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CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models
The CREB3 subfamily of membrane-bound bZIP transcription factors has five members in mammals known as CREB3 and CREB3L1-L4. One current model suggests that CREB3 subfamily transcription factors are similar to ATF6 in regulated intramembrane proteolysis and transcriptional activation. Particularly, t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116243/ https://www.ncbi.nlm.nih.gov/pubmed/21711675 http://dx.doi.org/10.1186/2045-3701-1-6 |
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author | Chan, Chi-Ping Kok, Kin-Hang Jin, Dong-Yan |
author_facet | Chan, Chi-Ping Kok, Kin-Hang Jin, Dong-Yan |
author_sort | Chan, Chi-Ping |
collection | PubMed |
description | The CREB3 subfamily of membrane-bound bZIP transcription factors has five members in mammals known as CREB3 and CREB3L1-L4. One current model suggests that CREB3 subfamily transcription factors are similar to ATF6 in regulated intramembrane proteolysis and transcriptional activation. Particularly, they were all thought to be proteolytically activated in response to endoplasmic reticulum (ER) stress to stimulate genes that are involved in unfolded protein response (UPR). Although the physiological inducers of their proteolytic activation remain to be identified, recent findings from microarray analyses, RNAi screens and gene knockouts not only demonstrated their critical roles in regulating development, metabolism, secretion, survival and tumorigenesis, but also revealed cell type-specific patterns in the activation of their target genes. Members of the CREB3 subfamily show differential activity despite their structural similarity. The spectrum of their biological function expands beyond ER stress and UPR. Further analyses are required to elucidate the mechanism of their proteolytic activation and the molecular basis of their target recognition. |
format | Online Article Text |
id | pubmed-3116243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31162432011-06-16 CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models Chan, Chi-Ping Kok, Kin-Hang Jin, Dong-Yan Cell Biosci Review The CREB3 subfamily of membrane-bound bZIP transcription factors has five members in mammals known as CREB3 and CREB3L1-L4. One current model suggests that CREB3 subfamily transcription factors are similar to ATF6 in regulated intramembrane proteolysis and transcriptional activation. Particularly, they were all thought to be proteolytically activated in response to endoplasmic reticulum (ER) stress to stimulate genes that are involved in unfolded protein response (UPR). Although the physiological inducers of their proteolytic activation remain to be identified, recent findings from microarray analyses, RNAi screens and gene knockouts not only demonstrated their critical roles in regulating development, metabolism, secretion, survival and tumorigenesis, but also revealed cell type-specific patterns in the activation of their target genes. Members of the CREB3 subfamily show differential activity despite their structural similarity. The spectrum of their biological function expands beyond ER stress and UPR. Further analyses are required to elucidate the mechanism of their proteolytic activation and the molecular basis of their target recognition. BioMed Central 2011-02-17 /pmc/articles/PMC3116243/ /pubmed/21711675 http://dx.doi.org/10.1186/2045-3701-1-6 Text en Copyright ©2011 Chan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Chan, Chi-Ping Kok, Kin-Hang Jin, Dong-Yan CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title | CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title_full | CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title_fullStr | CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title_full_unstemmed | CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title_short | CREB3 subfamily transcription factors are not created equal: Recent insights from global analyses and animal models |
title_sort | creb3 subfamily transcription factors are not created equal: recent insights from global analyses and animal models |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116243/ https://www.ncbi.nlm.nih.gov/pubmed/21711675 http://dx.doi.org/10.1186/2045-3701-1-6 |
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