scholarly journals Dual Role of the Histone Variant H2A.Z in Transcriptional Regulation of Stress-Response Genes

2017 ◽  
Vol 29 (4) ◽  
pp. 791-807 ◽  
Author(s):  
Weronika Sura ◽  
Michał Kabza ◽  
Wojciech M. Karlowski ◽  
Tomasz Bieluszewski ◽  
Marta Kus-Slowinska ◽  
...  
2002 ◽  
Vol 277 (31) ◽  
pp. 27903-27911 ◽  
Author(s):  
Vasudevan Seshadri ◽  
Paul L. Fox ◽  
Chinmay K. Mukhopadhyay

2010 ◽  
Vol 8 (3) ◽  
pp. 67-80 ◽  
Author(s):  
Aleksey A Moskalev ◽  
Olga A Malysheva

It was investigated the role of stress-response genes (dFOXO, dSir2, Hsp70) in regulation of life span of Drosophila in response to light regime alteration. It was revealed the FOXO-dependant mechanism of lifespan increasing at darkness conditions. The distance of lifespan of FOXO homozygous mutants at different light conditions were absent 3 times from 4 times. It was shown, that homozygotes with deletion of dSir2 have more significant difference between lifespan at standard light and darkness conditions with comparing to wild type and heterozygous strain. The same tendency was also detected the in the strains with Hsp70 deletions. It was produced the evidences of two mechanisms of light regime influence on lifespan: metabolism intensification at light conditions and neuroendocrine-determinated lifespan increasing at darkness conditions.


Oncotarget ◽  
2016 ◽  
Vol 7 (39) ◽  
pp. 64124-64135 ◽  
Author(s):  
Sarrabeth Stone ◽  
Yeung Ho ◽  
Xiting Li ◽  
Stephanie Jamison ◽  
Heather P. Harding ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. e0120651 ◽  
Author(s):  
Alejandro Carozzo ◽  
Federico Diez ◽  
Natalia Gomez ◽  
Maia Cabrera ◽  
Carina Shayo ◽  
...  

2018 ◽  
Vol 131 (9) ◽  
pp. jcs204750 ◽  
Author(s):  
Peter Hoch-Kraft ◽  
Robin White ◽  
Stefan Tenzer ◽  
Eva-Maria Krämer-Albers ◽  
Jacqueline Trotter ◽  
...  

2007 ◽  
Vol 35 (4) ◽  
pp. 1245-1256 ◽  
Author(s):  
S. Renaud ◽  
D. Loukinov ◽  
Z. Abdullaev ◽  
I. Guilleret ◽  
F. T. Bosman ◽  
...  

Author(s):  
Malte Silomon ◽  
Inge Bauer ◽  
Michael Bauer ◽  
Julia Nolting ◽  
Markus Paxian ◽  
...  

AbstractStress response genes including heat shock proteins are induced under a variety of conditions to confer cellular protection. This study investigated the role of calcium signaling in the induction of two stress response genes, heme oxygenase-1/hsp32 and hsp70, in isolated rat hepatocytes. Both genes were induced by cellular glutathione depletion. This induction could be inhibited by BAPTA-AM. Culturing in a calcium-free medium prevented the induction of hsp70 gene expression after glutathione depletion without affecting heme oxygenase-1 gene expression. Thapsigargin increased the gene expression of heme oxygenase-1 but not that of hsp70. Thapsigargin-induced heme oxygenase-1 induction was completely inhibited by BAPTA-AM. Incubation with the Ca2+-ionophore A23187 augmented heme oxygenase-1 (two-fold) and hsp70 (5.2-fold) mRNA levels. Our data suggests a significant role of Ca2+-dependent pathways in the induction of the two stress genes. An increase in the cytoplasmic Ca2+ activity seems to play a key role in the cascade of signaling leading to the induction of the two genes. However, the source of Ca2+ that fluxes into the cytoplasm seems to be different. Our data provides evidence for a compartmentalization of calcium fluxes, i.e. the Ca2+ flux from intracellular stores (e.g. the endoplasmic reticulum) plays a major role in the induction of heme oxygenase-1. By contrast, Ca2+ flux from the extracellular medium seems to be a mechanism initiating the cellular signaling cascade leading to hsp70 gene induction.


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