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ZBP-89 function in colonic stem cells and during butyrate-induced senescence
ZBP-89 (Zfp148, ZNF148) is a Kruppel-type zinc-finger family transcription factor that binds to GC-rich DNA elements. Earlier studies in cell lines demonstrated that ZBP-89 cooperates with Wnt β-catenin signaling by inducing β-catenin gene expression. Since β-catenin levels are normally highest at t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706877/ https://www.ncbi.nlm.nih.gov/pubmed/29212231 http://dx.doi.org/10.18632/oncotarget.21698 |
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author | Ocadiz-Ruiz, Ramon Photenhauer, Amanda L. Hayes, Michael M. Ding, Lin Fearon, Eric R. Merchant, Juanita L. |
author_facet | Ocadiz-Ruiz, Ramon Photenhauer, Amanda L. Hayes, Michael M. Ding, Lin Fearon, Eric R. Merchant, Juanita L. |
author_sort | Ocadiz-Ruiz, Ramon |
collection | PubMed |
description | ZBP-89 (Zfp148, ZNF148) is a Kruppel-type zinc-finger family transcription factor that binds to GC-rich DNA elements. Earlier studies in cell lines demonstrated that ZBP-89 cooperates with Wnt β-catenin signaling by inducing β-catenin gene expression. Since β-catenin levels are normally highest at the crypt base, we examined whether ZBP-89 is required for stem cell maintenance. Lineage-tracing using a Zfp148Cre(ERT2) transgenic line demonstrated expression in both intestine and colonic stem cells. Deleting the Zfp148 locus in the colon using the Cdx2NLSCre(ERT2) transgene, reduced the size and number of polyps formed in the Apc-deleted mice. Since colon polyps form in the presence of butyrate, a short chain fatty acid that suppresses cell growth, we examined the direct effect of butyrate on colon organoid survival. Butyrate induced senescence of colon organoids carrying the Apc deletion, only when Zfp148 was deleted. Using quantitative PCR and chromatin immunoprecipitation, we determined that butyrate treatment of colon cell lines suppressed ZNF148 gene expression, inducing CDKN2a (p16(Ink4a)) gene expression. Collectively, Zfp148 mRNA is expressed in CBCs, and is required for stem cell maintenance and colonic transformation. Butyrate induces colonic cell senescence in part through suppression of ZBP-89 gene expression and its subsequent occupancy of the CDKN2A promoter. |
format | Online Article Text |
id | pubmed-5706877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57068772017-12-05 ZBP-89 function in colonic stem cells and during butyrate-induced senescence Ocadiz-Ruiz, Ramon Photenhauer, Amanda L. Hayes, Michael M. Ding, Lin Fearon, Eric R. Merchant, Juanita L. Oncotarget Research Paper ZBP-89 (Zfp148, ZNF148) is a Kruppel-type zinc-finger family transcription factor that binds to GC-rich DNA elements. Earlier studies in cell lines demonstrated that ZBP-89 cooperates with Wnt β-catenin signaling by inducing β-catenin gene expression. Since β-catenin levels are normally highest at the crypt base, we examined whether ZBP-89 is required for stem cell maintenance. Lineage-tracing using a Zfp148Cre(ERT2) transgenic line demonstrated expression in both intestine and colonic stem cells. Deleting the Zfp148 locus in the colon using the Cdx2NLSCre(ERT2) transgene, reduced the size and number of polyps formed in the Apc-deleted mice. Since colon polyps form in the presence of butyrate, a short chain fatty acid that suppresses cell growth, we examined the direct effect of butyrate on colon organoid survival. Butyrate induced senescence of colon organoids carrying the Apc deletion, only when Zfp148 was deleted. Using quantitative PCR and chromatin immunoprecipitation, we determined that butyrate treatment of colon cell lines suppressed ZNF148 gene expression, inducing CDKN2a (p16(Ink4a)) gene expression. Collectively, Zfp148 mRNA is expressed in CBCs, and is required for stem cell maintenance and colonic transformation. Butyrate induces colonic cell senescence in part through suppression of ZBP-89 gene expression and its subsequent occupancy of the CDKN2A promoter. Impact Journals LLC 2017-10-09 /pmc/articles/PMC5706877/ /pubmed/29212231 http://dx.doi.org/10.18632/oncotarget.21698 Text en Copyright: © 2017 Ocadiz-Ruiz et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ocadiz-Ruiz, Ramon Photenhauer, Amanda L. Hayes, Michael M. Ding, Lin Fearon, Eric R. Merchant, Juanita L. ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title | ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title_full | ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title_fullStr | ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title_full_unstemmed | ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title_short | ZBP-89 function in colonic stem cells and during butyrate-induced senescence |
title_sort | zbp-89 function in colonic stem cells and during butyrate-induced senescence |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706877/ https://www.ncbi.nlm.nih.gov/pubmed/29212231 http://dx.doi.org/10.18632/oncotarget.21698 |
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