02-109, Warsaw, Poland.ORCID http://orcid.org/0000-0002-8088-5026
Jarosław Poznański *Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Adolfa Pawińskiego 5A, 02-106, Warsaw, Poland.ORCID http://orcid.org/0000-0003-2684-1775
Matti TurtolaDepartment of Life Technologies, University of Turku, Biocity, Tykistökatu 6, 205240, Turku, Finland.ORCID http://orcid.org/0000-0003-1694-1027
Rafał TomeckiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Adolfa Pawińskiego 5A, 02-106, Warsaw, Poland.
Paweł S KrawczykInternational Institute of Molecular and Cell Biology, Księcia Trojdena 4, 02-109, Warsaw, Poland.
Seweryn MroczekInternational Institute of Molecular and Cell Biology, Księcia Trojdena 4, 02-109, Warsaw, Poland.
Wiktoria OrzełInternational Institute of Molecular and Cell Biology, Księcia Trojdena 4, 02-109, Warsaw, Poland.ORCID http://orcid.org/0000-0003-2639-4944
Upasana SahaAarhus University, Department of Molecular Biology and Genetics-Universitetsbyen 81, 8000, Aarhus, Denmark.
Torben Heick JensenAarhus University, Department of Molecular Biology and Genetics-Universitetsbyen 81, 8000, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-5127-1239
Andrzej DziembowskiInternational Institute of Molecular and Cell Biology, Księcia Trojdena 4, 02-109, Warsaw, Poland. adziembowski@iimcb.gov.pl.ORCID http://orcid.org/0000-0001-8492-7572
Agnieszka TudekInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Adolfa Pawińskiego 5A, 02-106, Warsaw, Poland. atudek@ibb.waw.pl.ORCID http://orcid.org/0000-0002-6085-1072

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) 101097317European Molecular Biology Organization (EMBO) ALTF 328-2019Fundacja na rzecz Nauki Polskiej (FNP) TEAM/2016-1/3MNiSW | Narodowe Centrum Badań i Rozwoju (NCBR) LIDER/35/46/L-3/11/NCBR/2012Narodowe Centrum Nauki (NCN) 2017/26/E/NZ1/00724Narodowe Centrum Nauki (NCN) 2020/38/E/NZ2/00372Narodowe Centrum Nauki (NCN) 2020/39/D/NZ2/02174Research Council of Finland (AKA) 349698Research Council of Finland (AKA) 353682
6 · The paper itself

Abstract

Complete cytoplasmic polyadenosine tail (polyA-tail) deadenylation is thought to be essential for initiating mRNA decapping and subsequent degradation. To investigate this prevalent model, we conducted direct RNA sequencing of S. cerevisiae mRNAs derived from chase experiments under steady-state and stress condition. Subsequently, we developed a numerical model based on a modified gamma distribution function, which estimated the transcriptomic deadenylation rate at 10 A/min. A simplified independent method, based on the delineation of quantile polyA-tail values, showed a correlation between the decay and deadenylation rates of individual mRNAs, which appeared consistent within functional transcript groups and associated with codon optimality. Notably, these rates varied during the stress response. Detailed analysis of ribosomal protein-coding mRNAs (RPG mRNAs), constituting 40% of the transcriptome, singled out this transcript group. While deadenylation and decay of RPG mRNAs accelerated under heat stress, their degradation could proceed even when deadenylation was blocked, depending entirely on ongoing nuclear export. Our findings support the general primary function of deadenylation in dictating the onset of decapping, while also demonstrating complex relations between these processes.

Indexed as

RNA, MessengerRNA StabilitySaccharomyces cerevisiaePoly ARNA, FungalSaccharomyces cerevisiae ProteinsTranscriptomePoly ARNA, FungalRNA, MessengerSaccharomyces cerevisiae ProteinsCcr4-NOT and Pan2/3 DeadenylasesDcp2 Decapping and Xrn1 DegradationmRNA Deadenylation and DegradationONT Nanopore Direct RNA Sequencing (DRS)Pab1

Identifiers

PMID39394354
PMCPMC11649921

What OpenQuestion holds

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Registered trials

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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.