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. 2013 Aug;12(8):1142–1154. doi: 10.1128/EC.00123-13

Table 2.

Plasmids used in this study

Plasmid Description Source
B3782 3-kbp FLO11::lacZ in YEp355 53
p180 GCN4::lacZ reporter construct (uORFs 1 to 4) on a centromere vector (URA3) 59
p227 GCN4::lacZ reporter construct (without uORFs) on a centromere vector (URA3) 73
pAG25 NatMX4 cassette in pFA6 74
p426MET25 pRS426 containing MET25 promoter, CYC1 terminator 75
pFLO11-2/1 to pFLO11-15/14 440-bp sequence elements cloned into pLG669Z from bp −1 to −420, bp −180 to −620, and bp −380 to −1020 until bp −2580 to −2980 53
pLG669Z lacZ shuttle vector 76
pMCZ-Y UPRE-CYC1-lacZ reporter construct on multicopy vector (URA) 23
pME1092 2.8-kb GCN4 fragment in pRS314 57
pME1112 Integrative GCRE6::lacZ reporter construct 57
pME2212 pLG669Z without UASa 18
pME2213 Integrative FLO11::lacZ reporter construct Our collection
pME2901 GCN4prom-GCN4L267S-GCN4-term in pRS314 17
pME3378 GCN4prom-GCN4L253G-GCN4-term in pRS314 17
pME3498 MET25prom-HAC1 in p426MET25 This study
pRS314 TRP CEN Ampr ori 77
pRS426 URA3 2μm Ampr ori 77
a

UAS, upstream activation sequence.