Evidence map›Paper›PMID 38589534›Full record

ArticleNature cell biology2024

Transcription bodies regulate gene expression by sequestering CDK9.

Martino Ugolini, Maciej A Kerlin, Ksenia Kuznetsova, Haruka Oda, Hiroshi Kimura, Nadine L Vastenhouw

Open access · hybridAbstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Metabolic labeling of RNA using ribonucleoside analogs enables the evaluation of RNA synthesis and degradation rates.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
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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

6 authors at 3 institutions in 4 countries.

Martino UgoliniCenter for Integrative Genomics (CIG), University of Lausanne (UNIL), Lausanne, Switzerland.
Maciej A KerlinCenter for Integrative Genomics (CIG), University of Lausanne (UNIL), Lausanne, Switzerland.
Ksenia KuznetsovaMax Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany.
Haruka OdaCell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
Hiroshi KimuraCell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.ORCID 0000-0003-0854-083X
Nadine L VastenhouwCenter for Integrative Genomics (CIG), University of Lausanne (UNIL), Lausanne, Switzerland. nadine.vastenhouw@unil.ch.ORCID 0000-0001-8782-9775
Max Planck Institute of Molecular Cell Biology and Genetics · DETokyo Institute of Technology · JPUniversity of Lausanne · CH

Funding

Boehringer Ingelheim Stiftung (Boehringer Ingelheim Foundation) naDeutsche Forschungsgemeinschaft (German Research Foundation) VA 1209/2-1EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101003023Max-Planck-Gesellschaft (Max Planck Society) naMEXT | Japan Society for the Promotion of Science (JSPS) JP18H05527MEXT | Japan Society for the Promotion of Science (JSPS) JP20K06484MEXT | Japan Society for the Promotion of Science (JSPS) JP21H04764Université de Lausanne (University of Lausanne) naVolkswagen Foundation (VolkswagenStiftung) 94773
6 · The paper itself

Abstract

The localization of transcriptional activity in specialized transcription bodies is a hallmark of gene expression in eukaryotic cells. It remains unclear, however, if and how transcription bodies affect gene expression. Here we disrupted the formation of two prominent endogenous transcription bodies that mark the onset of zygotic transcription in zebrafish embryos and analysed the effect on gene expression using enriched SLAM-seq and live-cell imaging. We find that the disruption of transcription bodies results in the misregulation of hundreds of genes. Here we focus on genes that are upregulated. These genes have accessible chromatin and are poised to be transcribed in the presence of the two transcription bodies, but they do not go into elongation. Live-cell imaging shows that disruption of the two large transcription bodies enables these poised genes to be transcribed in ectopic transcription bodies, suggesting that the large transcription bodies sequester a pause release factor. Supporting this hypothesis, we find that CDK9-the kinase that releases paused polymerase II-is highly enriched in the two large transcription bodies. Overexpression of CDK9 in wild-type embryos results in the formation of ectopic transcription bodies and thus phenocopies the removal of the two large transcription bodies. Taken together, our results show that transcription bodies regulate transcription by sequestering machinery, thereby preventing genes elsewhere in the nucleus from being transcribed.

Indexed as

Positive Transcriptional Elongation Factor BRNA Polymerase IIAnimalsChromatinCyclin-Dependent Kinase 9Gene ExpressionTranscription, GeneticZebrafishZebrafish ProteinsCdk9 protein, zebrafishChromatinCyclin-Dependent Kinase 9Positive Transcriptional Elongation Factor BRNA Polymerase IIZebrafish Proteins

Identifiers

PMID38589534
PMCPMC11021188
OpenAlexW4394577463

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.