Evidence map›Paper›PMID 29422612›Full record

ArticleScientific reports2018

Csde1 binds transcripts involved in protein homeostasis and controls their expression in an erythroid cell line.

Kat S Moore, Nurcan Yagci, Floris van Alphen, Nahuel A Paolini, Rastislav Horos, Ntsiki M Held, Riekelt H Houtkooper, Emile van den Akker, Alexander B Meijer, Peter A C 't Hoen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Review
  6. CSDE1 promotes miR-451 biogenesis.Nucleic acids research · 2023
    Article
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  14. The role of CSDE1 in translational reprogramming and human diseases.Cell communication and signaling : CCS · 2020
    Review
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  18. Review
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 at 5 institutions in 2 countries.

Kat S MooreDepartment Hematopoiesis, Sanquin, and Landsteiner Laboratory AMC/UvA, 1066 CX, Amsterdam, The Netherlands.
Nurcan YagciDepartment Hematopoiesis, Sanquin, and Landsteiner Laboratory AMC/UvA, 1066 CX, Amsterdam, The Netherlands.
Floris van AlphenDepartment of Plasma proteins, Sanquin Research, 1066 CX, Amsterdam, The Netherlands.
Nahuel A PaoliniDepartment Hematopoiesis, Sanquin, and Landsteiner Laboratory AMC/UvA, 1066 CX, Amsterdam, The Netherlands.
Rastislav HorosEuropean Molecular Biology Laboratory, 69117, Heidelberg, Germany.
Ntsiki M HeldLaboratory Genetic Metabolic Diseases, Academic Medical Center, 1105 AZ, Amsterdam, The Netherlands.
Riekelt H HoutkooperLaboratory Genetic Metabolic Diseases, Academic Medical Center, 1105 AZ, Amsterdam, The Netherlands.
Emile van den AkkerDepartment Hematopoiesis, Sanquin, and Landsteiner Laboratory AMC/UvA, 1066 CX, Amsterdam, The Netherlands.
Alexander B MeijerDepartment of Plasma proteins, Sanquin Research, 1066 CX, Amsterdam, The Netherlands.
Peter A C 't HoenCenter for Human and Clinical Genetics, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.ORCID 0000-0003-4450-3112
Marieke von LindernDepartment Hematopoiesis, Sanquin, and Landsteiner Laboratory AMC/UvA, 1066 CX, Amsterdam, The Netherlands. m.vonlindern@sanquin.nl.
Sanquin · NLAmsterdam UMC Location University of Amsterdam · NLEuropean Molecular Biology Laboratory · DELeiden University Medical Center · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression of the RNA-binding protein Csde1 (Cold shock domain protein e1) is strongly upregulated during erythropoiesis compared to other hematopoietic lineages. Csde1 expression is impaired in the severe congenital anemia Diamond Blackfan Anemia (DBA), and reduced expression of Csde1 in healthy erythroblasts impaired their proliferation and differentiation. To investigate the cellular pathways controlled by Csde1 in erythropoiesis, we identified the transcripts that physically associate with Csde1 in erythroid cells. These mainly encoded proteins involved in ribogenesis, mRNA translation and protein degradation, but also proteins associated with the mitochondrial respiratory chain and mitosis. Crispr/Cas9-mediated deletion of the first cold shock domain of Csde1 affected RNA expression and/or protein expression of Csde1-bound transcripts. For instance, protein expression of Pabpc1 was enhanced while Pabpc1 mRNA expression was reduced indicating more efficient translation of Pabpc1 followed by negative feedback on mRNA stability. Overall, the effect of reduced Csde1 function on mRNA stability and translation of Csde1-bound transcripts was modest. Clones with complete loss of Csde1, however, could not be generated. We suggest that Csde1 is involved in feed-back control in protein homeostasis and that it dampens stochastic changes in mRNA expression.

Indexed as

Gene Expression RegulationProteostasisAnimalsCRISPR-Cas SystemsDNA-Binding ProteinsErythroid CellsErythropoiesisHEK293 CellsHumansPoly(A)-Binding ProteinsRNA-Binding ProteinsRNA, MessengerTumor Cells, CulturedCSDE1 protein, humanDNA-Binding ProteinsPABPC1L protein, humanPoly(A)-Binding ProteinsRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID29422612
PMCPMC5805679
OpenAlexW2799813282

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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.