scholarly journals Exact Bayesian lineage tree-based inference identifies Nanog negative autoregulation in mouse embryonic stem cells

2016 ◽  
Author(s):  
Justin Feigelman ◽  
Stefan Ganscha ◽  
Simon Hastreiter ◽  
Michael Schwarzfischer ◽  
Adam Filipczyk ◽  
...  

AbstractThe autoregulatory motif of Nanog, a heterogeneously expressed core pluripotency factor in mouse embryonic stem cells, remains debated. Although recent time-lapse microscopy data provide the unparalleled ability to monitor Nanog expression at the single-cell level, the extraction of mechanistic knowledge is precluded by the lack of inference techniques suitable for noisy, incomplete and heterogeneous data obtained from proliferating cell populations.This work identifies Nanog’s autoregulatory motif from quantified time-lapse fluorescence line-age trees with STILT (Stochastic Inference on Lineage Trees), a novel particle-filter based algorithm for exact Bayesian parameter inference and model selection of stochastic models. We first verify STILT’s ability to accurately infer parameters and select the correct autoregulatory motif from simulated data. We then apply STILT to time-lapse microscopy movies of a fluorescent Nanog fusion protein reporter and reject the possibility of positive autoregulation. Finally, we use STILT for experimental design, perform in silico overexpression simulations, and experimentally validate model predictions via exogenous Nanog overexpression. We finally conclude that the protein expression dynamics and overexpression experiments strongly suggest a weak negative feedback from the protein on the DNA activation rate.We find that a simple autoregulatory mechanism can explain the observed heterogeneous Nanog dynamics. This finding has implications on the understanding of the core pluripotency network, such as supporting the ability of mESC populations to diversify their proteomic profile to respond to a spectrum of differentiation cues. Beyond this application STILT constitutes a generally applicable fully Bayesian approach for model selection of gene regulatory models on the basis of time-lapse imaging data of proliferating cell populations. STILT is freely available at: http://www.imsb.ethz.ch/research/claassen/Software/stilt—stochastic-inference-on-lineage-trees.html

2020 ◽  
Vol 133 (20) ◽  
pp. jcs255166

ABSTRACTFirst Person is a series of interviews with the first authors of a selection of papers published in Journal of Cell Science, helping early-career researchers promote themselves alongside their papers. Federico Pecori is first author on ‘Mucin-type O-glycosylation controls pluripotency in mouse embryonic stem cells via Wnt receptor endocytosis’, published in JCS. Federico is a PhD student in the lab of Shoko Nishihara at the Laboratory of Cell Biology, Department of Bioinformatics, Soka University, Tokyo, Japan, where he is interested in the mechanisms regulating stem cell identity.


2015 ◽  
Vol 14 (2) ◽  
pp. 224-237 ◽  
Author(s):  
Mathilde Couteaudier ◽  
Laëtitia Trapp-Fragnet ◽  
Nicolas Auger ◽  
Katia Courvoisier ◽  
Bertrand Pain ◽  
...  

2011 ◽  
Vol 195 (6) ◽  
pp. 507-523 ◽  
Author(s):  
Insa S. Schroeder ◽  
Sabine Sulzbacher ◽  
Tobias Nolden ◽  
Joerg Fuchs ◽  
Judith Czarnota ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (9) ◽  
pp. e44912 ◽  
Author(s):  
Elke Gabriel ◽  
Stephanie Schievenbusch ◽  
Eugen Kolossov ◽  
Jan G. Hengstler ◽  
Tamara Rotshteyn ◽  
...  

Stem Cells ◽  
2008 ◽  
Vol 26 (9) ◽  
pp. 2245-2256 ◽  
Author(s):  
Irina Drobinskaya ◽  
Thomas Linn ◽  
Tomo Šarić ◽  
Reinhard G. Bretzel ◽  
Heribert Bohlen ◽  
...  

2002 ◽  
Vol 2 ◽  
pp. 690-700 ◽  
Author(s):  
Joy Rathjen ◽  
Peter D. Rathjen

Recent interest in the generation of neural lineages by differentiation of embryonic stem cells arises from the opportunities represented by a developmentally normal, unlimited source of material that can be manipulated genetically with precision. Several experimental approaches, which differ conceptually, in the route of differentiation and the characteristics of the resulting cell population have been reported. In this review we undertake a comparative analysis of these approaches and their suitability for experimental investigation or implantation.


2005 ◽  
Vol 92 (7) ◽  
pp. 920-933 ◽  
Author(s):  
Magnus Schroeder ◽  
Sylvia Niebruegge ◽  
Andreas Werner ◽  
Elmar Willbold ◽  
Monika Burg ◽  
...  

2021 ◽  
Vol 3 ◽  
Author(s):  
Mohammed Abdulhasan ◽  
Ximena Ruden ◽  
Yuan You ◽  
Sean M. Harris ◽  
Douglas M. Ruden ◽  
...  

Fluorescent ubiquitination-based cell cycle indicator (FUCCI) embryonic stem cells (ESCs), which fluoresce green during the S-G2-M phases, generate an S-shaped curve for the accumulation of cells during normal stemness (NS) culture with leukemia-inhibitory factor (LIF). Since it was hypothesized that a culture of ESCs was heterogeneous in the cell cycle, it was expected that increased S-G2-M-phases of the cell cycle would make an S-shaped curve parallel to the accumulation curve. Unexpectedly, it was observed that the fraction of FUCCI ESCs in green decreases over time to a nadir at ∼24 h after previous feeding and then rapidly enters S-G2-M-phases after medium change. G1 delay by infrequent medium change is a mild stress, as it does not affect growth significantly when frequency is increased to 12 h. Perfluoro-octanoic acid (PFOA) and diethyl phthalate (DEP) were used as examples of members of the per- and polyfluoroalkyl substances (PFAS) and phthalate families of chemicals, respectively. Two adverse outcomes were used to compare dose- and time-dependent effects of PFOA and DEP. The first was cell accumulation assay by time-lapse confluence measurements, largely at Tfinal/T74 h. The second was by quantifying dominant toxicant stress shown by the suppression of mild stress that creates a green fed/unfed peak. In terms of speed, PFOA is 26 times faster than DEP for producing a time-dependent LOAEL dose at 100 uM (that is, 2 h for PFOA and 52 h for DEP). PFOA has 1000-fold more sensitive LOAEL doses than DEP for suppressing ESC accumulation (confluence) at day 3 and day 2. There were two means to compare the magnitude of the growth suppression of PFOA and DEP. For the suppression of the accumulation of cells measured by confluence at Tfinal/T74h, there was a 13-fold suppression at the highest dose of PFOA > the highest dose of DEP. For the suppression of entry into the cell cycle after the G1 phase by stress on day 1 and 2, there is 10-fold more suppression by PFOA than DEP. The data presented here suggest that FUCCI ESCs can assay the suppression of accumulated growth or predict the suppression of future growth by the suppression of fed/unfed green fluorescence peaks and that PFOA’s adverse effects are faster and larger and can occur at more sensitive lower doses than DEP.


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