In the barley (Hordeum vulgare) Hooded (Kap) mutant, the duplication of a 305-bp intron sequence leads to the overexpression of the Barley knox3 (Bkn3) gene, resulting in the development of an extra flower in the spikelet. We used a one-hybrid screen to identify four proteins that bind the intron-located regulatory element (Kap intron-binding proteins). Three of these, Barley Ethylene Response Factor1 (BERF1), Barley Ethylene Insensitive Like1 (BEIL1), and Barley Growth Regulating Factor1 (BGRF1), were characterized and their in vitro DNA-binding capacities verified. Given the homology of BERF1 and BEIL1 to ethylene signaling proteins, we investigated if these factors might play a dual role in intron-mediated regulation and ethylene response. In transgenic rice (Oryza sativa), constitutive expression of the corresponding genes produced phenotypic alterations consistent with perturbations in ethylene levels and variations in the expression of a key gene of ethylene biosynthesis. In barley, ethylene treatment results in partial suppression of the Kap phenotype, accompanied by up-regulation of BERF1 and BEIL1 expression, followed by down-regulation of Bkn3 mRNA levels. In rice protoplasts, BEIL1 activates the expression of a reporter gene driven by the 305-bp intron element, while BERF1 can counteract this activation. Thus, BEIL1 and BERF1, likely in association with other Kap intron-binding proteins, should mediate the fine-tuning of Bkn3 expression by ethylene. We propose a hypothesis for the cross talk between the KNOX and ethylene pathways.Organogenesis in plants is a continuous process involving meristems, populations of pluripotent cells. The shoot apical meristem (SAM) is formed during embryogenesis and initiates organ primordia in postembryonic growth. SAM activity entails two contrasting processes: the slow proliferation of cells in the central zone, necessary for meristem maintenance, and the recruitment of cells at the meristem flanks, where lateral organ primordia are initiated (Scofield and Murray, 2006).Knotted1-like homeobox (KNOX) genes represent an ancient class of transcription factors present in all examined plant species as well as in single-cell green and red algae (Mukherjee et al., 2009). A subset of this gene family (class I KNOX genes) regulates SAM functions in both monocots and dicots. KNOX I genes play pivotal roles not only in SAM formation and maintenance but also in morphogenetic processes throughout plant development (Hake et al., 2004): they contribute to cell fate and cell differentiation of vegetative (Vollbrecht et al., 1991;Becraft and Freeling, 1994) and reproductive (Mü ller et al., 1995; WilliamsCarrier et al., 1997) tissues.KNOX I genes encode transcription factors belonging to the TALE-homeobox superfamily (Bü rglin,