scholarly journals Mathematical Modeling of the Eukaryotic Heat-Shock Response: Dynamics of the hsp70 Promoter

2005 ◽  
Vol 88 (3) ◽  
pp. 1646-1658 ◽  
Author(s):  
Theodore R. Rieger ◽  
Richard I. Morimoto ◽  
Vassily Hatzimanikatis
Small ◽  
2021 ◽  
pp. 2102145
Author(s):  
Nadia Vertti‐Quintero ◽  
Simon Berger ◽  
Xavier Casadevall i Solvas ◽  
Cyril Statzer ◽  
Jillian Annis ◽  
...  

Small ◽  
2021 ◽  
Vol 17 (30) ◽  
pp. 2170157
Author(s):  
Nadia Vertti‐Quintero ◽  
Simon Berger ◽  
Xavier Casadevall i Solvas ◽  
Cyril Statzer ◽  
Jillian Annis ◽  
...  

2019 ◽  
Author(s):  
Nadia Vertti-Quintero ◽  
Simon Berger ◽  
Xavier Casadevall i Solvas ◽  
Cyril Statzer ◽  
Jillian Annis ◽  
...  

AbstractGenetics, environment, and stochasticity influence the rate of ageing in living organisms. Individual Caenorhabditis elegans that are genetically identical and cultured in the same environment have different lifespans, suggesting a significant role of stochasticity in ageing. We have developed a novel microfluidic methodology to measure heat-shock response as a surrogate marker for heterogeneity associated with lifespan and have quantified the heat-shock response of C. elegans at the population, single individual, and tissue levels. We have further mathematically modelled our data to identify the major drivers determining such heterogeneity. This approach demonstrates that protein translation and degradation rate constants explain the individuality of the heat-shock time-course dynamic. We observed a decline of protein turnover capacity in early adulthood, co-incidentally occurring as the predicted proteostasis collapse. We identified a decline of intestinal response as the tissue that underlies the individual heterogeneity. Additionally, we verified that individuals with enhanced translation fidelity in early adulthood live longer. Altogether, our results reveal that the stochastic onset of proteostasis collapse of somatic tissues during early adulthood reflects individual protein translation capacity underlying heterogenic ageing of isogenic C. elegans.


PLoS ONE ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. e0129329 ◽  
Author(s):  
Andrea V. Gómez ◽  
Gonzalo Córdova ◽  
Roberto Munita ◽  
Guillermo E. Parada ◽  
Álvaro P. Barrios ◽  
...  

2001 ◽  
Vol 356 (2) ◽  
pp. 353-359 ◽  
Author(s):  
Alfredo MOLINA ◽  
Emmanuel Di MARTINO ◽  
Joseph A. MARTIAL ◽  
Marc MULLER

We reported previously that a tilapia (Oreochromis mossambicus) heat shock protein 70 (HSP70) promoter is able to confer heat shock response on a reporter gene after transient expression both in cell culture and in microinjected zebrafish embryos. Here we present the first functional analysis of a fish HSP70 promoter, the tiHSP70 promoter. Using transient expression experiments in carp EPC (epithelioma papulosum cyprini) cells and in microinjected zebrafish embryos, we show that a distal heat shock response element (HSE1) at approx. −800 is predominantly responsible for the heat shock response of the tiHSP70 promoter. This element specifically binds an inducible transcription factor, most probably heat shock factor, and a constitutive factor. The constitutive complex is not observed with the non-functional, proximal HSE3 sequence, suggesting that both factors are required for the heat shock response mediated by HSE1.


2009 ◽  
Vol 37 (1) ◽  
pp. 123-126 ◽  
Author(s):  
Charlotte R. Cooper ◽  
Amanda J. Daugherty ◽  
Sabrina Tachdjian ◽  
Paul H. Blum ◽  
Robert M. Kelly

TA (toxin–antitoxin) loci are ubiquitous in prokaryotic micro-organisms, including archaea, yet their physiological function is largely unknown. For example, preliminary reports have suggested that TA loci are microbial stress-response elements, although it was recently shown that knocking out all known chromosomally located TA loci in Escherichia coli did not have an impact on survival under certain types of stress. The hyperthermophilic crenarchaeon Sulfolobus solfataricus encodes at least 26 vapBC (where vap is virulence-associated protein) family TA loci in its genome. VapCs are PIN (PilT N-terminus) domain proteins with putative ribonuclease activity, while VapBs are proteolytically labile proteins, which purportedly function to silence VapCs when associated as a cognate pair. Global transcriptional analysis of S. solfataricus heat-shock-response dynamics (temperature shift from 80 to 90°C) revealed that several vapBC genes were triggered by the thermal shift, suggesting a role in heat-shock-response. Indeed, knocking out a specific vapBC locus in S. solfataricus substantially changed the transcriptome and, in one case, rendered the crenarchaeon heat-shock-labile. These findings indicate that more work needs to be done to determine the role of VapBCs in S. solfataricus and other thermophilic archaea, especially with respect to post-transcriptional regulation.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Brian D Alford ◽  
Eduardo Tassoni-Tsuchida ◽  
Danish Khan ◽  
Jeremy J Work ◽  
Gregory Valiant ◽  
...  

Understanding cellular stress response pathways is challenging because of the complexity of regulatory mechanisms and response dynamics, which can vary with both time and the type of stress. We developed a reverse genetic method called ReporterSeq to comprehensively identify genes regulating a stress-induced transcription factor under multiple conditions in a time-resolved manner. ReporterSeq links RNA-encoded barcode levels to pathway-specific output under genetic perturbations, allowing pooled pathway activity measurements via DNA sequencing alone and without cell enrichment or single-cell isolation. We used ReporterSeq to identify regulators of the heat shock response (HSR), a conserved, poorly understood transcriptional program that protects cells from proteotoxicity and is misregulated in disease. Genome-wide HSR regulation in budding yeast was assessed across 15 stress conditions, uncovering novel stress-specific, time-specific, and constitutive regulators. ReporterSeq can assess the genetic regulators of any transcriptional pathway with the scale of pooled genetic screens and the precision of pathway-specific readouts.


Author(s):  
Brian D. Alford ◽  
Gregory Valiant ◽  
Onn Brandman

AbstractInterrogating cellular stress response pathways is challenging because of the complexity of regulatory mechanisms and response dynamics, which can vary with both time and the type of stress. We developed a reverse genetic method called ReporterSeq to comprehensively identify genes regulating a stress-induced transcription factor under multiple conditions in a time-resolved manner. ReporterSeq links RNA-encoded barcode levels to pathway-specific output under genetic perturbations, allowing pooled pathway activity measurements via DNA sequencing alone and without cell enrichment or single cell isolation. Here, we used ReporterSeq to identify regulators of the heat shock response (HSR), a conserved, poorly understood transcriptional program that protects cells from proteotoxicity and is misregulated in disease. We measured genome-wide HSR regulation in budding yeast across thirteen stress conditions, uncovering novel stress-specific, time-specific, and constitutive regulators. ReporterSeq can assess the genetic regulators of any transcriptional pathway with the scale of pooled genetic screens and the precision of pathway-specific readouts.


2015 ◽  
Vol 109 (2) ◽  
pp. 182-193 ◽  
Author(s):  
Jeremy D. Scheff ◽  
Jonathan D. Stallings ◽  
Jaques Reifman ◽  
Vineet Rakesh

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