Notably, Wov can also induce trichome formation when expressed in potato (Additional file 4).
Consistent levels of expression were observed for each of the eleven PiAP genes during culture on different agar media and during infection on potato (Additional File 3).
We identified one case of de-exonization, one case of exon deletion, two cases of intronization, and one case of exonization in tomato and potato (Additional file 2).
Resistance genes are frequently clustered in the genome the result of both segmental and tandem duplications [ 36, 37] and this was also observed in tomato and potato (Additional file 1: Figure S1, B1 ring).
Here's one from the potato-chip file: I found a bruised banana that looked like Charlie Manson.
The expression of the β-ZIP transcription factor, as well as the expression of one unknown gene (cDNA STMGG84), was also regulated by photoperiod and phyB in potato (Additional files 2 and 3), suggesting they may regulate the tuberization process.
We have identified 18, 16, 18 and 16 NCX proteins from Brachypodium, foxtail millet, poplar and potato, respectively (Additional file 2: Table S1).
For the creation of a potato database index file, we used the NCBI FORMATDB utility.
Additionally, RB-related proteins, also affecting chromatin remodelling as previously discussed, are differentially-expressed in leafy spurge, poplar and potato (see Additional file 8).
Microsynteny between the two species is only interrupted by unilateral insertions of transposable elements in the potato sequences (Additional file 3).
