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. 2013 Apr;193(4):1117–1133. doi: 10.1534/genetics.113.149849

Table 2. Tabulation of phenotypes for tel1-Δ interactions identified in the MMS screen.

Strain MMS interaction IR interaction GCR Short telomere CDC13-EST2 rescue Description
Class 1 rad24-Δtel1-Δ ++ + ++ ++ +/− 9-1-1 complex
rad17-Δtel1-Δ ++ + ++ ++ +/− 9-1-1 complex
ddc1-Δtel1-Δ ++ + ++ ++ +/− 9-1-1 complex
Class 2 nup60-Δtel1-Δ + + + Nucleoporin
rad27-Δtel1-Δ + + + Flap endonuclease
sap30-Δtel1-Δ + + Deacetylase
pop2-Δtel1-Δ + + Deadenylase
ccr4-Δtel1-Δ + + Deadenylase
hda3-Δtel1-Δ + + deacetylase
yku80-Δtel1-Δ + + NHEJ
nup133-Δtel1-Δ + + Nucleoporin
Class 3 lsm7-Δtel1-Δ + mRNA decap
rad26-Δtel1-Δ + TCR

For each of the tel1-Δ xxx-Δ genetic interactions identified in the MMS screen a “+” indicates whether a double mutant exhibited a positive result in each of the assays tested (e.g., increased GCR frequency, shorter telomere, etc.); a “++” indicates a more severe phenotype; and a “+/−” indicates partial suppression. TCR, transcription-coupled repair.