The pluripotency transcription factor OCT4 represses heme oxygenase-1 gene expression.


Journal

FEBS letters
ISSN: 1873-3468
Titre abrégé: FEBS Lett
Pays: England
ID NLM: 0155157

Informations de publication

Date de publication:
07 2021
Historique:
revised: 17 05 2021
received: 14 04 2021
accepted: 23 05 2021
pubmed: 1 6 2021
medline: 5 8 2021
entrez: 31 5 2021
Statut: ppublish

Résumé

In embryonic stem (ES) cells, oxidative stress control is crucial for genomic stability, self-renewal, and cell differentiation. Heme oxygenase-1 (HO-1) is a key player of the antioxidant system and is also involved in stem cell differentiation and pluripotency acquisition. We found that the HO-1 gene is expressed in ES cells and induced after promoting differentiation. Moreover, downregulation of the pluripotency transcription factor (TF) OCT4 increased HO-1 mRNA levels in ES cells, and analysis of ChIP-seq public data revealed that this TF binds to the HO-1 gene locus in pluripotent cells. Finally, ectopic expression of OCT4 in heterologous systems repressed a reporter carrying the HO-1 gene promoter and the endogenous gene. Hence, this work highlights the connection between pluripotency and redox homeostasis.

Identifiants

pubmed: 34056710
doi: 10.1002/1873-3468.14138
doi:

Substances chimiques

Benzamides 0
Chir 99021 0
Membrane Proteins 0
Nanog Homeobox Protein 0
Nanog protein, mouse 0
Octamer Transcription Factor-3 0
Pou5f1 protein, mouse 0
Pyridines 0
Pyrimidines 0
RNA, Messenger 0
RNA, Small Interfering 0
SOXB1 Transcription Factors 0
Sox2 protein, mouse 0
Green Fluorescent Proteins 147336-22-9
mirdametinib 86K0J5AK6M
Diphenylamine 9N3CBB0BIQ
Luciferases EC 1.13.12.-
Heme Oxygenase-1 EC 1.14.14.18
Hmox1 protein, mouse EC 1.14.14.18

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1949-1961

Informations de copyright

© 2021 Federation of European Biochemical Societies.

Références

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Auteurs

María Victoria Petrone (MV)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Ayelén Toro (A)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Camila Vazquez Echegaray (C)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Marcos Gabriel Francia (MG)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Claudia Solari (C)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Maria Soledad Cosentino (MS)

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-UBA, Buenos Aires, Argentina.

Elba Vazquez (E)

Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales Universidad de Buenos Aires, Buenos Aires, Argentina.
IQUIBICEN, CONICET-UBA, Buenos Aires, Argentina.

Alejandra Guberman (A)

IQUIBICEN, CONICET-UBA, Buenos Aires, Argentina.
Departamento de Fisiología y Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales Universidad de Buenos Aires, Argentina.

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