TY - JOUR
T1 - Targeting GATA transcription factors – A novel strategy for anti-aging interventions?
AU - Zimmermann, Andreas
AU - Kainz, Katharina
AU - Hofer, Sebastian J.
AU - Bauer, Maria A.
AU - Schroeder, Sabrina
AU - Dengjel, Jörn
AU - Pietrocola, Federico
AU - Kepp, Oliver
AU - Ruckenstuhl, Christoph
AU - Eisenberg, Tobias
AU - Sigrist, Stephan J.
AU - Madeo, Frank
AU - Kroemer, Guido
AU - Carmona-Gutierrez, Didac
N1 - Publisher Copyright:
© 2019 Shared Science Publishers OG. All rights reserved.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - GATA transcription factors (TFs) constitute a conserved family of zinc-finger TFs that fulfill diverse functions across eukaryotes. Accumulating evidence suggests that GATA TFs also play a role in lifespan regulation. In a recent study, we identified a natural polyphenol, 4,4’-dimethoxychalcone (DMC), that extends lifespan depending on reduced activity of distinct GATA TFs. Prolonged lifespan by DMC treatment depends on autophagy, a protective cellular self-cleansing mechanism. In yeast, DMC reduces the activity of the GATA TF Gln3 and, genetic deletion of Gln3 is sufficient to increase autophagy levels during cellular aging. In addition, we observed similar changes in the abundance of several amino acids in the metabolome of DMC-treated and GATA/Gln3 depleted cells. Here, we examine current data on the involvement of GATA TFs in the regulation of autophagy and longevity in different organisms and explore if GATA TFs might be suitable targets for anti-aging interventions.
AB - GATA transcription factors (TFs) constitute a conserved family of zinc-finger TFs that fulfill diverse functions across eukaryotes. Accumulating evidence suggests that GATA TFs also play a role in lifespan regulation. In a recent study, we identified a natural polyphenol, 4,4’-dimethoxychalcone (DMC), that extends lifespan depending on reduced activity of distinct GATA TFs. Prolonged lifespan by DMC treatment depends on autophagy, a protective cellular self-cleansing mechanism. In yeast, DMC reduces the activity of the GATA TF Gln3 and, genetic deletion of Gln3 is sufficient to increase autophagy levels during cellular aging. In addition, we observed similar changes in the abundance of several amino acids in the metabolome of DMC-treated and GATA/Gln3 depleted cells. Here, we examine current data on the involvement of GATA TFs in the regulation of autophagy and longevity in different organisms and explore if GATA TFs might be suitable targets for anti-aging interventions.
KW - Amino acids
KW - Anti-aging
KW - Autophagy
KW - Flavonoids
KW - GATA
KW - Yeast
UR - http://www.scopus.com/inward/record.url?scp=85093882959&partnerID=8YFLogxK
U2 - 10.15698/mic2019.05.676
DO - 10.15698/mic2019.05.676
M3 - Article
AN - SCOPUS:85093882959
SN - 2311-2638
VL - 6
SP - 212
EP - 216
JO - Microbial Cell
JF - Microbial Cell
IS - 5
ER -