The PIF1 and MRS2 gene products have previously been shown to be essential for mitochondrial DNA maintenance at elevated temperatures and mitochondrial group II intron splicing, respectively, in the yeast Saccharomyces cerevisiae. A multicopy suppressor capable of rescuing the respiratory deficient phenotype associated with null alleles of either gene has been isolated. This suppressor is a nuclear gene that was called RIM2/MRS12. The RIM2/MRS12 gene encodes a predicted protein of 377 amino acids that is essential for mitochondrial DNA metabolism and proper cell growth. Inactivation of this gene causes the total loss of mitochondrial DNA and, compared to wild-type rho degrees controls, a slow-growth phenotype on media containing glucose. An...
A nuclear mutation, mgm101, results In temperature sensitive loss of mitochondrial DNA (mtDNA) in th...
Base substitutions equivalent to those causing human pathologies have been introduced in yeast mitoc...
A peculiar form of hepatocerebral mtDNA depletion syndrome is caused by mutations in the MPV17 gene,...
The PIF1 and MRS2 gene products have previously been shown to be essential for mitochondrial DNA mai...
The PIF1 and MRS2 gene products have previously been shown to be essential for mitochondrial DNA mai...
Disruption of the nuclear MRS2 gene (mrs2-1 mutation) causes a strong pet- phenotype in strains with...
Many human diseases including development of cancer is associated with depletion of mitochondrial DN...
Mitochondrial (mt) tRNA gene mutations are an important cause of human morbidity and are associated ...
It has previously been shown that the mitochondrial DNA (mtDNA) of Saccharomyces cerevisiae becomes ...
Mitochondria are essential for regulation of cellular respiration, energy production, small molecule...
MRP13 was defined by biochemical criteria as a 35-kilodalton small subunit protein of the yeast mito...
We utilized the heat-sensitive mutant strain (Ts932), bearing a mutation at position 61 in the mitoc...
RPM2 is identified here as a high-copy suppressor of isp42-3, a temperature-sensitive mutant allele ...
The mitochondrial protein synthesis presents specific features and uses specific components differen...
The yeast nuclear gene MRS2 encodes a protein of 54 kDa, the presence of which has been shown to be ...
A nuclear mutation, mgm101, results In temperature sensitive loss of mitochondrial DNA (mtDNA) in th...
Base substitutions equivalent to those causing human pathologies have been introduced in yeast mitoc...
A peculiar form of hepatocerebral mtDNA depletion syndrome is caused by mutations in the MPV17 gene,...
The PIF1 and MRS2 gene products have previously been shown to be essential for mitochondrial DNA mai...
The PIF1 and MRS2 gene products have previously been shown to be essential for mitochondrial DNA mai...
Disruption of the nuclear MRS2 gene (mrs2-1 mutation) causes a strong pet- phenotype in strains with...
Many human diseases including development of cancer is associated with depletion of mitochondrial DN...
Mitochondrial (mt) tRNA gene mutations are an important cause of human morbidity and are associated ...
It has previously been shown that the mitochondrial DNA (mtDNA) of Saccharomyces cerevisiae becomes ...
Mitochondria are essential for regulation of cellular respiration, energy production, small molecule...
MRP13 was defined by biochemical criteria as a 35-kilodalton small subunit protein of the yeast mito...
We utilized the heat-sensitive mutant strain (Ts932), bearing a mutation at position 61 in the mitoc...
RPM2 is identified here as a high-copy suppressor of isp42-3, a temperature-sensitive mutant allele ...
The mitochondrial protein synthesis presents specific features and uses specific components differen...
The yeast nuclear gene MRS2 encodes a protein of 54 kDa, the presence of which has been shown to be ...
A nuclear mutation, mgm101, results In temperature sensitive loss of mitochondrial DNA (mtDNA) in th...
Base substitutions equivalent to those causing human pathologies have been introduced in yeast mitoc...
A peculiar form of hepatocerebral mtDNA depletion syndrome is caused by mutations in the MPV17 gene,...