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Transcription of the Geminin gene is regulated by a negative-feedback loop

Geminin performs a central function in regulating cellular proliferation and differentiation in development and also in stem cells. Of interest, down-regulation of Geminin induces gene transcription regulated by E2F, indicating that Geminin is involved in regulation of E2F-mediated transcriptional a...

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Autores principales: Ohno, Yoshinori, Saeki, Keita, Yasunaga, Shin'ichiro, Kurogi, Toshiaki, Suzuki-Takedachi, Kyoko, Shirai, Manabu, Mihara, Keichiro, Yoshida, Kenichi, Voncken, J. Willem, Ohtsubo, Motoaki, Takihara, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983001/
https://www.ncbi.nlm.nih.gov/pubmed/24554762
http://dx.doi.org/10.1091/mbc.E13-09-0534
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author Ohno, Yoshinori
Saeki, Keita
Yasunaga, Shin'ichiro
Kurogi, Toshiaki
Suzuki-Takedachi, Kyoko
Shirai, Manabu
Mihara, Keichiro
Yoshida, Kenichi
Voncken, J. Willem
Ohtsubo, Motoaki
Takihara, Yoshihiro
author_facet Ohno, Yoshinori
Saeki, Keita
Yasunaga, Shin'ichiro
Kurogi, Toshiaki
Suzuki-Takedachi, Kyoko
Shirai, Manabu
Mihara, Keichiro
Yoshida, Kenichi
Voncken, J. Willem
Ohtsubo, Motoaki
Takihara, Yoshihiro
author_sort Ohno, Yoshinori
collection PubMed
description Geminin performs a central function in regulating cellular proliferation and differentiation in development and also in stem cells. Of interest, down-regulation of Geminin induces gene transcription regulated by E2F, indicating that Geminin is involved in regulation of E2F-mediated transcriptional activity. Because transcription of the Geminin gene is reportedly regulated via an E2F-responsive region (E2F-R) located in the first intron, we first used a reporter vector to examine the effect of Geminin on E2F-mediated transcriptional regulation. We found that Geminin transfection suppressed E2F1- and E2F2-mediated transcriptional activation and also mildly suppressed such activity in synergy with E2F5, 6, and 7, suggesting that Geminin constitutes a negative-feedback loop for the Geminin promoter. Of interest, Geminin also suppressed nuclease accessibility, acetylation of histone H3, and trimethylation of histone H3 at lysine 4, which were induced by E2F1 overexpression, and enhanced tri­methylation of histone H3 at lysine 27 and monoubiquitination of histone H2A at lysine 119 in E2F-R. However, Geminin5EQ, which does not interact with Brahma or Brg1, did not suppress accessibility to nuclease digestion or transcription but had an overall dominant-negative effect. These findings suggest that E2F-mediated activation of Geminin transcription is negatively regulated by Geminin through the inhibition of chromatin remodeling.
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spelling pubmed-39830012014-06-30 Transcription of the Geminin gene is regulated by a negative-feedback loop Ohno, Yoshinori Saeki, Keita Yasunaga, Shin'ichiro Kurogi, Toshiaki Suzuki-Takedachi, Kyoko Shirai, Manabu Mihara, Keichiro Yoshida, Kenichi Voncken, J. Willem Ohtsubo, Motoaki Takihara, Yoshihiro Mol Biol Cell Articles Geminin performs a central function in regulating cellular proliferation and differentiation in development and also in stem cells. Of interest, down-regulation of Geminin induces gene transcription regulated by E2F, indicating that Geminin is involved in regulation of E2F-mediated transcriptional activity. Because transcription of the Geminin gene is reportedly regulated via an E2F-responsive region (E2F-R) located in the first intron, we first used a reporter vector to examine the effect of Geminin on E2F-mediated transcriptional regulation. We found that Geminin transfection suppressed E2F1- and E2F2-mediated transcriptional activation and also mildly suppressed such activity in synergy with E2F5, 6, and 7, suggesting that Geminin constitutes a negative-feedback loop for the Geminin promoter. Of interest, Geminin also suppressed nuclease accessibility, acetylation of histone H3, and trimethylation of histone H3 at lysine 4, which were induced by E2F1 overexpression, and enhanced tri­methylation of histone H3 at lysine 27 and monoubiquitination of histone H2A at lysine 119 in E2F-R. However, Geminin5EQ, which does not interact with Brahma or Brg1, did not suppress accessibility to nuclease digestion or transcription but had an overall dominant-negative effect. These findings suggest that E2F-mediated activation of Geminin transcription is negatively regulated by Geminin through the inhibition of chromatin remodeling. The American Society for Cell Biology 2014-04-15 /pmc/articles/PMC3983001/ /pubmed/24554762 http://dx.doi.org/10.1091/mbc.E13-09-0534 Text en © 2014 Ohno et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Ohno, Yoshinori
Saeki, Keita
Yasunaga, Shin'ichiro
Kurogi, Toshiaki
Suzuki-Takedachi, Kyoko
Shirai, Manabu
Mihara, Keichiro
Yoshida, Kenichi
Voncken, J. Willem
Ohtsubo, Motoaki
Takihara, Yoshihiro
Transcription of the Geminin gene is regulated by a negative-feedback loop
title Transcription of the Geminin gene is regulated by a negative-feedback loop
title_full Transcription of the Geminin gene is regulated by a negative-feedback loop
title_fullStr Transcription of the Geminin gene is regulated by a negative-feedback loop
title_full_unstemmed Transcription of the Geminin gene is regulated by a negative-feedback loop
title_short Transcription of the Geminin gene is regulated by a negative-feedback loop
title_sort transcription of the geminin gene is regulated by a negative-feedback loop
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983001/
https://www.ncbi.nlm.nih.gov/pubmed/24554762
http://dx.doi.org/10.1091/mbc.E13-09-0534
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