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Synthetic transcription factors switch from local to long-range control during cell differentiation
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4493938
Author(s) Wada, Takeo; Wallerich, Sandrine; Becskei, Attila
Author(s) at UniBasel Becskei, Attila
Wada, Takeo
Wallerich, Sandrine
Year 2019
Title Synthetic transcription factors switch from local to long-range control during cell differentiation
Journal ACS Synthetic Biology
Volume 8
Number 2
Pages / Article-Number 223-231
Mesh terms Animals; Cell Differentiation, physiology; Cells, Cultured; Embryonic Stem Cells, metabolism; Epigenesis, Genetic, genetics; Gene Expression Regulation, physiology; Mice; Promoter Regions, Genetic, genetics; Synthetic Biology; Transcription Factors, metabolism; Transcription, Genetic, genetics
Abstract Genes, including promoters and enhancers, are regulated by short- and long-range interactions in higher eukaryotes. It is unclear how mammalian gene expression subject to such a combinatorial regulation can be controlled by synthetic transcription factors (TF). Here, we studied how synthetic TALE transcriptional activators and repressors affect the expression of genes in a gene array during cellular differentiation. The protocadherin gene array is silent in mouse embryonic stem (ES) and neuronal progenitor cells. The TALE transcriptional activator recruited to a promoter activates specifically the target gene in ES cells. Upon differentiation into neuronal progenitors, the transcriptional regulatory logic changes: the same activator behaves like an enhancer, activating distant genes in a correlated, stochastic fashion. The long-range effect is reflected by the alterations in CpG methylation. Our findings reveal the limits of precision and the opportunities in the control of gene expression for TF-based therapies in cells of various differentiation stages.
Publisher American Chemical Society
ISSN/ISBN 2161-5063
edoc-URL https://edoc.unibas.ch/68201/
Full Text on edoc No
Digital Object Identifier DOI 10.1021/acssynbio.8b00369
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/30624895
Document type (ISI) Journal Article
 
   

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