Name: Comparing Budding Curves, Flow Cytometry Data, and Experimental Data
Uploaded: 2023-06-09T13:00:00
Description: Watch this Scientific Journal Video about Comparing Budding Curves, Flow Cytometry Data, and Experimental Data at JoVE.com

comparing budding curves, flow cytometry data, and experimental data

Alignement des données de séries chronologiques synchronisées pour les comparaisons entre expériences

Time-series measurements made on synchronized populations of cells as they progress through the cell cycle is a standard method for investigating the mechanisms that control cell-cycle progression1,2,3,4,5,6,7,8. The ability to make comparisons across synchrony/release time-series experiments is vital to our understanding of these dynamic processes. The use of replicate experiments to corroborate findings can increase the confidence in the reproducibility of the conclusions. Furthermore, comparisons between environmental conditions, across mutants, and even between species can uncover many new insights into cell-cycle regulation. However, interexperimental variability in the recovery from synchrony and in the speed of cell-cycle progression impairs the ability to make time-point-to-time-point comparisons across replicates or between experiments with altered cell-cycle timing. Due to these challenges, replicates are often not included for the full time series (e.g., Spellman et al.4). When replicates for the entire time series are gathered, the data cannot be analyzed in aggregate, but rather a single replicate is used for analysis, and other replicates are often relegated to supplemental figures (e.g., Orlando et al.8). Furthermore, comparisons between experiments with different recovery or cell-cycle progression characteristics are difficult. The measurements of smaller intervals between an event of interest and a cell-cycle landmark (e.g., bud emergence, S-phase entry, or anaphase onset) can help reduce errors if these landmark events are tracked1,2,3,9,10,11,12. However, subtle but important differences may remain undetected or obscured using these ad hoc methods. Finally, single-cell analyses allow for analyzing cell-cycle progression without relying on synchronization or alignment13, though large-scale measurements in single-cell studies can be challenging and costly.
To overcome these difficulties, we developed the Characterizing Loss of Cell Cycle Synchrony (CLOCCS) model to aid the analysis of time-series measurements made on synchronized populations14,15. CLOCCS is a flexible mathematical model that describes the distribution of synchronized cells across cell-cycle phases as they are released from synchrony and progress through the cell cycle. The branching process framework enables the model to account for the asymmetric qualities of mother and daughter cells after division, as observed in S. cerevisiae, while still being useful for organisms that divide by fission, such as S. pombe. The model can take inputs from a diverse set of measurement types to specify the cell-cycle phase. It can ingest budding cell-cycle phase data, which includes measurements of the percent budded cells over time, allowing for the estimation of the number of cells outside of the unbudded G1 phase14,15. The model can also ingest flow cytometric data that measures the DNA content, thus enabling the assessment of landmark transitions from G1 to S, S to G2, and M to G115. Fluorescent morphological markers can also be used to identify the cell-cycle phase. The fluorescent labeling of myosin rings, nuclei, and spindle pole bodies (SPBs) can be used to determine the cell-cycle phase, and these were incorporated into the CLOCCS model11; however, these measurements will not be described in this protocol. Additionally, the septation index was used as an input for modeling data from S. pombe14. Thus, the model can be used for cell-cycle analyses in a variety of organisms and can be further expanded.
CLOCCS is a parametric model that allows for the full Bayesian inference of multiple parameters from the input data (e.g., budding percentage, DNA content). These parameters include the recovery time from synchrony, the length of the cell-cycle period (estimated separately for mother and daughter cells), and the average cell-cycle position of the cells at each time point. These parameters represent the behavior of the average cell in the population, enabling the researcher to map each time point to a cell-cycle position expressed as a lifeline point. The conversion to lifeline points depends on the CLOCCS parameters lambda (&#955;) and mu0 (&#181;0)14,15. The parameter &#955; corresponds to the average cell-cycle period of the mother cells. However, due to the mother-daughter delay14,15, this is not the average cell-cycle period of the full population that includes both the mother and daughter cells. CLOCCS additionally infers the parameter delta (&#948;), which corresponds to the mother-daughter delay and, thus, allows for the calculation of the average cell-cycle period of the full population. Finally, because each experiment begins after release from cell-cycle synchronization, the time required to recover from the synchronization method is represented by the CLOCCS parameter &#181;0. CLOCCS fits a model to the input cell-cycle phase data and then infers these parameters using a random walk Markov chain Monte Carlo algorithm14,15. By mapping multiple experiments to a common cell-cycle lifeline time scale, direct phase-specific comparisons can be made between replicates or experiments where the recovery time or cell-cycle periods are not identical8,14,15.
As synchronized populations lose synchrony at some rate over the course of the time series14,15,16,17, variability in the rate of synchrony loss can also impede quantitative comparisons across experiments. By identifying the location of populations and the variance in their distributions, CLOCCS accounts for differences in rates of synchrony loss. This powerful tool allows for specific and detailed comparisons across experiments, thus providing the ability to directly make relevant comparisons not only between replicates but also between environmental conditions, mutants, and even species that have dramatically different cell-cycle timing14,15.
This paper describes a method using CLOCCS to estimate parameters by fitting data from synchrony/release time-series experiments, map the data to a common lifeline scale, and then make relevant comparisons between replicates or experiments. Lifeline alignment allows for direct phase-specific comparisons across these experiments, which allows for the aggregation and comparison of replicates and for making more relevant comparisons across experiments with different recovery timings and cell-cycle periods.

