The dihydroflavonol 4-reductase BoDFR1 drives anthocyanin accumulation in pink-leaved ornamental kale
Key message Overexpression and virus-induced gene silencing verified BoDFR1 conferred the anthocyanin accumulation in pink-leaved ornamental kale. Leaf color is an essential trait in the important horticultural biennial plant ornamental kale ( Brassica oleracea var. acephala ). The identity of the g...
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Veröffentlicht in: | Theoretical and applied genetics 2021, Vol.134 (1), p.159-169 |
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Overexpression and virus-induced gene silencing verified
BoDFR1
conferred the anthocyanin accumulation in pink-leaved ornamental kale.
Leaf color is an essential trait in the important horticultural biennial plant ornamental kale (
Brassica oleracea
var.
acephala
). The identity of the gene conferring this striking trait and its mode of inheritance are topics of debate. Based on an analysis of F
1
, F
2
, BC
1
P
1
, and BC
1
P
2
ornamental kale populations derived from a cross between a pink-leaved P28 and white-leaved D10 line, we determined that the pink leaf trait is controlled by a semi-dominant gene. We cloned two genes potentially involved in anthocyanin biosynthesis in ornamental kale:
Bo9g058630
and
Bo6g100940
. Based on their variation in sequence, we speculated that
Bo9g058630
, encoding the kale dihydroflavonol-4 reductase (BoDFR1) enzyme, plays a critical role in the development of the pink leaf trait. Indeed, an InDel marker specific for
BoDFR1
completely co-segregated with the pink leaf trait in our F
2
population. We then generated the
35Spro: DFR-GUS
overexpression vector, which we transformed into D10. Overexpression of
BoDFR1
indeed restored some anthocyanin accumulation in this white-leaved parental line. In addition, we targeted
BoDFR1
in P28 using virus-induced gene silencing. Again, silencing of
BoDFR1
resulted in a substantial decrease in anthocyanin accumulation. This work lays the foundation for further exploration of the mechanism underlying anthocyanin accumulation in pink-leaved ornamental kale. |
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ISSN: | 0040-5752 1432-2242 |
DOI: | 10.1007/s00122-020-03688-9 |