Genome-Wide Dynamic Evaluation of the UV-Induced DNA Damage Response.
Erica SilvaManuel MichacaBrenton MunsonGordon J BeanPhilipp A JaegerKatherine LiconElizabeth A WinzelerTrey IdekerPublished in: G3 (Bethesda, Md.) (2020)
Genetic screens in Saccharomyces cerevisiae have allowed for the identification of many genes as sensors or effectors of DNA damage, typically by comparing the fitness of genetic mutants in the presence or absence of DNA-damaging treatments. However, these static screens overlook the dynamic nature of DNA damage response pathways, missing time-dependent or transient effects. Here, we examine gene dependencies in the dynamic response to ultraviolet radiation-induced DNA damage by integrating ultra-high-density arrays of 6144 diploid gene deletion mutants with high-frequency time-lapse imaging. We identify 494 ultraviolet radiation response genes which, in addition to recovering molecular pathways and protein complexes previously annotated to DNA damage repair, include components of the CCR4-NOT complex, tRNA wobble modification, autophagy, and, most unexpectedly, 153 nuclear-encoded mitochondrial genes. Notably, mitochondria-deficient strains present time-dependent insensitivity to ultraviolet radiation, posing impaired mitochondrial function as a protective factor in the ultraviolet radiation response.
Keyphrases
- genome wide
- dna damage
- dna damage response
- dna repair
- radiation induced
- oxidative stress
- high density
- high frequency
- dna methylation
- copy number
- saccharomyces cerevisiae
- diabetic rats
- transcranial magnetic stimulation
- radiation therapy
- high resolution
- cell death
- escherichia coli
- gene expression
- single molecule
- physical activity
- bioinformatics analysis
- dendritic cells
- body composition
- wild type
- genome wide identification
- circulating tumor
- transcription factor
- small molecule
- protein protein
- low cost
- drug induced
- single cell
- binding protein