Pleins feux sur l’auteur : Alignement de données de séries chronologiques synchronisées à l’aide du modèle de caractérisation de la perte de synchronisation du cycle cellulaire pour les comparaisons i

Alignement de données de séries chronologiques synchronisées à l’aide du modèle de synchronisation de perte de cycle cellulaire caractérisant pour les comparaisons entre expériences

A major challenge of analyzing time-series experiments is that they often differ in the length of recovery from synchrony and the cell cycle period. So measurements from different experiments cannot readily be compared or analyzed in aggregate without alignment. Clocks lifeline alignment is a method for phase specific and biologically relevant comparisons between experiments and for aggregating multiple replicate experiments both of which were previously difficult or impossible.Previously phase specific and biologically relevant comparisons were made by tracking landmark events. However, using these ad hoc methods, subtle but important differences remain undetected. Comparison between time series experiments is particularly difficult between experiments with significant differences in timing such as in mutant populations or growth conditions that affect the synchrony recovery time or the cell cycle period.Clocks lifeline alignment allows for phase specific comparison in these cases. We have used clocks to align time series transcriptomic and proteomic data, which allowed for the direct comparison between the dynamics of the mRNA and the corresponding protein. Furthermore, we align time series experiments across different species, providing critical insights into cell cycle evolutionary changes.

Watch this Scientific Journal Video about Comparing Budding Curves, Flow Cytometry Data, and Experimental Data at JoVE.com

Comparing Budding Curves, Flow Cytometry Data, and Experimental Data  

Comparaison des courbes bourgeonnantes, des données de cytométrie en flux et des données expérimentales

Tracez les courbes bourgeonnantes avant l’alignement à l’aide de la fonction utilitaire Python en entrant la commande dans une nouvelle cellule. Ensuite, tracez les courbes bourgeonnantes après l’alignement. Utilisation de la fonction utilitaire Python.Utilisez la comparaison de graphiques linéaires fournie dans le flacon d’utilitaires Python pour effectuer des comparaisons de graphiques linéaires sur le bloc de données original, aligné ou aligné et interpolé. En tapant la commande dans une nouvelle cellule, importez un fichier de liste de gènes CSV ou TSV dans le bloc-notes à l’aide de la commande dans une nouvelle cellule. Ensuite, utilisez la comparaison de carte thermique de tracé de fonction fournie dans le fichier d’utilitaires Python pour effectuer une comparaison de carte thermique sur le bloc de données interpolé aligné et aligné en phase en tapant la commande dans une nouvelle cellule.Une comparaison des données transcriptomatiques alignées et non alignées a montré qu’avant l’alignement, le premier pic d’expression des expériences de microréseaux semblait aligné avec le deuxième pic de l’expérience RNA-seq. Cependant, après l’alignement, les premiers pics du cycle cellulaire de chaque jeu de données sont correctement alignés. La comparaison des données de phase du cycle cellulaire entre des expériences avec des périodes variables a montré des différences de période visibles dans les courbes bourgeonnantes non alignées.Alors que l’alignement des horloges rendait les trois courbes remarquablement similaires, ce qui rendait possible la comparaison des données expérimentales, les données de phase du cycle cellulaire pour chaque point de ligne de vie comparable n’étaient pas identiques entre les deux conditions. La comparaison des données transcriptomiques entre des expériences avec des périodes variables a montré qu’avant l’alignement, la dynamique de transcription de CDC20 ne se chevauchait pas. Mais après l’alignement, les pics se sont produits sur la même phase du cycle cellulaire, mais les formes des courbes étaient différentes.Les gènes ont été tracés sous forme de cartes thermiques dans le même ordre pour les trois conditions pour les non-alignés et les alignés.

Research

JoVE Journal

Biology

Comparing Budding Curves, Flow Cytometry Data, and Experimental Data

Alignment of Synchronized Time-Series Data Using the Characterizing Loss of Cell Cycle Synchrony Model for Cross-Experiment Comparisons

Investigating the cell cycle often depends on synchronizing cell populations to measure various parameters in a time series as the cells traverse the cell ...

Recherche

Biologie

Installing CLOCCS and Using it to Parameterize the Experiments

Installation de CLOCCS et utilisation de celui-ci pour paramétrer les expériences

Conversion of Time Points to Lifeline Points Using the Python Conversion Functions and the CLOCCS Parameters

Conversion de points temporels en points de ligne de vie à l’aide des fonctions de conversion Python et des paramètres CLOCCS