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BEND3 safeguards pluripotency by repressing differentiation-associated genes
BEN domain–containing proteins are emerging rapidly as an important class of factors involved in modulating gene expression, yet the molecular basis of how they regulate chromatin function and transcription remains to be established. BEND3 is a quadruple BEN domain–containing protein that associates...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892337/ https://www.ncbi.nlm.nih.gov/pubmed/35217604 http://dx.doi.org/10.1073/pnas.2107406119 |
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author | Kurniawan, Fredy Chetlangia, Neha Kamran, Mohammad Redon, Christophe E. Pongor, Lorinc Sun, Qinyu Lin, Yo-Chuen Mohan, Vijay Shaqildi, Oways Asoudegi, Darya Hao, Qinyu Khan, Abid Aladjem, Mirit I. Prasanth, Kannanganattu V. Prasanth, Supriya G. |
author_facet | Kurniawan, Fredy Chetlangia, Neha Kamran, Mohammad Redon, Christophe E. Pongor, Lorinc Sun, Qinyu Lin, Yo-Chuen Mohan, Vijay Shaqildi, Oways Asoudegi, Darya Hao, Qinyu Khan, Abid Aladjem, Mirit I. Prasanth, Kannanganattu V. Prasanth, Supriya G. |
author_sort | Kurniawan, Fredy |
collection | PubMed |
description | BEN domain–containing proteins are emerging rapidly as an important class of factors involved in modulating gene expression, yet the molecular basis of how they regulate chromatin function and transcription remains to be established. BEND3 is a quadruple BEN domain–containing protein that associates with heterochromatin and functions as a transcriptional repressor. We find that BEND3 is highly expressed in pluripotent cells, and the induction of differentiation results in the down-regulation of BEND3. The removal of BEND3 from pluripotent cells results in cells exhibiting upregulation of the differentiation-inducing gene expression signature. We find that BEND3 binds to the promoters of differentiation-associated factors and key cell cycle regulators, including CDKN1A, encoding the cell cycle inhibitor p21, and represses the expression of differentiation-associated genes by enhancing H3K27me3 decoration at these promoters. Our results support a model in which transcription repression mediated by BEND3 is essential for normal development and to prevent differentiation. |
format | Online Article Text |
id | pubmed-8892337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-88923372022-08-25 BEND3 safeguards pluripotency by repressing differentiation-associated genes Kurniawan, Fredy Chetlangia, Neha Kamran, Mohammad Redon, Christophe E. Pongor, Lorinc Sun, Qinyu Lin, Yo-Chuen Mohan, Vijay Shaqildi, Oways Asoudegi, Darya Hao, Qinyu Khan, Abid Aladjem, Mirit I. Prasanth, Kannanganattu V. Prasanth, Supriya G. Proc Natl Acad Sci U S A Biological Sciences BEN domain–containing proteins are emerging rapidly as an important class of factors involved in modulating gene expression, yet the molecular basis of how they regulate chromatin function and transcription remains to be established. BEND3 is a quadruple BEN domain–containing protein that associates with heterochromatin and functions as a transcriptional repressor. We find that BEND3 is highly expressed in pluripotent cells, and the induction of differentiation results in the down-regulation of BEND3. The removal of BEND3 from pluripotent cells results in cells exhibiting upregulation of the differentiation-inducing gene expression signature. We find that BEND3 binds to the promoters of differentiation-associated factors and key cell cycle regulators, including CDKN1A, encoding the cell cycle inhibitor p21, and represses the expression of differentiation-associated genes by enhancing H3K27me3 decoration at these promoters. Our results support a model in which transcription repression mediated by BEND3 is essential for normal development and to prevent differentiation. National Academy of Sciences 2022-02-25 2022-03-01 /pmc/articles/PMC8892337/ /pubmed/35217604 http://dx.doi.org/10.1073/pnas.2107406119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Kurniawan, Fredy Chetlangia, Neha Kamran, Mohammad Redon, Christophe E. Pongor, Lorinc Sun, Qinyu Lin, Yo-Chuen Mohan, Vijay Shaqildi, Oways Asoudegi, Darya Hao, Qinyu Khan, Abid Aladjem, Mirit I. Prasanth, Kannanganattu V. Prasanth, Supriya G. BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title | BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title_full | BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title_fullStr | BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title_full_unstemmed | BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title_short | BEND3 safeguards pluripotency by repressing differentiation-associated genes |
title_sort | bend3 safeguards pluripotency by repressing differentiation-associated genes |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892337/ https://www.ncbi.nlm.nih.gov/pubmed/35217604 http://dx.doi.org/10.1073/pnas.2107406119 |
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