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Identification of Novel Human Damage Response Proteins Targeted through Yeast Orthology
by
Somoza, Luis A.
, Fry, Rebecca C.
, Wang, Emma
, Svensson, J. Peter
, Samson, Leona D.
in
4-Nitroquinoline-1-oxide - toxicity
/ Alkylating agents
/ Alkylating Agents - toxicity
/ Alkylation
/ Analysis
/ Apoptosis
/ Ataxia
/ Autophagy - physiology
/ Baking yeast
/ Bioengineering
/ Biology
/ Breast cancer
/ Cell cycle
/ Cell death
/ Cell Line
/ Cell lines
/ Cell survival
/ Cells (Biology)
/ Cellular biology
/ Chromatin
/ Chromatin Assembly and Disassembly - drug effects
/ Damage
/ Damage detection
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA Damage - drug effects
/ DNA repair
/ DNA Repair - genetics
/ Drosophila
/ Engineering
/ Environmental health
/ Gene expression
/ Genomes
/ Health sciences
/ Homology
/ Human behavior
/ Humans
/ Insects
/ Ionizing radiation
/ Medical research
/ Metabolism
/ Methyl Methanesulfonate - toxicity
/ Modulators
/ Mutagens - toxicity
/ Mutation
/ Orthology
/ Oxidation
/ Oxidizing agents
/ Phagocytosis
/ Phylogenetics
/ Physiological aspects
/ Protein interaction
/ Protein Interaction Maps
/ Protein metabolism
/ Protein turnover
/ Protein-protein interactions
/ Proteins
/ Quinolones - toxicity
/ Ribonucleic acid
/ RNA
/ RNA-mediated interference
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - genetics
/ Saccharomyces cerevisiae Proteins - genetics
/ Sequence Homology, Amino Acid
/ Survival
/ Telomeres
/ tert-Butylhydroperoxide - toxicity
/ Toxicity
/ Vesicular Transport Proteins - physiology
/ Yeast
2012
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Identification of Novel Human Damage Response Proteins Targeted through Yeast Orthology
by
Somoza, Luis A.
, Fry, Rebecca C.
, Wang, Emma
, Svensson, J. Peter
, Samson, Leona D.
in
4-Nitroquinoline-1-oxide - toxicity
/ Alkylating agents
/ Alkylating Agents - toxicity
/ Alkylation
/ Analysis
/ Apoptosis
/ Ataxia
/ Autophagy - physiology
/ Baking yeast
/ Bioengineering
/ Biology
/ Breast cancer
/ Cell cycle
/ Cell death
/ Cell Line
/ Cell lines
/ Cell survival
/ Cells (Biology)
/ Cellular biology
/ Chromatin
/ Chromatin Assembly and Disassembly - drug effects
/ Damage
/ Damage detection
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA Damage - drug effects
/ DNA repair
/ DNA Repair - genetics
/ Drosophila
/ Engineering
/ Environmental health
/ Gene expression
/ Genomes
/ Health sciences
/ Homology
/ Human behavior
/ Humans
/ Insects
/ Ionizing radiation
/ Medical research
/ Metabolism
/ Methyl Methanesulfonate - toxicity
/ Modulators
/ Mutagens - toxicity
/ Mutation
/ Orthology
/ Oxidation
/ Oxidizing agents
/ Phagocytosis
/ Phylogenetics
/ Physiological aspects
/ Protein interaction
/ Protein Interaction Maps
/ Protein metabolism
/ Protein turnover
/ Protein-protein interactions
/ Proteins
/ Quinolones - toxicity
/ Ribonucleic acid
/ RNA
/ RNA-mediated interference
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - genetics
/ Saccharomyces cerevisiae Proteins - genetics
/ Sequence Homology, Amino Acid
/ Survival
/ Telomeres
/ tert-Butylhydroperoxide - toxicity
/ Toxicity
/ Vesicular Transport Proteins - physiology
/ Yeast
2012
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Identification of Novel Human Damage Response Proteins Targeted through Yeast Orthology
by
Somoza, Luis A.
