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. Author manuscript; available in PMC: 2016 Nov 5.
Published in final edited form as: Mol Cell. 2015 Nov 5;60(3):500–508. doi: 10.1016/j.molcel.2015.09.027

Table 1.

Spectrum of GCR events

Relevant genotype CanR 5-FOAR mutation rate* Isolates analyzed Telomere addition Deletion/translocation Ch V left arm duplication (class I, class II)
WT 2.04 [± 0.72] × 10−10 (1.0) 121 9 1 1 (1, 0)
sae2Δ 1.11 [± 0.08] × 10−9 (5.4) 9 1 1 7 (4, 3)
mre11-H125N 2.70 [± 0.46] × 10−9 (13.2) 10 2 0 8 (6, 2)
rfa1-t33 4.20 [± 1.80 ] × 10−8 (205) 14 7 7 0 (0, 0)
rfa1-t33 sae2Δ 1.86 [± 1.10] × 10−6 (9079) 10 1 0 9 (9, 0)
rfa1-t33 mre11-H125N 2.75 [± 0.57] × 10−6 (13436) 10 3 0 7 (3, 4)
*

Rate of accumulating CanR 5-FOAR progeny. Numbers in brackets indicate standard deviation.

The number in parenthesis is the fold increase relative to wild type.

Class I: Duplication on Ch V and second homology dependent invasion

Class II: Duplication on Ch V only

1

One WT GCR clone contained a point mutation in the CAN1 gene and no discernable mutation at URA3. This clone was able to grow on 5-FOA containing and SC-URA media.

See also Figure S3.