Evidence map›Paper›PMID 24959908›Full record

ArticlePloS one2014

RPLP1, a crucial ribosomal protein for embryonic development of the nervous system.

Laura Perucho, Ana Artero-Castro, Sergi Guerrero, Santiago Ramón y Cajal, Matilde E LLeonart, Zhao-Qi Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

34 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  4. The multifaceted roles of ribosomal P complex in cancer.World journal of surgical oncology · 2025
    Review
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  11. Loss of function of ribosomal protein L13a blocks blastocyst formation and reveals a potential nuclear role in gene expression.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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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 2 institutions in 2 countries.

Laura PeruchoLeibniz Institute for Age Research - Fritz Lipmann Institute (FLI), Jena, Germany.
Ana Artero-CastroOncology and Pathology Group, Institut de Recerca Hospital Vall d'Hebron, Barcelona, Spain.
Sergi GuerreroOncology and Pathology Group, Institut de Recerca Hospital Vall d'Hebron, Barcelona, Spain.
Santiago Ramón y CajalOncology and Pathology Group, Institut de Recerca Hospital Vall d'Hebron, Barcelona, Spain.
Matilde E LLeonartOncology and Pathology Group, Institut de Recerca Hospital Vall d'Hebron, Barcelona, Spain.
Zhao-Qi WangLeibniz Institute for Age Research - Fritz Lipmann Institute (FLI), Jena, Germany; Faculty of Biology and Pharmacy, Friedrich Schiller University of Jena, Jena, Germany.
Vall d'Hebron Institut de Recerca · ESLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosomal proteins are pivotal to development and tissue homeostasis. RP Large P1 (Rplp1) overexpression is associated with tumorigenesis. However, the physiological function of Rplp1 in mammalian development remains unknown. In this study, we disrupted Rplp1 in the mouse germline and central nervous system (Rplp1CNSΔ). Rplp1 heterozygosity caused body size reductions, male infertility, systemic abnormalities in various tissues and a high frequency of early postnatal death. Rplp1CNSΔ newborn mice exhibited perinatal lethality and brain atrophy with size reductions of the neocortex, midbrain and ganglionic eminence. The Rplp1 knockout neocortex exhibited progenitor cell proliferation arrest and apoptosis due to the dysregulation of key cell cycle and apoptosis regulators (cyclin A, cyclin E, p21CIP1, p27KIP1, p53). Similarly, Rplp1 deletion in pMEFs led to proliferation arrest and premature senescence. Importantly, Rplp1 deletion in primary mouse embryonic fibroblasts did not alter global protein synthesis, but did change the expression patterns of specific protein subsets involved in protein folding and the unfolded protein response, cell death, protein transport and signal transduction, among others. Altogether, we demonstrated that the translation "fine-tuning" exerted by Rplp1 is essential for embryonic and brain development and for proper cell proliferation.

Indexed as

Gene DeletionAnimalsAnimals, NewbornBody SizeCell ProliferationCells, CulturedCongenital AbnormalitiesFibroblastsGene Knockout TechniquesGenes, EssentialGenes, LethalInfertility, MaleMaleMiceNervous SystemRibosomal ProteinsRibosomal ProteinsRPLP1 protein, mouse

Identifiers

PMID24959908
PMCPMC4069005
OpenAlexW2042957860

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.