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A stochastic epigenetic switch controls the dynamics of T-cell lineage commitment
by
Ng, Kenneth KH
, Siu, Sharmayne
, Kueh, Hao Yuan
, Elowitz, Michael B
, Pease, Shirley
, Hirose, Satoshi
, Mehta, Arnav
, Yui, Mary A
, Rothenberg, Ellen V
, Irwin, Blythe
in
Animals
/ Bioengineering
/ Cell Differentiation
/ Cell fate
/ Cell lineage
/ Computational and Systems Biology
/ Deoxyribonucleic acid
/ Developmental Biology
/ DNA
/ DNA methylation
/ Epigenesis, Genetic
/ Epigenetics
/ Experiments
/ Gene expression
/ Gene loci
/ gene regulation
/ Genes, Reporter
/ Intravital Microscopy
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ lymphocyte development
/ Lymphocytes T
/ Mathematical models
/ Mice
/ Models, Theoretical
/ Proteins
/ quantitative and systems biology
/ Repressor Proteins - biosynthesis
/ Staining and Labeling
/ stochastic gene expression
/ T-Lymphocytes - physiology
/ Time Factors
/ Transcription activation
/ Transcription factors
/ Transcription, Genetic
/ Tumor Suppressor Proteins - biosynthesis
2018
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A stochastic epigenetic switch controls the dynamics of T-cell lineage commitment
by
Ng, Kenneth KH
, Siu, Sharmayne
, Kueh, Hao Yuan
, Elowitz, Michael B
, Pease, Shirley
, Hirose, Satoshi
, Mehta, Arnav
, Yui, Mary A
, Rothenberg, Ellen V
, Irwin, Blythe
in
Animals
/ Bioengineering
/ Cell Differentiation
/ Cell fate
/ Cell lineage
/ Computational and Systems Biology
/ Deoxyribonucleic acid
/ Developmental Biology
/ DNA
/ DNA methylation
/ Epigenesis, Genetic
/ Epigenetics
/ Experiments
/ Gene expression
/ Gene loci
/ gene regulation
/ Genes, Reporter
/ Intravital Microscopy
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ lymphocyte development
/ Lymphocytes T
/ Mathematical models
/ Mice
/ Models, Theoretical
/ Proteins
/ quantitative and systems biology
/ Repressor Proteins - biosynthesis
/ Staining and Labeling
/ stochastic gene expression
/ T-Lymphocytes - physiology
/ Time Factors
/ Transcription activation
/ Transcription factors
/ Transcription, Genetic
/ Tumor Suppressor Proteins - biosynthesis
2018
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A stochastic epigenetic switch controls the dynamics of T-cell lineage commitment
by
Ng, Kenneth KH
, Siu, Sharmayne
, Kueh, Hao Yuan
, Elowitz, Michael B
, Pease, Shirley
, Hirose, Satoshi
, Mehta, Arnav
, Yui, Mary A
, Rothenberg, Ellen V
, Irwin, Blythe
in
Animals
/ Bioengineering
/ Cell Differentiation
/ Cell fate
/ Cell lineage
/ Computational and Systems Biology
/ Deoxyribonucleic acid
/ Developmental Biology
/ DNA
/ DNA methylation
/ Epigenesis, Genetic
/ Epigenetics
/ Experiments
/ Gene expression
/ Gene loci
/ gene regulation
/ Genes, Reporter
/ Intravital Microscopy
/ Luminescent Proteins - analysis
/ Luminescent Proteins - genetics
/ lymphocyte development
/ Lymphocytes T
/ Mathematical models
/ Mice
/ Models, Theoretical
/ Proteins
/ quantitative and systems biology
/ Repressor Proteins - biosynthesis
/ Staining and Labeling
/ stochastic gene expression
/ T-Lymphocytes - physiology
/ Time Factors
/ Transcription activation
/ Transcription factors
/ Transcription, Genetic
/ Tumor Suppressor Proteins - biosynthesis
2018
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A stochastic epigenetic switch controls the dynamics of T-cell lineage commitment
Journal Article
A stochastic epigenetic switch controls the dynamics of T-cell lineage commitment
2018
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Overview
Cell fate decisions occur through the switch-like, irreversible activation of fate-specifying genes. These activation events are often assumed to be tightly coupled to changes in upstream transcription factors, but could also be constrained by cis-epigenetic mechanisms at individual gene loci. Here, we studied the activation of Bcl11b, which controls T-cell fate commitment. To disentangle cis and trans effects, we generated mice where two Bcl11b copies are tagged with distinguishable fluorescent proteins. Quantitative live microscopy of progenitors from these mice revealed that Bcl11b turned on after a stochastic delay averaging multiple days, which varied not only between cells but also between Bcl11b alleles within the same cell. Genetic perturbations, together with mathematical modeling, showed that a distal enhancer controls the rate of epigenetic activation, while a parallel Notch-dependent trans-acting step stimulates expression from activated loci. These results show that developmental fate transitions can be controlled by stochastic cis-acting events on individual loci.
Publisher
eLife Sciences Publications Ltd,eLife Sciences Publications, Ltd
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