Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Jordi Moreno-Romero
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Yichun Qiu
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Joram van Boven
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Juan Santos-González
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences, Uppsala, Sweden; Linnean Centre for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden
MADS-box transcription factors (TFs) are ubiquitous in eukaryotic organisms and play major roles during plant development. Nevertheless, their function in seed development remains largely unknown. Here, we show that the imprinted Arabidopsis thaliana MADS-box TF PHERES1 (PHE1) is a master regulator of paternally expressed imprinted genes, as well as of non-imprinted key regulators of endosperm development. PHE1 binding sites show distinct epigenetic modifications on maternal and paternal alleles, correlating with parental-specific transcriptional activity. Importantly, we show that the CArG-box-like DNA-binding motifs that are bound by PHE1 have been distributed by RC/Helitron transposable elements. Our data provide an example of the molecular domestication of these elements which, by distributing PHE1 binding sites throughout the genome, have facilitated the recruitment of crucial endosperm regulators into a single transcriptional network.