Evidence map›Paper›PMID 28056084›Full record

ArticlePLoS genetics2017

SBDS-Deficient Cells Have an Altered Homeostatic Equilibrium due to Translational Inefficiency Which Explains their Reduced Fitness and Provides a Logical Framework for Intervention.

Piera Calamita, Annarita Miluzio, Arianna Russo, Elisa Pesce, Sara Ricciardi, Farhat Khanim, Cristina Cheroni, Roberta Alfieri, Marilena Mancino, Chiara Gorrini and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.3field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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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

16 authors at 7 institutions in 3 countries.

Piera CalamitaINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.ORCID 0000-0002-3780-1050
Annarita MiluzioINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Arianna RussoINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Elisa PesceINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.ORCID 0000-0003-4214-1904
Sara RicciardiINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Farhat KhanimSchool of Biosciences, University of Birmingham Edgbaston Birmingham, United Kingdom.
Cristina CheroniINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Roberta AlfieriINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Marilena MancinoINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Chiara GorriniCampbell Family Institute for Breast Cancer Research, University Health Network, Toronto, Ontario, Canada.
Grazisa RossettiINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.ORCID 0000-0001-6361-311X
Ivana PelusoTelethon Institute of Genetics and Medicine (TIGEM)-Fondazione Telethon, Pozzuoli, Italy.
Massimiliano PaganiINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.
Diego L MedinaTelethon Institute of Genetics and Medicine (TIGEM)-Fondazione Telethon, Pozzuoli, Italy.
Johanna RommensSickKids Children Hospital, Toronto, Ontario, Canada.ORCID 0000-0001-8732-825X
Stefano BiffoINGM, National Institute of Molecular Genetics, "Romeo ed Enrica Invernizzi", Milan, Italy.ORCID 0000-0002-3780-1050
Istituto Nazionale Genetica Molecolare · ITTelethon Institute Of Genetics And Medicine · ITUniversity of Milan · ITSickKids Foundation · CAUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity Health Network · CAUniversity of Birmingham · GB

Funding

European Research Council 338999Telethon GGP10012
6 · The paper itself

Abstract

Ribosomopathies are a family of inherited disorders caused by mutations in genes necessary for ribosomal function. Shwachman-Diamond Bodian Syndrome (SDS) is an autosomal recessive disease caused, in most patients, by mutations of the SBDS gene. SBDS is a protein required for the maturation of 60S ribosomes. SDS patients present exocrine pancreatic insufficiency, neutropenia, chronic infections, and skeletal abnormalities. Later in life, patients are prone to myelodisplastic syndrome and acute myeloid leukemia (AML). It is unknown why patients develop AML and which cellular alterations are directly due to the loss of the SBDS protein. Here we derived mouse embryonic fibroblast lines from an SbdsR126T/R126T mouse model. After their immortalization, we reconstituted them by adding wild type Sbds. We then performed a comprehensive analysis of cellular functions including colony formation, translational and transcriptional RNA-seq, stress and drug sensitivity. We show that: 1. Mutant Sbds causes a reduction in cellular clonogenic capability and oncogene-induced transformation. 2. Mutant Sbds causes a marked increase in immature 60S subunits, limited impact on mRNA specific initiation of translation, but reduced global protein synthesis capability. 3. Chronic loss of SBDS activity leads to a rewiring of gene expression with reduced ribosomal capability, but increased lysosomal and catabolic activity. 4. Consistently with the gene signature, we found that SBDS loss causes a reduction in ATP and lactate levels, and increased susceptibility to DNA damage. Combining our data, we conclude that a cell-specific fragile phenotype occurs when SBDS protein drops below a threshold level, and propose a new interpretation of the disease.

Indexed as

HomeostasisPhenotypeAdenosine TriphosphateAnimalsCell LineCell Transformation, NeoplasticDNA DamageFibroblastsLactic AcidMiceProteinsRibosome Subunits, Large, EukaryoticRNA, MessengerAdenosine TriphosphateLactic AcidProteinsRNA, MessengerSbds protein, mouse

Identifiers

PMID28056084
PMCPMC5249248
OpenAlexW2569908555

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.