Table 2.
Gene | Accession number | Wild‐type/Δsnt2 expression ratio* | Description |
---|---|---|---|
idi4 † | FOXG_04081 | 24.5 ± 2.25+ | Induced during incompatibility |
cpc1 | FOXG_05954 | 2.12 ± 0.09 | Cross‐pathway control |
pdc † | BAE98181.1 | 20.78 ± 7.04+ | Pyruvate decarboxylase |
fnr1 | DQ387858 | 1.2 ± 0.15 | Global nitrogen regulator |
nit4 | FOXG_06396 | 0.95 ± 0.08 | Pathway‐specific nitrogen regulator |
glnA | FOXG_05182 | 4.02 ± 0.50 | Glutamine synthetase |
mfs1 † | FOXG_09760 | 1.60 ± 0.86 | Transporter of the major facilitator family |
rbs1 † | FOXG_14252 | 0.15 ± 0.03‐ | Unknown functions |
eEF1G † | FOXG_01492 | 2.72 ± 1.21 | Translation elongation factor |
cDNA was synthesized from 1 µg of total RNA. All samples were analysed in triplicate. Averaged crossing point values were normalized to the endogenous control gene β‐tubulin. Gene expression level and comparative analyses (*) of two biological and four technical repeats were evaluated using the REST© program (Pfaffl et al., 2002). Accession numbers were according to http://www.broad.mit.edu and National Center for Biotechnology Information (NCBI) databases. Statistically significant changes are marked by += up‐regulated and −= down‐regulated.
Identified by suppressive subtraction hybridization (SSH) screen.