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. 2001 Oct;183(19):5589–5598. doi: 10.1128/JB.183.19.5589-5598.2001

TABLE 4.

Interaction of HrpR and HrpS detected by yeast two-hybrid analysis

L40 transformant plasmid(s) LexA′-BD fusion GAL4′-AD fusion β-Galactosidase activitya
pDWR3BTM HrpR Absent <1
pDWS4BTM HrpS Absent <1
pBTM-lamin, pDWR3GAD Lamin HrpR <1
pBTM-lamin, pDWS4GAD Lamin HrpS <1
pDWR3BTM, pGAD424 HrpR None <1
pDWS4BTM, pGAD424 HrpS None 1.4 ± 0.6
pDWR3BTM, pDWR3GAD HrpR HrpR <1
pDWS4BTM, pDWS4GAD HrpS HrpS 3 ± 0.3
pDWR3BTM, pDWS4GAD HrpR HrpS 29 ± 10
pDWS4BTM, pDWR3GAD HrpS HrpR 28 ± 10
pDWS4BTM, pTSR4GAD HrpS HrpRΔN 26 ± 3
pDWS4BTM, pTSR5GAD HrpS HrpRΔC 1.4 ± 0.5
pDWS4BTM, pTSR6GAD HrpS HrpRΔNΔC 1.0 ± 0.2
a

The indicated S. cerevisiae L40 transformants were grown overnight at 25°C in defined medium lacking Leu and/or Trp (as required to maintain selection for plasmids) to an OD600 of 1.0. Cells were harvested and lysed by three freezing cycles in liquid N2, and β-galactosidase activity was determined as indicated in Materials and Methods.