Transcription Factors Modulate c-Fos Transcriptional Bursts
Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)—especially in rapidly inducible systems—is largely unknown. Using fluorescence...
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Published in: | Cell reports (Cambridge) Vol. 8; no. 1; pp. 75 - 83 |
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Abstract | Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)—especially in rapidly inducible systems—is largely unknown. Using fluorescence in situ hybridization and computational models, we quantified the transcriptional activity of the proto-oncogene c-Fos with single mRNA accuracy at individual endogenous alleles. We showed that, during MAPK induction, the TF concentration modulates the burst frequency of c-Fos, whereas other bursting parameters remain mostly unchanged. By using synthetic TFs with TALE DNA-binding domains, we systematically altered different aspects of these bursts. Specifically, we linked the polymerase initiation frequency to the strength of the transactivation domain and the burst duration to the TF lifetime on the promoter. Our results show how TFs and promoter binding domains collectively act to regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes.
[Display omitted]
•Single mRNA quantification and modeling reveal complex c-Fos regulation dynamics•Transcription factor concentrations control c-Fos burst activation frequencies•Transcription factor-DNA interaction controls burst duration•Strength of transactivation domains control initiation frequency
Transcription is a stochastic process mostly occurring in episodic bursts. The impact of transcription factors (TFs) on bursting behavior is largely unknown. Using FISH and computational modeling, Senecal et al. now link (1) TF concentration with transcription bursting frequency, (2) TF-DNA association with burst duration, and (3) TF transactivation domain strength with polymerase initiation frequency. This work shows how TFs regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. |
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AbstractList | Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)—especially in rapidly inducible systems—is largely unknown. Using fluorescence in situ hybridization and computational models, we quantified the transcriptional activity of the proto-oncogene c-Fos with single mRNA accuracy at individual endogenous alleles. We showed that, during MAPK induction, the TF concentration modulates the burst frequency of c-Fos, whereas other bursting parameters remain mostly unchanged. By using synthetic TFs with TALE DNA-binding domains, we systematically altered different aspects of these bursts. Specifically, we linked the polymerase initiation frequency to the strength of the transactivation domain and the burst duration to the TF lifetime on the promoter. Our results show how TFs and promoter binding domains collectively act to regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chro-matin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)—especially in rapidly inducible systems—is largely unknown. Using fluorescence in situ hybridization and computational models, we quantified the transcriptional activity of the proto-oncogene c-Fos with single mRNA accuracy at individual endogenous alleles. We showed that, during MAPK induction, the TF concentration modulates the burst frequency of c-Fos, whereas other bursting parameters remain mostly unchanged. By using synthetic TFs with TALE DNA-binding domains, we systematically altered different aspects of these bursts. Specifically, we linked the polymerase initiation frequency to the strength of the transactivation domain and the burst duration to the TF lifetime on the promoter. Our results show how TFs and promoter binding domains collectively act to regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)—especially in rapidly inducible systems—is largely unknown. Using fluorescence in situ hybridization and computational models, we quantified the transcriptional activity of the proto-oncogene c-Fos with single mRNA accuracy at individual endogenous alleles. We showed that, during MAPK induction, the TF concentration modulates the burst frequency of c-Fos, whereas other bursting parameters remain mostly unchanged. By using synthetic TFs with TALE DNA-binding domains, we systematically altered different aspects of these bursts. Specifically, we linked the polymerase initiation frequency to the strength of the transactivation domain and the burst duration to the TF lifetime on the promoter. Our results show how TFs and promoter binding domains collectively act to regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. [Display omitted] •Single mRNA quantification and modeling reveal complex c-Fos regulation dynamics•Transcription factor concentrations control c-Fos burst activation frequencies•Transcription factor-DNA interaction controls burst duration•Strength of transactivation domains control initiation frequency Transcription