These results reveal novel cis-element/ trans-factor interactions functionally associated with iron homeostasis.įIGURE 2 Determination of precise IDEF2-binding sequences by EMSA and CASTing. IDEF2 bound to OsYSL2 promoter region containing the binding core site, suggesting direct regulation of OsYSL2 expression. Many genes with repressed expression in IDEF2 RNAi rice possessed the IDEF2-binding core sites in their promoters, and the flanking sequences were also highly homologous to IDE2. Several genes up-regulated by iron deficiency, including the Fe(II)-nicotianamine transporter gene OsYSL2, were less induced by iron deficiency in the RNAi rice of IDEF2, suggesting that IDEF2 is involved in the regulation of these genes. Repression of the function of IDEF2 by the RNA interference (RNAi) technique and chimeric repressor gene- silencing technology (CRES-T) caused aberrant iron homeostasis in rice. IDEF2 transcripts are constitutively present in rice roots and leaves. An electrophoretic mobility shift assay and cyclic amplification and selection of targets experiment revealed that IDEF2 predominantly recognized CA(A/C)G(T/C)(T/C/A)(T/C/A) within IDE2 as the core-binding site. IDEF2 belongs to an uncharacterized branch of the NAC transcription factor family and exhibits novel properties of sequence recognition.

We identified a novel transcription factor of rice and barley, IDEF2, which specifically binds to the iron deficiency-responsive cis-acting element 2 (IDE2) by yeast one-hybrid screening. Plants induce iron utilization systems under conditions of low iron availability, but the molecular mechanisms of gene regulation under iron deficiency remain largely unknown. Iron is essential for most living organisms, and thus iron deficiency poses a major abiotic stress in crop production. Glycobiology and Extracellular Matrices.

Srdx core recognition