FT-like paralogs are repressed by an SVP protein during the floral transition in Phalaenopsis orchid
Key message An SVP protein, PhSVP, bound to the CArG-boxes in the promoter regions of FT -like paralogs and repressed their expression, thus affecting the floral transition in Phalaenopsis orchid . Phalaenopsis is an important ornamental flower native to tropical rain forests. It usually reaches veg...
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Veröffentlicht in: | Plant cell reports 2022, Vol.41 (1), p.233-248 |
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An SVP protein, PhSVP, bound to the CArG-boxes in the promoter regions of
FT
-like paralogs and repressed their expression, thus affecting the floral transition in
Phalaenopsis
orchid
.
Phalaenopsis
is an important ornamental flower native to tropical rain forests. It usually reaches vegetative maturity after 4–5 leaves and, after a juvenile stage, forms a flower spike (inflorescence) from the axillary buds. The PEBP gene family encodes a phosphatidyl-ethanolamine-binding protein (PEBP) domain involved in regulating flowering and other aspects of plant development. Here, we identified eight PEBP family genes in
Phalaenopsis
and detected the expression patterns of seven of them in various organs. Among them,
PhFT1
(
Phalaenopsis
hybrid
FLOWERING LOCUS T1
),
PhFT3
,
PhFT5
, and
PhMFT
(
Phalaenopsis
hybrid
MOTHER OF FT AND TFL1
) promoted flowering in transgenic
Arabidopsis
, while
PhFT6
inhibited flowering. PhSVP (
Phalaenopsis
hybrid SHORT VEGETATIVE PHASE), an SVP protein that repressed flowering in
Arabidopsis
, bound to the CArG-boxes in the promoter regions of
PhFT3
,
PhFT6
, and
PhMFT
in a yeast one-hybrid assay. Additionally, dual-luciferase and transient expression assays showed that PhSVP significantly inhibits the expression of both
PhFT3
and
PhFT6
. Together, our work provides a comprehensive understanding of the
PhFT
-like genes that can promote or repress flowering, and it suggests strategies for regulating the floral transition in
Phalaenopsis
that exploit the evolutionary versatility of
PhFT
s to respond to various signals stimuli. |
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ISSN: | 0721-7714 1432-203X |
DOI: | 10.1007/s00299-021-02805-2 |