scholarly journals Magnesium depletion extends fission yeast lifespan via general amino acid control activation

2021 ◽  
Vol 10 (2) ◽  
Author(s):  
Hokuto Ohtsuka ◽  
Mikuto Kobayashi ◽  
Takafumi Shimasaki ◽  
Teppei Sato ◽  
Genki Akanuma ◽  
...  
1987 ◽  
Vol 15 (13) ◽  
pp. 5261-5273 ◽  
Author(s):  
Kemin Zhou ◽  
Paula R.G. Brisco ◽  
Ari E. Hinkkanen ◽  
Gunter B. Kohlhaw

PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e27772 ◽  
Author(s):  
Irem Uluisik ◽  
Alaattin Kaya ◽  
Dmitri E. Fomenko ◽  
Huseyin C. Karakaya ◽  
Bradley A. Carlson ◽  
...  

2010 ◽  
Vol 285 (22) ◽  
pp. 16893-16911 ◽  
Author(s):  
Kirk A. Staschke ◽  
Souvik Dey ◽  
John M. Zaborske ◽  
Lakshmi Reddy Palam ◽  
Jeanette N. McClintick ◽  
...  

Genome ◽  
1988 ◽  
Vol 30 (6) ◽  
pp. 984-986 ◽  
Author(s):  
W. Xiao ◽  
G. H. Rank

The yeast ILV2 gene encodes acetolactate synthase, the first enzyme in the biosynthesis of isoleucine and valine. Its multiple regulation has precluded the clear demonstration of whether ILV2 is under general amino acid control. Nonderepressible gcn4 strains were used as recipients for transformation with a YCp plasmid carrying GCN4. Parental gcn4 cells and their isogenic GCN4 transformants were evaluated for ALS derepression following induced amino acid starvation. GCN4 cells showed 1.5-to 1.7-fold derepression but no derepression was observed in isogenic control gcn4 strains. A similar depression of ILV2 mRNA was also observed. Genetic evidence for general amino acid control was the gcn4 suppression of high level resistance to sulfometuron methyl by the SMR1-410 allele of ILV2.Key words: Saccharomyces cerevisiae, ILV2 gene, general amino acid control, multiple regulators.


1985 ◽  
Vol 5 (11) ◽  
pp. 3139-3148 ◽  
Author(s):  
M Crabeel ◽  
R Huygen ◽  
K Verschueren ◽  
F Messenguy ◽  
K Tinel ◽  
...  

To characterize further the regulatory mechanism modulating the expression of the Saccharomyces cerevisiae ARG3 gene, i.e., the specific repression by arginine and the general amino acid control, we analyzed by deletion the region upstream of that gene, determined the nucleotide sequence of operator-constitutive-like mutations affecting the specific regulation, and examined the behavior of an ARG3-galK fusion engineered at the initiating codon of ARG3. Similarly to what was observed in previous studies on the HIS3 and HIS4 genes, our data show that the general regulation acts as a positive control and that a sequence containing the nucleotide TGACTC, between positions -364 and -282 upstream of the transcription start, functions as a regulatory target site. This sequence contains the most proximal of the two TGACTC boxes identified in front of ARG3. While the general control appears to modulate transcription efficiency, the specific repression by arginine displays a posttranscriptional component (F. Messenguy and E. Dubois, Mol. Gen. Genet. 189:148-156, 1983). Our deletion and gene fusion analyses confirm that the specific and general controls operate independently of each other and assign the site responsible for arginine-specific repression to between positions -170 and +22. In keeping with this assignment, the two operator-constitutive-like mutations were localized at positions -80 and -46, respectively, and thus in a region which is not transcribed. We discuss a hypothesis accounting for the involvement of untranscribed DNA in a posttranscriptional control.


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