Table 1.
Leaf | Root | |||
---|---|---|---|---|
(A) Diploids | ||||
A. halleri | A. lyrata | A. halleri | A. lyrata | |
Upregulated | 889 | 355 | 232 | 5,095 |
Downregulated | 1,103 | 187 | 614 | 5,458 |
Total | 1,992 | 542 | 846 | 10,553 |
(B) A. kamchatica | ||||
MUR (Murodo, JP) | H-origin | L-origin | H-origin | L-origin |
Upregulated | 313 | 297 | 1,030 | 1,006 |
Downregulated | 384 | 358 | 1,345 | 1,332 |
Total | 697 | 655 | 2,375 | 2,338 |
(C) A. kamchatica | ||||
PAK (Potter, AK) | H-origin | L-origin | H-origin | L-origin |
Upregulated | 220 | 226 | 1,527 | 1,441 |
Downregulated | 696 | 661 | 1,480 | 1,353 |
Total | 916 | 887 | 3,007 | 2,794 |
Note.—(A) Diploids A. halleri subsp. gemmifera genotype (Tada mine) and A. lyrata subsp. petraea genotype w1178. Allopolyploid genes significantly up- or down-regulated in A. halleri-derived (H-origin) and A. lyrata-derived (L-origin) homeologs for A. kamchatica genotypes (B) MUR (Murodo, Japan) and (C) PAK (Potter, Alaska). The significance threshold is set to a FDR-adjusted P < 0.05 and expression between control to zinc-treated conditions must add up to RPKM ≥ 0.2.