Control plants were treated with 0.1% milk powder only. RNA isolation from infected and noninfected plants as well as from germinated spores was performed according to US Patent No. 5,973,137 (Heath, 1999). Three leaves of the same whorl were homogenized for 10 min in 14 mL lysis buffer (2% SDS, 68 mM sodium citrate, 132 mM citric acid, 10 mM EDTA, pH 3.5) using a glass potter. After the addition of 5 mL protein precipitation buffer (4 M sodium chloride, 17 mM sodium citrate, 33 mM citric acid, pH 3.5) and mixing, the solution

was kept on ice for 5 min. Cell debris was removed by centrifugation for 10 min at 4 °C and 20 000 g. The supernatant was transferred MK0683 to a new centrifuge tube and 14 mL isopropanol were added. After mixing, the solution was incubated at room temperature for 15 min. RNA was recovered by centrifugation at 20 000 g and 4 °C for 5 min. The supernatant was removed and the pellet

washed with 1.5 mL 75% ethanol. The supernatant was carefully removed after another centrifugation step Tofacitinib under identical conditions and the pellet dried for 10 min using a speedvac concentrator. RNA pellets were resuspended in water pretreated with diethylene pyrocarbonate (H2ODEPC) and stored at −80 °C. RNA isolations for each time point were done three times with independent sets of plants. Corresponding samples were pooled for further analysis. Urediospores (0.5 g) were washed with 200 mL 0.01% Tween20 for 20 min. Spores were collected by filtration, resuspended in 0.5 L Tween20 and vigorously stirred at room temperature in the dark for 4 h. Progress of germination was monitored microscopically. Germinated spores were collected by filtration and transferred to a mortar prechilled with liquid nitrogen.

Germlings were thoroughly ground for 20 min, continuously adding liquid nitrogen. Ground material was transferred to a centrifuge tube and after warming to 4 °C 14 mL of lysis buffer were added. Further steps were carried out as detailed above. Isolation of haustoria from infected V. faba leafs 8 days postinoculation (dpi) was performed as described by Hahn & Mendgen (1992) and RNA was prepared using peqGold RNAPure (Peqlab, Erlangen, Germany). All samples were subjected Neratinib in vivo to a Na-acetate/EtOH precipitation, resuspended in H2ODEPC, and quantified photometrically. Samples were adjusted to a concentration of 200 ng μL−1 and integrity of RNA was verified by gel electrophoresis. Primers for real-time PCR were designed based on sequences of genes determined in our laboratory. Genes CON1 and CON2 represent transcripts that were identified to be constitutively expressed in the initial expression analysis performed by Hahn & Mendgen (1997) [positions H2 (CON1) and L12 (CON2) in fig. 2 of Hahn & Mendgen (1997)]. TBB1 represents the β-tubulin gene of U. fabae, which also has been shown to be constitutively expressed (Wirsel et al., 2004).