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. 2012 Oct 18;8(10):e1002976. doi: 10.1371/journal.pgen.1002976

Table 1. Rates of ura4 loss (including genomic deletion, translocation, and mutation events), calculated using the method of the median.

strainsa Rate of ura4 lossb Fold induction by Rtf1 expression (−/+ thiamine)c Fold induction by the RFB (relative to the t-ura4-ori construct)
+ thiamine (Rtf1 repressed) − thiamine (Rtf1 expressed)
t-ura4-ori 4.6±1 4.3±1.8 0.9
t-ura4<ori 4.1±0.9 13.9±2.8 3.4 (p = 0.002) 3.2
t-ura4<ori RTS1-d 4.9±1.4 11.4±4.1 2.3 (p = 0.03) 2.6
t<ura4-ori 3.9±1.3 4.8±2.5 1.2 1.1
t>ura4<ori 5.8±2.1 97.4±51.5 16.8 (p = 0.004) 22.6
t>ura4<ori RTS1-d 4.9±2.2 19.5±3.3 4 (p = 0.006) 4.5
t>ura4-ori 3.2±1.7 3.6±1.8 1.1 0.8
t<ura4>ori 6.6±1.7 50.3±14.2 7.6 (p = 0.014) 11.7
a

the following nomenclature is used: “t” and “ori” refer to the telomere and the replication origin 3006/7, respectively; “<“ and ”>” indicate the RTS1-RFB and its polarity (< blocks replication forks moving from the ori3006/7 towards the telomere, and > blocks replication forks moving from the telomere towards the origin 3006/7).

b

event/cell/division ×10−8 ± standard error. Values are means of at least 3 independent rates.

c

statistical significance was determined using the nonparametric Mann-Whitney U test.