Transcriptional variability accelerates preleukemia by cell diversification and perturbation of protein synthesis.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
05 08 2022
Historique:
entrez: 3 8 2022
pubmed: 4 8 2022
medline: 6 8 2022
Statut: ppublish

Résumé

Transcriptional variability facilitates stochastic cell diversification and can in turn underpin adaptation to stress or injury. We hypothesize that it may analogously facilitate progression of premalignancy to cancer. To investigate this, we initiated preleukemia in mouse cells with enhanced transcriptional variability due to conditional disruption of the histone lysine acetyltransferase gene

Identifiants

pubmed: 35921412
doi: 10.1126/sciadv.abn4886
pmc: PMC9348803
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

eabn4886

Subventions

Organisme : Medical Research Council
ID : MC_PC_17230
Pays : United Kingdom

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Auteurs

Shikha Gupta (S)

Department of Genetics, University of Cambridge, Cambridge, UK.
Department of Haematology, University of Cambridge, Cambridge, UK.

Oliver M Dovey (OM)

Wellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK.

Ana Filipa Domingues (AF)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Oliwia W Cyran (OW)

Department of Haematology, University of Cambridge, Cambridge, UK.

Caitlin M Cash (CM)

College of Health, Medicine and Life Sciences - Division of Biosciences, Brunel University London, Uxbridge, UK.

George Giotopoulos (G)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Justyna Rak (J)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Jonathan Cooper (J)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Malgorzata Gozdecka (M)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Liza Dijkhuis (L)

College of Health, Medicine and Life Sciences - Division of Biosciences, Brunel University London, Uxbridge, UK.

Ryan J Asby (RJ)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Noor Al-Jabery (N)

College of Health, Medicine and Life Sciences - Division of Biosciences, Brunel University London, Uxbridge, UK.

Victor Hernandez-Hernandez (V)

College of Health, Medicine and Life Sciences - Division of Biosciences, Brunel University London, Uxbridge, UK.
Centre for Genome Engineering and Maintenance, Brunel University London, Uxbridge, UB8 3PH, UK.

Brian J Huntly (BJ)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

George S Vassiliou (GS)

Department of Haematology, University of Cambridge, Cambridge, UK.
Wellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK.
Wellcome Trust-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Cristina Pina (C)

College of Health, Medicine and Life Sciences - Division of Biosciences, Brunel University London, Uxbridge, UK.
Centre for Genome Engineering and Maintenance, Brunel University London, Uxbridge, UB8 3PH, UK.

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