Population kinetics and simulation of E2 induction. Related to Fig 4

Slides:



Advertisements
Similar presentations
Descriptive Statistics Review – Chapter 14. Data  Data – collection of numerical information  Frequency distribution – set of data with frequencies.
Advertisements

BIA 2610 – Statistical Methods Chapter 3 – Descriptive Statistics: Numerical Measures.
Fus3 is required for deletions of GIM4 and BIM1 to increase cell‐to‐cell variability Fus3 is required for deletions of GIM4 and BIM1 to increase cell‐to‐cell.
DNase‐HS sites are main independent determinants of DNA replication timing Simulations based on genome sequence features (GC content, CpG islands), or.
Abundance of proteins matching selected subcellular locations and functions in CaCo‐2 cells. Abundance of proteins matching selected subcellular locations.
Comparative Analysis of Single-Cell RNA Sequencing Methods
A kinetic model reconciles observed ERK phosphorylation, localization, and activity responses A Schematic of a simple kinetic model including cytosolic.
MRNA coexpression of neighbouring genes is driven by chromatin fluctuations and regulatory interference mRNA coexpression of neighbouring genes is driven.
Melting behavior of protein complexes
Characterization and quantification of clonal heterogeneity among hematopoietic stem cells: a model-based approach by Ingo Roeder, Katrin Horn, Hans-Bernd.
(A) Outline of the malignant transformation process.
Sensitivity of RNA‐seq.
Tight regulation of gene expression variation is coupled to promoter architecture. Tight regulation of gene expression variation is coupled to promoter.
Sampling Distribution
Sampling Distribution
Dual allele labeling reveals a trans‐acting source for extrinsic noise
Mononucleotide models describe sequence‐to‐shape relationships well
Comparative analysis of RNA and protein profiles.
Prediction of IGHV status based on Factor 1 in the CLL data and validation on outlier cases on independent assays Prediction of IGHV status based on Factor.
CAR T cell dose and percentages of CAR‐positive cells within CAR T cell products CAR T cell dose and percentages of CAR‐positive cells within CAR T cell.
Dose response of pAGA1 and pFIG1 induction
Isolation of transcription elongation complexes from the 5′ and 3′ regions of a single gene Isolation of transcription elongation complexes from the 5′
Comparing histone profiles and DNA accessibility of secretory and enterocyte progenitor cells Comparing histone profiles and DNA accessibility of secretory.
Intracellular noise in the cAMP circuit drives observed population behaviors Firing rate phase diagrams for single cells in a population (top) and the.
Characterization of promoters relative to pAGA1
Dynamics and variability of SMAD2 signaling in single cells
Evaluating CRISPR negative selection screens.
A coherent feed‐forward motif sharpens the Dnmt3b transcriptional output into a bistable switch. A coherent feed‐forward motif sharpens the Dnmt3b transcriptional.
Widespread Inhibition of Posttranscriptional Splicing Shapes the Cellular Transcriptome following Heat Shock  Reut Shalgi, Jessica A. Hurt, Susan Lindquist,
Downstream antagonism.
Differences in cellular organization emerge from quantitative proteomic experiments Differences in cellular organization emerge from quantitative proteomic.
Validation of some ePTL candidates.
Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+ cells Lysozyme expression in isolated Paneth cells and linage tracing of Notch1+
Collective shifts of abundance for nuclear and extracellular proteins in colorectal cancer Collective shifts of abundance for nuclear and extracellular.
Mean feature profiles of targeted cells are highly consistent between gRNA sequences Mean feature profiles of targeted cells are highly consistent between.
Effect of the loss of Kar4 on the induction of various promoters
Dynamics and expression level of mating‐dependent promoters
Validation of knock‐in cell line and image calibration (related to Fig 1)‏ Validation of knock‐in cell line and image calibration (related to Fig 1) Validation.
Francis Crick's central dogma of biology revolves around the transcription of mRNA from DNA, the translation of proteins from mRNA, and the degradation.
Knock‐in of PP7 stem‐loop sequences provides visualization of estrogen‐mediated transcription from the endogenous GREB1 locus in living cells (see also.
Antisense transcription, measurement, and correction
History dependence and robust species coexistence in pairwise consortia motifs History dependence and robust species coexistence in pairwise consortia.
Transcriptomic and epigenetic changes associated with Factor 1 in the scMT data Transcriptomic and epigenetic changes associated with Factor 1 in the scMT.
Calibration of a population‐average model
Comparison of proteomics and RNA‐Seq data.
Comparison of nuclear surface area of HeLa and RKO cells
Dynamics of induction of mating promoters after pheromone stimulation
Simulation showing that the cell length variability of the entire population can mask abnormal cell length variability at a specific cell cycle period.
Kinome‐wide activity regulation derived from known substrates and 41 quantitative phosphoproteomic studies Kinome‐wide activity regulation derived from.
An integrated NHR network.
Design and optimization of the computational model.
Proliferative advantage depends on environmental dynamics
RSLs enable internal replicate and lineage dropout analyses
Maintenance of lysogeny in bacteriophage lambda.
Construction of a genome‐scale pool of barcoded PCA strains
Effect of HDAC inhibition on the steady‐state and dynamic transcriptional response and associated noise. Related to Fig 7 Effect of HDAC inhibition on.
Noise in hoxb1a/krox20 expression leads to boundary sharpening.
Characterising dermis expansion and gene expression changes during mouse development (related to Fig 1)‏ Characterising dermis expansion and gene expression.
Antisense expression associates with larger gene expression variability. Antisense expression associates with larger gene expression variability. (A–D)
Characterization and model parameterization for CcaSR
Remodeling of the mitochondrial and extracellular proteome during Caenorhabditis elegans aging Remodeling of the mitochondrial and extracellular proteome.
Rare and abundant codons.
Functional metabolic rearrangements in chloramphenicol‐resistant populations Functional metabolic rearrangements in chloramphenicol‐resistant populations.
Single‐cell RT–qPCR data
The transcriptional behavior of GREB1 changes with estrogen dose and exhibits considerable cell‐to‐cell variation (see also Fig EV2 and Movie EV2)‏ The.
Sequence dependence of Met4 recruitment.
Kinetics of GREB1 induction by estrogen in single cells (see also Fig EV4 and Movie EV3)‏ Kinetics of GREB1 induction by estrogen in single cells (see.
Topologies, synthetic implementations and expression profiles of the networks studied Topologies, synthetic implementations and expression profiles of.
Cell‐specific responses to the cytokine TGFβ are determined by variability in protein levels Unimodal distribution of protein concentrations in artificial.
Enhancer Control of Transcriptional Bursting
Presentation transcript:

