NONO Is a Negative Regulator of


Journal

Cancer genomics & proteomics
ISSN: 1790-6245
Titre abrégé: Cancer Genomics Proteomics
Pays: Greece
ID NLM: 101188791

Informations de publication

Date de publication:
Historique:
received: 25 03 2020
revised: 28 04 2020
accepted: 29 04 2020
entrez: 25 6 2020
pubmed: 25 6 2020
medline: 12 2 2021
Statut: ppublish

Résumé

Sex determining region Y (SRY)-box 2 (SOX2) is a transcription factor essential for the maintenance of proliferation and self-renewal of cancer stem cells and is associated with breast cancer initiation. Regulation of cancer stem cell plasticity by SOX2 requires both positive and negative SOX2 transcription factors, but the negative regulator is still largely unknown. SOX2 promoter-binding proteins were identified by liquid chromatography-mass spectrometry/mass spectrometry, luciferase assay, and chromatin immunoprecipitation. The effects of one such transcription factor on SOX2 expression was investigated by knockdown and overexpression experiments. Non-POU domain-containing octamer-binding protein (NONO) (also known as 54-kDa nuclear RNA-binding protein, P54NRB) was identified as a SOX2 promoter-binding protein and a negative regulator of SOX2 expression. Its activity was controlled by its coiled-coil domain and the C-terminal domain. These results suggest that NONO acts as a key regulator of SOX2 transcription through the repression of SOX2 promoter activity in breast cancer cells.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Sex determining region Y (SRY)-box 2 (SOX2) is a transcription factor essential for the maintenance of proliferation and self-renewal of cancer stem cells and is associated with breast cancer initiation. Regulation of cancer stem cell plasticity by SOX2 requires both positive and negative SOX2 transcription factors, but the negative regulator is still largely unknown.
MATERIALS AND METHODS METHODS
SOX2 promoter-binding proteins were identified by liquid chromatography-mass spectrometry/mass spectrometry, luciferase assay, and chromatin immunoprecipitation. The effects of one such transcription factor on SOX2 expression was investigated by knockdown and overexpression experiments.
RESULTS RESULTS
Non-POU domain-containing octamer-binding protein (NONO) (also known as 54-kDa nuclear RNA-binding protein, P54NRB) was identified as a SOX2 promoter-binding protein and a negative regulator of SOX2 expression. Its activity was controlled by its coiled-coil domain and the C-terminal domain.
CONCLUSION CONCLUSIONS
These results suggest that NONO acts as a key regulator of SOX2 transcription through the repression of SOX2 promoter activity in breast cancer cells.

Identifiants

pubmed: 32576581
pii: 17/4/359
doi: 10.21873/cgp.20195
pmc: PMC7367599
doi:

Substances chimiques

Biomarkers, Tumor 0
DNA-Binding Proteins 0
NONO protein, human 0
RNA-Binding Proteins 0
SOX2 protein, human 0
SOXB1 Transcription Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

359-367

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

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Auteurs

Shanshan Liang (S)

The Key Laboratory of Biomarker High-throughput Screening and Target Translation of Breast and Gastrointestinal Tumor, Oncology Department, Affiliated Zhongshan Hospital of Dalian University, Dalian, P.R. China.
Department of Microbiology, Faculty of Medicine, Shimane University, Shimane, Japan.
Division of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University, Hokkaido, Japan.

Hidehisa Takahashi (H)

Department of Biochemistry, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Department of Molecular Biology, Yokohama City University School of Medicine, Yokohama City University Graduate School of Medical Science, Yokohama, Japan.

Tetsuro Hirose (T)

Division of RNA Bio-function, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.

Yasuhiro Kuramitsu (Y)

Health Science University of Hokkaido School of Nursing & Social Services, Hokkaido, Japan.

Shigetsugu Hatakeyama (S)

Department of Biochemistry, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

Hironori Yoshiyama (H)

Department of Microbiology, Faculty of Medicine, Shimane University, Shimane, Japan.

Ruoyu Wang (R)

The Key Laboratory of Biomarker High-throughput Screening and Target Translation of Breast and Gastrointestinal Tumor, Oncology Department, Affiliated Zhongshan Hospital of Dalian University, Dalian, P.R. China.

Jun-Ichi Hamada (JI)

Division of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University, Hokkaido, Japan jun1hamada@hoku-iryo-u.ac.jp iizasah@med.shimane-u.ac.jp.
Health Science University of Hokkaido School of Nursing & Social Services, Hokkaido, Japan.

Hisashi Iizasa (H)

Department of Microbiology, Faculty of Medicine, Shimane University, Shimane, Japan jun1hamada@hoku-iryo-u.ac.jp iizasah@med.shimane-u.ac.jp.
Division of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University, Hokkaido, Japan.

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Classifications MeSH