AP2
|
AINTEGUMENTA (ANT)
|
ANT initiates floral organ development [87]. It was shown to play a critical role in regulating the ovule and female gametophyte development [88].
|
C2H2
|
RESPONSIVE TO HIGH LIGHT 41 (Zat2)
|
Zat12 was originally isolated as a light stress-response cDNA [89]; then, it was suggested to be able to regulate transcripts involved in the response to high-light, cold and oxidative stress [90].
|
MADS box/MIKC
|
AGL19
|
AGL19 controls (promotes) flowering downstream of a cold-perception pathway and acts independently of FT and SOC1 [42].
|
MADS box/MIKC
|
FLOWERING LOCUS C (FLC)
|
FLC acts as an inhibitor of flowering [45].
|
MADS box/MIKC
|
MAF2 (AGL31)
|
MAF2 (AGL31), a paralog of FLC, is another flowering repressor that acts in non-inductive photoperiods [46, 47].
|
MADS box/MIKC
|
AGL69 (MAF5)
|
MAF5 is normally repressed. Overexpression of MAF5 under a non-inductive day length causes late-flowering [48].
|
MADS box/MIKC
|
AGL68 (MAF4)
|
MAF4 represses the transition to flowering [49, 50].
|
MADS box/MIKC
|
FLM (AGL27, MAF1)
|
FLM acts as a flowering inhibitor [51].
|
MADS box/MIKC
|
AGL6
|
AGL6 was suggested to be able to act as a flowering repressor or activator, depending on the context [43].
|
MADS box/MIKC
|
AGL14 (XAANTAL2, XAL2)
|
XAL2 is essential for flowering induction. XAL2 promotes flowering in response to different signals and is important for the maintenance and differentiating of flowering meristems [44].
|
MADS box/MIKC
|
AGAMOUS-like 15 (AGL15)
|
AGL15 and AGL18 are floral transition repressors. The agl15 agl18 mutants were characterized by a partial suppression of the photoperiod pathway [52].
|
MADS box/MIKC
|
AGAMOUS-like 18 (AGL18)
|
Lyase Aromatic
|
Phenylalanine Ammonia-Lyase (PAL1)
|
PAL1 is a light response element. These motifs are conserved at similar positions in several elicitor or light-responsive genes from different species [91].
|
–
|
RBCSGBOXPS
|
RBCSGBOXPS binding site, identified in Parsley, is involved in light responsiveness [92].
|
–
|
REBETALGLHCB21
|
REBETALGLHCB21, first found in the Lemna dibba Lhcb genes, is necessary for phytochrome regulation. These elements are likely to function by repressing the promoter activity in the dark [93].
|
–
|
SORLIP5AT
|
SORLIP5AT are PhyA-induced motifs that are overrepresented in light-induced genes. These elements, which predominate in the early responsive promoters, are more likely to have the fewest steps in the signal transduction cascade to gene expression [66].
|
–
|
MNF1ZMPPC1
|
MNF1ZMPPC1 is involved in the light-dependent transcriptional control of gene expression [94].
|