Pioneer factors in development and cancer

Summary: Transcription factors (TFs) are essential mediators of epigenetic regulation and modifiers of penetrance. Studies from the past decades have revealed a sub-class of TF that is capable of remodeling closed chromatin states through targeting nucleosomal motifs. This pioneer factor (PF) class...

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Main Authors: Benjamin D. Sunkel, Benjamin Z. Stanton
Format: Article
Language:English
Published: Elsevier 2021-10-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004221011007
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spelling doaj-f640ff399fe646978277d300f58df3be2021-10-01T05:08:21ZengElsevieriScience2589-00422021-10-012410103132Pioneer factors in development and cancerBenjamin D. Sunkel0Benjamin Z. Stanton1Nationwide Children's Hospital, Center for Childhood Cancer and Blood Diseases, Columbus, OH 43205, USANationwide Children's Hospital, Center for Childhood Cancer and Blood Diseases, Columbus, OH 43205, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH 43205, USA; Department of Biological Chemistry and Pharmacology, The Ohio State University College of Medicine, Columbus, OH 43210, USA; Corresponding authorSummary: Transcription factors (TFs) are essential mediators of epigenetic regulation and modifiers of penetrance. Studies from the past decades have revealed a sub-class of TF that is capable of remodeling closed chromatin states through targeting nucleosomal motifs. This pioneer factor (PF) class of chromatin remodeler is ATP independent in its roles in epigenetic initiation, with nucleosome-motif recognition and association with repressive chromatin regions. Increasing evidence suggests that the fundamental properties of PFs can be coopted in human cancers. We explore the role of PFs in the larger context of tissue-specific epigenetic regulation. Moreover, we highlight an emerging class of chimeric PF derived from translocation partners in human disease and PFs associated with rare tumors. In the age of site-directed genome editing and targeted protein degradation, increasing our understanding of PFs will provide access to next-generation therapy for human disease driven from altered transcriptional circuitry.http://www.sciencedirect.com/science/article/pii/S2589004221011007Cancer systems biologyEpigeneticsMolecular biologySystems biology
collection DOAJ
language English
format Article
sources DOAJ
author Benjamin D. Sunkel
Benjamin Z. Stanton
spellingShingle Benjamin D. Sunkel
Benjamin Z. Stanton
Pioneer factors in development and cancer
iScience
Cancer systems biology
Epigenetics
Molecular biology
Systems biology
author_facet Benjamin D. Sunkel
Benjamin Z. Stanton
author_sort Benjamin D. Sunkel
title Pioneer factors in development and cancer
title_short Pioneer factors in development and cancer
title_full Pioneer factors in development and cancer
title_fullStr Pioneer factors in development and cancer
title_full_unstemmed Pioneer factors in development and cancer
title_sort pioneer factors in development and cancer
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2021-10-01
description Summary: Transcription factors (TFs) are essential mediators of epigenetic regulation and modifiers of penetrance. Studies from the past decades have revealed a sub-class of TF that is capable of remodeling closed chromatin states through targeting nucleosomal motifs. This pioneer factor (PF) class of chromatin remodeler is ATP independent in its roles in epigenetic initiation, with nucleosome-motif recognition and association with repressive chromatin regions. Increasing evidence suggests that the fundamental properties of PFs can be coopted in human cancers. We explore the role of PFs in the larger context of tissue-specific epigenetic regulation. Moreover, we highlight an emerging class of chimeric PF derived from translocation partners in human disease and PFs associated with rare tumors. In the age of site-directed genome editing and targeted protein degradation, increasing our understanding of PFs will provide access to next-generation therapy for human disease driven from altered transcriptional circuitry.
topic Cancer systems biology
Epigenetics
Molecular biology
Systems biology
url http://www.sciencedirect.com/science/article/pii/S2589004221011007
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