Population kinetics and simulation of E2 induction. Related to Fig 4 Population kinetics and simulation of E2 induction. Related to Fig 4 Variability of response times depends on the number of steps in the promoter cycle. Heterogeneity in response times was calculated as the coefficient of variation (CV) from simulations of E2 induction experiments. The distribution of CVs over all SMC ABC posterior particles from the fit to steady‐state dose‐response at 1,000 pM E2 (Fig 3) with models containing either two (left) or ten (right) states is shown as boxplots.The kinetics of E2 induction in single living cells is similar to ensemble RT–qPCR measurements. MCF7 cells were starved of E2 for 3 days and then induced with either 10 pM (left) or with 1,000 pM E2 (right) with samples being collected every 10 min for RT–qPCR. The location of the qPCR products and of the PP7 sequences is indicated on the schematic of the GREB1 gene structure. Primer pairs were designed to span exon–intron boundaries to exclusively amplify unspliced pre‐mRNA. The mean of three experiments is plotted with standard deviation shown as shaded areas. Response times and delay between amplicons are estimated from the time taken to achieve a threefold induction. The mean intensity of transcription sites from Fig 4A is shown in green and shows excellent agreement with population and single‐cell response.Minimal promoter models yield a better model fit for induction datasets. SMC ABC was performed with the 10 or 1,000 pM E2 induction datasets, while keeping the model topology fixed at a two‐state (1–1–5) or ten‐state (1–9–5) model. Distances of the final particle populations are shown as boxplots. For both experimental datasets, the two‐state model yields a smaller final distance value than the ten‐state model, indicating better description of the data.Promoter models with multiple states produce homogenous response times. Simulations of synchronized cells were performed with parameters derived from fits of the 10 pM induction dataset for a promoter cycle with 10 states (tON = 0.8 min; tOFF = 30 min; b = 6 RNAs/burst, model topology: 1–9–5). The median and CV of response times are indicated in red.Data information: (A, C) Description of boxplots: central line, median; box, 25 and 75% percentile; whiskers, 5 and 95% percentile. Christoph Fritzsch et al. Mol Syst Biol 2018;14:e7678 © as stated in the article, figure or figure legend