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Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes
by
Brunette, Gregory J.
, Jamalruddin, Mohd A.
, Clark, Nathan L.
, Baldock, Robert A.
, Bernstein, Kara A.
in
Anemia
/ Animals
/ Apoptosis
/ Apoptosis Regulatory Proteins - genetics
/ Apoptosis Regulatory Proteins - metabolism
/ Biological evolution
/ Biological Sciences
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Coevolution
/ Computer applications
/ Deoxyribonucleic acid
/ DNA
/ DNA Breaks, Double-Stranded
/ DNA damage
/ DNA repair
/ DNA Repair - genetics
/ Double-strand break repair
/ Evolution, Molecular
/ Evolutionary genetics
/ Fanconi syndrome
/ Genes
/ Genetic screening
/ Genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Genomic Instability - genetics
/ Homologous recombination
/ Homologous Recombination - genetics
/ Homology
/ Humans
/ Kinases
/ Mammals
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Repair
/ Screening
2019
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Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes
by
Brunette, Gregory J.
, Jamalruddin, Mohd A.
, Clark, Nathan L.
, Baldock, Robert A.
, Bernstein, Kara A.
in
Anemia
/ Animals
/ Apoptosis
/ Apoptosis Regulatory Proteins - genetics
/ Apoptosis Regulatory Proteins - metabolism
/ Biological evolution
/ Biological Sciences
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Coevolution
/ Computer applications
/ Deoxyribonucleic acid
/ DNA
/ DNA Breaks, Double-Stranded
/ DNA damage
/ DNA repair
/ DNA Repair - genetics
/ Double-strand break repair
/ Evolution, Molecular
/ Evolutionary genetics
/ Fanconi syndrome
/ Genes
/ Genetic screening
/ Genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Genomic Instability - genetics
/ Homologous recombination
/ Homologous Recombination - genetics
/ Homology
/ Humans
/ Kinases
/ Mammals
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Repair
/ Screening
2019
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Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes
by
Brunette, Gregory J.
, Jamalruddin, Mohd A.
, Clark, Nathan L.
, Baldock, Robert A.
, Bernstein, Kara A.
in
Anemia
/ Animals
/ Apoptosis
/ Apoptosis Regulatory Proteins - genetics
/ Apoptosis Regulatory Proteins - metabolism
/ Biological evolution
/ Biological Sciences
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ Coevolution
/ Computer applications
/ Deoxyribonucleic acid
/ DNA
/ DNA Breaks, Double-Stranded
/ DNA damage
/ DNA repair
/ DNA Repair - genetics
/ Double-strand break repair
/ Evolution, Molecular
/ Evolutionary genetics
/ Fanconi syndrome
/ Genes
/ Genetic screening
/ Genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Genomic Instability - genetics
/ Homologous recombination
/ Homologous Recombination - genetics
/ Homology
/ Humans
/ Kinases
/ Mammals
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Repair
/ Screening
2019
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Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes
Journal Article
Evolution-based screening enables genome-wide prioritization and discovery of DNA repair genes
2019
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Overview
DNA repair is critical for genome stability and is maintained through conserved pathways. Traditional genome-wide mammalian screens are both expensive and laborious. However, computational approaches circumvent these limitations and are a powerful tool to identify new DNA repair factors. By analyzing the evolutionary relationships between genes in the major DNA repair pathways, we uncovered functional relationships between individual genes and identified partners. Here we ranked 17,487 mammalian genes for coevolution with 6 distinct DNA repair pathways. Direct comparison to genetic screens for homologous recombination or Fanconi anemia factors indicates that our evolution-based screen is comparable, if not superior, to traditional screening approaches. Demonstrating the utility of our strategy, we identify a role for the DNA damage-induced apoptosis suppressor (DDIAS) gene in double-strand break repair based on its coevolution with homologous recombination. DDIAS knockdown results in DNA double-strand breaks, indicated by ATM kinase activation and 53BP1 foci induction. Additionally, DDIAS-depleted cells are deficient for homologous recombination. Our results reveal that evolutionary analysis is a powerful tool to uncover novel factors and functional relationships in DNA repair.
Publisher
National Academy of Sciences
Subject
/ Animals
/ Apoptosis Regulatory Proteins - genetics
/ Apoptosis Regulatory Proteins - metabolism
/ Cell Cycle Proteins - genetics
/ Cell Cycle Proteins - metabolism
/ DNA
/ Genes
/ Genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Genomic Instability - genetics
/ Homologous Recombination - genetics
/ Homology
/ Humans
/ Kinases
/ Mammals
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Repair
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