, Fry, Rebecca C.
, Wang, Emma
, Svensson, J. Peter
, Samson, Leona D.
in
4-Nitroquinoline-1-oxide - toxicity
/ Alkylating agents
/ Alkylating Agents - toxicity
/ Alkylation
/ Analysis
/ Apoptosis
/ Ataxia
/ Autophagy - physiology
/ Baking yeast
/ Bioengineering
/ Biology
/ Breast cancer
/ Cell cycle
/ Cell death
/ Cell Line
/ Cell lines
/ Cell survival
/ Cells (Biology)
/ Cellular biology
/ Chromatin
/ Chromatin Assembly and Disassembly - drug effects
/ Damage
/ Damage detection
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA Damage - drug effects
/ DNA repair
/ DNA Repair - genetics
/ Drosophila
/ Engineering
/ Environmental health
/ Gene expression
/ Genomes
/ Health sciences
/ Homology
/ Human behavior
/ Humans
/ Insects
/ Ionizing radiation
/ Medical research
/ Metabolism
/ Methyl Methanesulfonate - toxicity
/ Modulators
/ Mutagens - toxicity
/ Mutation
/ Orthology
/ Oxidation
/ Oxidizing agents
/ Phagocytosis
/ Phylogenetics
/ Physiological aspects
/ Protein interaction
/ Protein Interaction Maps
/ Protein metabolism
/ Protein turnover
/ Protein-protein interactions
/ Proteins
/ Quinolones - toxicity
/ Ribonucleic acid
/ RNA
/ RNA-mediated interference
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - genetics
/ Saccharomyces cerevisiae Proteins - genetics
/ Sequence Homology, Amino Acid
/ Survival
/ Telomeres
/ tert-Butylhydroperoxide - toxicity
/ Toxicity
/ Vesicular Transport Proteins - physiology
/ Yeast
2012
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Identification of Novel Human Damage Response Proteins Targeted through Yeast Orthology
Journal Article
Identification of Novel Human Damage Response Proteins Targeted through Yeast Orthology
2012
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Overview
Studies in Saccharomyces cerevisiae show that many proteins influence cellular survival upon exposure to DNA damaging agents. We hypothesized that human orthologs of these S. cerevisiae proteins would also be required for cellular survival after treatment with DNA damaging agents. For this purpose, human homologs of S. cerevisiae proteins were identified and mapped onto the human protein-protein interaction network. The resulting human network was highly modular and a series of selection rules were implemented to identify 45 candidates for human toxicity-modulating proteins. The corresponding transcripts were targeted by RNA interference in human cells. The cell lines with depleted target expression were challenged with three DNA damaging agents: the alkylating agents MMS and 4-NQO, and the oxidizing agent t-BuOOH. A comparison of the survival revealed that the majority (74%) of proteins conferred either sensitivity or resistance. The identified human toxicity-modulating proteins represent a variety of biological functions: autophagy, chromatin modifications, RNA and protein metabolism, and telomere maintenance. Further studies revealed that MMS-induced autophagy increase the survival of cells treated with DNA damaging agents. In summary, we show that damage recovery proteins in humans can be identified through homology to S. cerevisiae and that many of the same pathways are represented among the toxicity modulators.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
4-Nitroquinoline-1-oxide - toxicity
/ Alkylating Agents - toxicity
/ Analysis
/ Ataxia
/ Biology
/ Chromatin Assembly and Disassembly - drug effects
/ Damage
/ DNA
/ Genomes
/ Homology
/ Humans
/ Insects
/ Methyl Methanesulfonate - toxicity
/ Mutation
/ Protein-protein interactions
/ Proteins
/ RNA
/ Saccharomyces cerevisiae - genetics
/ Saccharomyces cerevisiae Proteins - genetics
/ Sequence Homology, Amino Acid
/ Survival
/ tert-Butylhydroperoxide - toxicity
/ Toxicity
/ Vesicular Transport Proteins - physiology
/ Yeast
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