is a stochastic process mostly occurring in episodic bursts. The impact of transcription factors (TFs) on bursting behavior is largely unknown. Using FISH and computational modeling, Senecal et al. now link (1) TF concentration with transcription bursting frequency, (2) TF-DNA association with burst duration, and (3) TF transactivation domain strength with polymerase initiation frequency. This work shows how TFs regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior on long timescales, the impact of transcription factors (TFs)--especially in rapidly inducible systems--is largely unknown. Using fluorescence in situ hybridization and computational models, we quantified the transcriptional activity of the proto-oncogene c-Fos with single mRNA accuracy at individual endogenous alleles. We showed that, during MAPK induction, the TF concentration modulates the burst frequency of c-Fos, whereas other bursting parameters remain mostly unchanged. By using synthetic TFs with TALE DNA-binding domains, we systematically altered different aspects of these bursts. Specifically, we linked the polymerase initiation frequency to the strength of the transactivation domain and the burst duration to the TF lifetime on the promoter. Our results show how TFs and promoter binding domains collectively act to regulate different bursting parameters, offering a vast, evolutionarily tunable regulatory range for individual genes. |
Author | Proux, Florence Mueller, Florian Zimmer, Christophe Senecal, Adrien Ly, Nathalie Darzacq, Xavier Munsky, Brian Braye, Floriane E. |
AuthorAffiliation | 5 Institut Pasteur, Unité Imagerie et Modélisation, CNRS Unité de Recherche Associée 2582, 75015 Paris, France 2 Transcription Imaging Consortium, Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA 3 UPMC University Paris 06, 75005 Paris, France 1 Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France 4 Department of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO 80523, USA |
AuthorAffiliation_xml | – name: 3 UPMC University Paris 06, 75005 Paris, France – name: 1 Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – name: 5 Institut Pasteur, Unité Imagerie et Modélisation, CNRS Unité de Recherche Associée 2582, 75015 Paris, France – name: 2 Transcription Imaging Consortium, Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA – name: 4 Department of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO 80523, USA |
Author_xml | – sequence: 1 givenname: Adrien surname: Senecal fullname: Senecal, Adrien organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – sequence: 2 givenname: Brian surname: Munsky fullname: Munsky, Brian organization: Department of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO 80523, USA – sequence: 3 givenname: Florence surname: Proux fullname: Proux, Florence organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – sequence: 4 givenname: Nathalie surname: Ly fullname: Ly, Nathalie organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – sequence: 5 givenname: Floriane E. surname: Braye fullname: Braye, Floriane E. organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – sequence: 6 givenname: Christophe surname: Zimmer fullname: Zimmer, Christophe organization: Institut Pasteur, Unité Imagerie et Modélisation, CNRS Unité de Recherche Associée 2582, 75015 Paris, France – sequence: 7 givenname: Florian surname: Mueller fullname: Mueller, Florian email: florian.muller@pasteur.fr organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France – sequence: 8 givenname: Xavier surname: Darzacq fullname: Darzacq, Xavier email: darzacq@berkeley.edu organization: Functional Imaging of Transcription, Ecole Normale Supérieure, Institut de Biologie de l’ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris 75005, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24981864$$D View this record in MEDLINE/PubMed https://hal.sorbonne-universite.fr/hal-01312884$$DView record in HAL |
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Publisher_xml | – name: Elsevier Inc – name: Elsevier |
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Snippet | Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chromatin environment is known to influence the bursting behavior... Transcription is a stochastic process occurring mostly in episodic bursts. Although the local chro-matin environment is known to influence the bursting... |
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SubjectTerms | Alleles Cell Line, Tumor Cells, Cultured Cellular Biology DNA-Directed RNA Polymerases - metabolism Humans Life Sciences Models, Genetic Protein Structure, Tertiary Proto-Oncogene Proteins c-fos - genetics Proto-Oncogene Proteins c-fos - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Stochastic Processes Transcription Factors - chemistry Transcription Factors - genetics Transcription Factors - metabolism Transcriptional Activation |
Title | Transcription Factors Modulate c-Fos Transcriptional Bursts |
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