Gene Details:

  • Gene ID: EcC053935.30
  • Gene Family: FAR1 Family
  • Description: FAR1 Family protein
  • Species: Eucalyptus camaldulensis
  • Source: FAR1 family gene from PlantTFDB

Protein Features:

Gene Ontology:

  • GO:0015074  — Biological Process — DNA integration
  • GO:0055114  — Biological Process — oxidation-reduction process
  • GO:0005737  — Cellular Component — cytoplasm
  • GO:0003676  — Molecular Function — nucleic acid binding
  • GO:0005506  — Molecular Function — iron ion binding
  • GO:0016705  — Molecular Function — oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
  • GO:0020037  — Molecular Function — heme binding

Family Introduction:

  • We show that Arabidopsis FHY3 and FAR1, which encode two proteins related to Mutator-like transposases, act together to modulate phyA signaling by directly activating the transcription of FHY1 and FHL, whose products are essential for light-induced phyA nuclear accumulation and subsequent light responses. FHY3 and FAR1 have separable DNA binding and transcriptional activation domains that are highly conserved in Mutator-like transposases. Further, expression of FHY3 and FAR1 is negatively regulated by phyA signaling. We propose that FHY3 and FAR1 represent transcription factors that have been co-opted from an ancient Mutator-like transposase(s) to modulate phyA-signaling homeostasis in higher plants.
  • We next used a yeast one-hybrid assay to delineate the DNA sequences to which FHY3 and FAR1 bind. GAD-FHY3 or GAD-FAR1 fusion proteins (GAD, GAL4 transcriptional activation domain), but not GAD alone, activated the LacZ reporter genes driven by the FHY1 and FHL promoters. Deletion analysis narrowed down the FHY3/FAR1 binding site to a 39-bp promoter subfragment located on the ‘a’ fragment for both FHY1 and FHL. Notably, these subfragments share a stretch of consensus sequence, 5’-TTCACGCGCC-3’. Mutating the core sequence ‘CACGCGC’ of this motif (m2 and m3 for FHY1, m5 for FHL) abolished the reporter gene activation by both GAD-FHY3 and GAD-FAR1. Mutating the flanking sequences (m1 and m4) did not obviously affect the reporter gene activation by GAD-FAR1, but clearly reduced activation by GAD-FHY3. Thus, ‘CACGCGC’ likely defines a cis-element that confers specific binding for FHY3 and FAR1 and is named FBS for FHY3-FAR1 binding site.

Literature:

Sequences:

CDS Sequence:
  • >EcC053935.30|Eucalyptus_camaldulensis|FAR1|EcC053935.30
    ATGGAGTTTAATTCTTATGATAAGGCTTATGCATTTTATGACAATTGTGCTAAAGAAGCGGGATTTGAAATTAGAGTGAACTCTCATAAAAGGAAAGGCAGCAAGGAAAAATGTGGTGCAGTACTTTGTTGCATTTGTCAAGGGTACAAGATCGAAAAAGAGTTGGTTAAGTCAAGATCGAGAAAAAGCTATGGTTGTCTAACAATGGTTAGAATACATCTAGTTGAGCCTCAAAAGTGGAAAATAGCAAAAGTTGTTATAGAAGGAAGATATGAGAACTTAAATTTTGAAGGAAAAGATGTTAGAAATCATGTTGAGAGATACAAAAGGATGAAATTGCAAGAAGGAGATGGGCAAGTACTTTTCAATTATTTTTCAACCATGTTATTGAAAATTTCCATTTTTTATTATGTGCTTGATTTGGATAATGAGCAGAGATTGTATAATATCTTCTGGGTAGAAGCACAATCAAGAGACGCATATACATATTTTGGAGATGTAGTCACATTTGATACAACTTATTTCAAAGCAATTTTGGAGACATAA
Protein Sequence:
  • >EcC053935.30|Eucalyptus_camaldulensis|FAR1|EcC053935.30
    MEFNSYDKAYAFYDNCAKEAGFEIRVNSHKRKGSKEKCGAVLCCICQGYKIEKELVKSRSRKSYGCLTMVRIHLVEPQKWKIAKVVIEGRYENLNFEGKDVRNHVERYKRMKLQEGDGQVLFNYFSTMLLKISIFYYVLDLDNEQRLYNIFWVEAQSRDAYTYFGDVVTFDTTYFKAILET