Cargando…

KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF

Differentiated oligodendrocytes produce myelin and thereby ensure rapid nerve impulse conduction and efficient information processing in the vertebrate central nervous system. The Krüppel-like transcription factor KLF9 enhances oligodendrocyte differentiation in culture, but appears dispensable in v...

Descripción completa

Detalles Bibliográficos
Autores principales: Bernhardt, Celine, Sock, Elisabeth, Fröb, Franziska, Hillgärtner, Simone, Nemer, Mona, Wegner, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723594/
https://www.ncbi.nlm.nih.gov/pubmed/36318265
http://dx.doi.org/10.1093/nar/gkac953
_version_ 1784844217900597248
author Bernhardt, Celine
Sock, Elisabeth
Fröb, Franziska
Hillgärtner, Simone
Nemer, Mona
Wegner, Michael
author_facet Bernhardt, Celine
Sock, Elisabeth
Fröb, Franziska
Hillgärtner, Simone
Nemer, Mona
Wegner, Michael
author_sort Bernhardt, Celine
collection PubMed
description Differentiated oligodendrocytes produce myelin and thereby ensure rapid nerve impulse conduction and efficient information processing in the vertebrate central nervous system. The Krüppel-like transcription factor KLF9 enhances oligodendrocyte differentiation in culture, but appears dispensable in vivo. Its mode of action and role within the oligodendroglial gene regulatory network are unclear. Here we show that KLF9 shares its expression in differentiating oligodendrocytes with the closely related KLF13 protein. Both KLF9 and KLF13 bind to regulatory regions of genes that are important for oligodendrocyte differentiation and equally recognized by the central differentiation promoting transcription factors SOX10 and MYRF. KLF9 and KLF13 physically interact and synergistically activate oligodendrocyte-specific regulatory regions with SOX10 and MYRF. Similar to KLF9, KLF13 promotes differentiation and myelination in primary oligodendroglial cultures. Oligodendrocyte differentiation is also altered in KLF13-deficient mice as demonstrated by a transiently reduced myelin gene expression during the first postnatal week. Considering mouse phenotypes, the similarities in expression pattern and genomic binding and the behaviour in functional assays, KLF9 and KLF13 are important and largely redundant components of the gene regulatory network in charge of oligodendrocyte differentiation and myelination.
format Online
Article
Text
id pubmed-9723594
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-97235942022-12-07 KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF Bernhardt, Celine Sock, Elisabeth Fröb, Franziska Hillgärtner, Simone Nemer, Mona Wegner, Michael Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Differentiated oligodendrocytes produce myelin and thereby ensure rapid nerve impulse conduction and efficient information processing in the vertebrate central nervous system. The Krüppel-like transcription factor KLF9 enhances oligodendrocyte differentiation in culture, but appears dispensable in vivo. Its mode of action and role within the oligodendroglial gene regulatory network are unclear. Here we show that KLF9 shares its expression in differentiating oligodendrocytes with the closely related KLF13 protein. Both KLF9 and KLF13 bind to regulatory regions of genes that are important for oligodendrocyte differentiation and equally recognized by the central differentiation promoting transcription factors SOX10 and MYRF. KLF9 and KLF13 physically interact and synergistically activate oligodendrocyte-specific regulatory regions with SOX10 and MYRF. Similar to KLF9, KLF13 promotes differentiation and myelination in primary oligodendroglial cultures. Oligodendrocyte differentiation is also altered in KLF13-deficient mice as demonstrated by a transiently reduced myelin gene expression during the first postnatal week. Considering mouse phenotypes, the similarities in expression pattern and genomic binding and the behaviour in functional assays, KLF9 and KLF13 are important and largely redundant components of the gene regulatory network in charge of oligodendrocyte differentiation and myelination. Oxford University Press 2022-11-01 /pmc/articles/PMC9723594/ /pubmed/36318265 http://dx.doi.org/10.1093/nar/gkac953 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene regulation, Chromatin and Epigenetics
Bernhardt, Celine
Sock, Elisabeth
Fröb, Franziska
Hillgärtner, Simone
Nemer, Mona
Wegner, Michael
KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title_full KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title_fullStr KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title_full_unstemmed KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title_short KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF
title_sort klf9 and klf13 transcription factors boost myelin gene expression in oligodendrocytes as partners of sox10 and myrf
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723594/
https://www.ncbi.nlm.nih.gov/pubmed/36318265
http://dx.doi.org/10.1093/nar/gkac953
work_keys_str_mv AT bernhardtceline klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf
AT sockelisabeth klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf
AT frobfranziska klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf
AT hillgartnersimone klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf
AT nemermona klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf
AT wegnermichael klf9andklf13transcriptionfactorsboostmyelingeneexpressioninoligodendrocytesaspartnersofsox10andmyrf