Cytokinin is a phytohormone that is well known for its roles in numerous plant growth and developmental processes, yet it has also been linked to abiotic stress response in a less defined manner. Arabidopsis (Arabidopsis thaliana) Cytokinin Response Factor 6 (CRF6) is a cytokinin-responsive AP2/ERF-family transcription factor that, through the cytokinin signaling pathway, plays a key role in the inhibition of dark-induced senescence. CRF6 expression is also induced by oxidative stress, and here we show a novel function for CRF6 in relation to oxidative stress and identify downstream transcriptional targets of CRF6 that are repressed in response to oxidative stress. Analysis of transcriptomic changes in wild-type and crf6 mutant plants treated with H 2 O 2 identified CRF6-dependent differentially expressed transcripts, many of which were repressed rather than induced. Moreover, many repressed genes also show decreased expression in 35S:CRF6 overexpressing plants. Together, these findings suggest that CRF6 functions largely as a transcriptional repressor. Interestingly, among the H 2 O 2 repressed CRF6-dependent transcripts was a set of five genes associated with cytokinin processes: (signaling) ARR6, ARR9, ARR11, (biosynthesis) LOG7, and (transport) ABCG14. We have examined mutants of these cytokinin-associated target genes to reveal novel connections to oxidative stress. Further examination of CRF6-DNA interactions indicated that CRF6 may regulate its targets both directly and indirectly. Together, this shows that CRF6 functions during oxidative stress as a negative regulator to control this cytokinin-associated module of CRF6-dependent genes and establishes a novel connection between cytokinin and oxidative stress response.The frequent environmental changes to which a plant is subject can lead to physiological alterations and disruption of normal metabolism. In particular, the energetic reactions that take place in chloroplasts, peroxisomes, and mitochondria are susceptible to dysfunction, which results in production of excessive levels of reactive oxygen species (ROS). In fact, many common abiotic stress conditions encountered in agriculture, including temperature extremes, drought, soil salinity, and air pollution, are known to include an oxidative stress component (Gill and Tuteja, 2010). Cellular levels of ROS are carefully maintained at relatively low levels through a wide range of scavenging and detoxification mechanisms. However, if the balance between ROS production and removal is shifted too far toward production (e.g. under stress conditions), cellular damage can occur as a result of oxidation of macromolecules such as lipids, proteins, and nucleic acids (Mittler, 2002;Gill and Tuteja, 2010). Accumulation of ROS beyond some threshold triggers cell death as a response. