Mitochondrial genetics X: Effects of UV irradiation on transmission and recombination of mitochondrial genes in Saccharomyces cerevisiae

1975 ◽  
Vol 137 (1) ◽  
pp. 29-72 ◽  
Author(s):  
B. Dujon ◽  
A. Kruszewska ◽  
P. P. Slonimski ◽  
M. Bolotin-Fukuhara ◽  
D. Coen ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Uv Irradiation ◽  
Mitochondrial Genes ◽  
Mitochondrial Genetics

scholarly journals A Synthetic Interaction between CDC20 and RAD4 in Saccharomyces cerevisiae upon UV Irradiation

2014 ◽  
Vol 2014 ◽  
pp. 1-8
Author(s):  
Bernadette Connors ◽  
Lauren Rochelle ◽  
Asela Roberts ◽  
Graham Howard
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Nucleotide Excision Repair ◽  
Uv Irradiation ◽  
Double Mutant ◽  
Excision Repair ◽  
Strand Break ◽  
Anaphase Promoting Complex ◽  
End Joining ◽  
Ubiquitin Ligase Complex ◽  
Nucleotide Excision

Regulation of DNA repair can be achieved through ubiquitin-mediated degradation of transiently induced proteins. In Saccharomyces cerevisiae, Rad4 is involved in damage recognition during nucleotide excision repair (NER) and, in conjunction with Rad23, recruits other proteins to the site of damage. We identified a synthetic interaction upon UV exposure between Rad4 and Cdc20, a protein that modulates the activity of the anaphase promoting complex (APC/C), a multisubunit E3 ubiquitin ligase complex. The moderately UV sensitive Δrad4 strain became highly sensitive when cdc20-1 was present, and was rescued by overexpression of CDC20. The double mutant is also deficient in elicting RNR3-lacZ transcription upon exposure to UV irradiation or 4-NQO compared with the Δrad4 single mutant. We demonstrate that the Δrad4/cdc20-1 double mutant is defective in double strand break repair by way of a plasmid end-joining assay, indicating that Rad4 acts to ensure that damaged DNA is repaired via a Cdc20-mediated mechanism. This study is the first to present evidence that Cdc20 may play a role in the degradation of proteins involved in nucleotide excision repair.

scholarly journals Transcriptomic analysis and driver mutant prioritization for differentially expressed genes from a Saccharomyces cerevisiae strain with high glucose tolerance generated by UV irradiation

RSC Advances ◽  
2017 ◽  
Vol 7 (62) ◽  
pp. 38784-38797 ◽  
Author(s):  
Ying Chen ◽  
Zhilong Lu ◽  
Dong Chen ◽  
Yutuo Wei ◽  
Xiaoling Chen ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Glucose Tolerance ◽  
Differentially Expressed Genes ◽  
Uv Irradiation ◽  
High Glucose ◽  
Mutant Phenotype ◽  
Differentially Expressed ◽  
Driver Mutations ◽  
High Sugar ◽  
Sugar Tolerance

Driver mutations of a Saccharomyces cerevisiae mutant phenotype strain with high sugar tolerance were sought by the PheNetic network.

scholarly journals The essential DNA polymerases delta and epsilon are involved in repair of UV-damaged DNA in the yeast Saccharomyces cerevisiae.

1999 ◽  
Vol 46 (2) ◽  
pp. 289-298 ◽  
Author(s):  
A Hałas ◽  
Z Policińska ◽  
H Baranowska ◽  
W J Jachymczyk
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Dna Repair ◽  
Uv Irradiation ◽  
Dna Polymerases ◽  
Relative Molecular Mass ◽  
Yeast Saccharomyces Cerevisiae ◽  
Strand Breaks ◽  
Single Strand Breaks ◽  
Mutant Strains ◽  
Cellular Dna

We have studied the ability of yeast DNA polymerases to carry out repair of lesions caused by UV irradiation in Saccharomyces cerevisiae. By the analysis of postirradiation relative molecular mass changes in cellular DNA of different DNA polymerases mutant strains, it was established that mutations in DNA polymerases delta and epsilon showed accumulation of single-strand breaks indicating defective repair. Mutations in other DNA polymerase genes exhibited no defects in DNA repair. Thus, the data obtained suggest that DNA polymerases delta and epsilon are both necessary for DNA replication and for repair of lesions caused by UV irradiation. The results are discussed in the light of current concepts concerning the specificity of DNA polymerases in DNA repair.

Transcriptional analysis of the Saccharomyces cerevisiae mitochondrial var1 gene: anomalous hybridization of RNA from AT-rich regions

1983 ◽  
Vol 3 (9) ◽  
pp. 1615-1624
Author(s):  
H P Zassenhaus ◽  
F Farrelly ◽  
M E Hudspeth ◽  
L I Grossman ◽  
R A Butow
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Mitochondrial Genes ◽  
Transcriptional Analysis ◽  
Asymmetric Distribution ◽  
Direct Function ◽  
Important Conclusion ◽  
The Family ◽  
Var1 Gene ◽  
Flanking Sequences ◽  
Transcription Map

A family of mitochondrial RNAs hybridizes specifically to the var1 region on Saccharomyces cerevisiae mitochondrial DNA (Farrelly et al., J. Biol. Chem. 257:6581-6587, 1982). We constructed a fine-structure transcription map of this region by hybridizing DNA probes containing different portions of the var1 region and some flanking sequences to mitochondrial RNAs isolated from var1-containing petites. We also report the nucleotide sequence of more than 1.2 kilobases of DNA flanking the var1 gene. Our primary findings are: (i) The family of RNAs we detect with homology to var1 DNA is colinear with the var1 gene. Their direction of transcription is olil to cap, as it is for most other mitochondrial genes. (ii) Extensive hybridization anomalies are present, most likely due to the high A-T (A-U) content of the hybridizing species and to the asymmetric distribution of their G-C residues. An important conclusion is that failure to detect transcripts from A-T-rich regions of the yeast mitochondrial genome by standard blot transfer hybridizations cannot be interpreted to mean that such sequences, which are commonly supposed to be spacer DNA, are noncoding or lack direct function in the expression of mitochondrial genes.

scholarly journals Transcriptional analysis of the Saccharomyces cerevisiae mitochondrial var1 gene: anomalous hybridization of RNA from AT-rich regions.

1983 ◽  
Vol 3 (9) ◽  
pp. 1615-1624 ◽  
Author(s):  
H P Zassenhaus ◽  
F Farrelly ◽  
M E Hudspeth ◽  
L I Grossman ◽  
R A Butow
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Mitochondrial Genes ◽  
Transcriptional Analysis ◽  
Asymmetric Distribution ◽  
Direct Function ◽  
Important Conclusion ◽  
The Family ◽  
Var1 Gene ◽  
Flanking Sequences ◽  
Transcription Map

A family of mitochondrial RNAs hybridizes specifically to the var1 region on Saccharomyces cerevisiae mitochondrial DNA (Farrelly et al., J. Biol. Chem. 257:6581-6587, 1982). We constructed a fine-structure transcription map of this region by hybridizing DNA probes containing different portions of the var1 region and some flanking sequences to mitochondrial RNAs isolated from var1-containing petites. We also report the nucleotide sequence of more than 1.2 kilobases of DNA flanking the var1 gene. Our primary findings are: (i) The family of RNAs we detect with homology to var1 DNA is colinear with the var1 gene. Their direction of transcription is olil to cap, as it is for most other mitochondrial genes. (ii) Extensive hybridization anomalies are present, most likely due to the high A-T (A-U) content of the hybridizing species and to the asymmetric distribution of their G-C residues. An important conclusion is that failure to detect transcripts from A-T-rich regions of the yeast mitochondrial genome by standard blot transfer hybridizations cannot be interpreted to mean that such sequences, which are commonly supposed to be spacer DNA, are noncoding or lack direct function in the expression of mitochondrial genes.

scholarly journals MITOCHONDRIAL GENETICS. VI THE PETITE MUTATION IN SACCHAROMYCES CEREVISIAE: INTERRELATIONS BETWEEN THE LOSS OF THE ρ+ FACTOR AND THE LOSS OF THE DRUG RESISTANCE MITOCHONDRIAL GENETIC MARKERS

Genetics ◽  
1974 ◽  
Vol 76 (2) ◽  
pp. 195-219
Author(s):  
J Deutsch ◽  
B Dujon ◽  
P Netter ◽  
E Petrochilo ◽  
P P Slonimski ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Drug Resistance ◽  
Mitochondrial Genome ◽  
Genetic Marker ◽  
Genetic Markers ◽  
The Other ◽  
Mitochondrial Genetics ◽  
Petite Mutation ◽  
Target Theory

ABSTRACT The survival of the ρ+ factor and of DrugR mitochondrial genetic markers after exposure to ethidium bromide has been studied. A technique allowing the determination of DrugR genetic markers among a great number of both grande and petite colonies has been developed. The results have been analyzed by the target theory. The survival of the ρ+ factor is always less than the survival of any DrugR genetic marker. The survivals of CR and ER are similar to each other, while that of OR is greater than that of the other two DrugR markers. All possible combinations of DrugR markers have been found among the ρ- petite cells induced, while the only type found among the grande colonies is the preexisting one. The loss of the CR and ER genetic markers was found to be the most frequently concomitant, while the correlation between the loss of the OR marker and the other two DrugR markers is less strong. Similar results have been obtained after U.V. irradiation. Interpretations concerning the structure of the yeast mitochondrial genome are given and hypotheses on the mechanism of petite mutation discussed.

Differential repair of UV damage in rad mutants of Saccharomyces cerevisiae: a possible function of G2 arrest upon UV irradiation

1990 ◽  
Vol 10 (9) ◽  
pp. 4678-4684
Author(s):  
C Terleth ◽  
P Schenk ◽  
R Poot ◽  
J Brouwer ◽  
P van de Putte
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Uv Irradiation ◽  
Uv Damage ◽  
G2 Arrest ◽  
Rad Mutants

After UV irradiation, the transcriptionally active MAT alpha locus in Saccharomyces cerevisiae is preferentially repaired compared with the inactive HML alpha locus. The effect of rad mutations from three different epistasis groups on differential repair was investigated. Three mutants, rad9, rad16, and rad24, were impaired in the removal of UV dimers from the inactive HML alpha locus, whereas they had generally normal repair of the active MAT alpha locus. Since RAD9 is necessary for G2 arrest after UV irradiation, we propose that the G2 stage plays a role in making the dimers accessible for repair, at least in the repressed HML alpha locus.

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