Evidence map›Paper›PMID 24038356›Full record

ArticleNucleic acids research2013

The splicing landscape is globally reprogrammed during male meiosis.

Ralf Schmid, Sushma Nagaraja Grellscheid, Ingrid Ehrmann, Caroline Dalgliesh, Marina Danilenko, Maria Paola Paronetto, Simona Pedrotti, David Grellscheid, Richard J Dixon, Claudio Sette and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

58 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
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  3. Ultra-Conserved Poison Exons Enable Rapid and Safe Splicing Factor Gene Expression Switches: A Hypothesis.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
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  11. Review
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  16. Article
  17. iScience · 2023
    Article
  18. SRSF1-mediated alternative splicing is required for spermatogenesis.International journal of biological sciences · 2023
    Article
  19. Article
  20. Article
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

12 authors at 4 institutions in 2 countries.

Ralf SchmidDepartment of Biochemistry, University of Leicester, Leicester, LE1 9HN, UK, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK, School of Biological and Biomedical Sciences, Durham University, Durham, DH1 3LE, UK, Department of Health Sciences, University of 00135 Rome 'Foro Italico', Rome, Italy, Laboratories of Neuroembryology and of Cellular and Molecular Neurobiology, Fondazione Santa Lucia IRCCS, 00143 Rome, Italy, Department of Public Health and Cell Biology, University of Rome Tor Vergata, 00133 Rome, Italy, Institute of Particle Physics Phenomenology, Durham University, Durham, DH1 3LE, UK and Life Technologies Ltd., Paisley PA4 9RF, UK.
Sushma Nagaraja Grellscheid
Ingrid Ehrmann
Caroline Dalgliesh
Marina Danilenko
Maria Paola Paronetto
Simona Pedrotti
David Grellscheid
Richard J Dixon
Claudio Sette
Ian C Eperon
David J Elliott
Durham University · GBFondazione Santa Lucia · ITNewcastle University · GBUniversity of Leicester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D013917/1Biotechnology and Biological Sciences Research Council BB/I006923/1Telethon GGP09154Wellcome Trust WT080368MAWellcome Trust WT089225/Z/09/Z
6 · The paper itself

Abstract

Meiosis requires conserved transcriptional changes, but it is not known whether there is a corresponding set of RNA splicing switches. Here, we used RNAseq of mouse testis to identify changes associated with the progression from mitotic spermatogonia to meiotic spermatocytes. We identified ∼150 splicing switches, most of which affect conserved protein-coding exons. The expression of many key splicing regulators changed in the course of meiosis, including downregulation of polypyrimidine tract binding protein (PTBP1) and heterogeneous nuclear RNP A1, and upregulation of nPTB, Tra2β, muscleblind, CELF proteins, Sam68 and T-STAR. The sequences near the regulated exons were significantly enriched in target sites for PTB, Tra2β and STAR proteins. Reporter minigene experiments investigating representative exons in transfected cells showed that PTB binding sites were critical for splicing of a cassette exon in the Ralgps2 mRNA and a shift in alternative 5' splice site usage in the Bptf mRNA. We speculate that nPTB might functionally replace PTBP1 during meiosis for some target exons, with changes in the expression of other splicing factors helping to establish meiotic splicing patterns. Our data suggest that there are substantial changes in the determinants and patterns of alternative splicing in the mitotic-to-meiotic transition of the germ cell cycle.

Indexed as

Alternative SplicingAnimalsBase SequenceExonsMaleMeiosisMiceMolecular Sequence DataRNA-Binding ProteinsRNA IsoformsSequence Analysis, RNASpermatocytesSpermatogoniaTestisTranscriptomeRNA-Binding ProteinsRNA Isoforms

Identifiers

PMID24038356
PMCPMC3905889
OpenAlexW2114383979

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.