FIE

Information FIE

Description

Encodes a protein similar to the transcriptional regular of the animal Polycomb group and is involved in regulation of establishment of anterior-posterior polar axis in the endosperm and repression of flowering during vegetative phase. Mutation leads endosperm to develop in the absence of fertilization and flowers to form in seedlings and non-reproductive organs. Also exhibits maternal effect gametophytic lethal phenotype, which is suppressed by hypomethylation. Forms part of a large protein complex that can include VRN2 (VERNALIZATION 2), VIN3 (VERNALIZATION INSENSITIVE 3) and polycomb group proteins FERTILIZATION INDEPENDENT ENDOSPERM (FIE), CURLY LEAF (CLF) and SWINGER (SWN or EZA1). The complex has a role in establishing FLC (FLOWERING LOCUS C) repression during vernalization. In the ovule, the FIE transcript levels increase transiently just after fertilization.

Full Name

Transducin/WD40 repeat-like superfamily protein

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
2
Peaks
12,392
Non-redundant peaks
11,161

TF Classification

Familly
REM
Sub Familly
NA

Source AtTFDB

External IDs

JASPAR
Ensembl
AT3G20740
UniProt
Q9LT47
Genevisible
Q9LT47
RefSeq
NM_112965.1
Aliases
All peaks FIE
Download BED file
Non redundant peaks FIE
Download BED file
SEQUENCES FIE
Download FASTA file
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Datasets Table for FIE

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
FIE Ws Ws_whole-plant 30h-wt GEO Arabidopsis thaliana GSE95562 2,643
FIE Col Col_whole-plant 30h GEO Arabidopsis thaliana GSE84483 9,749
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.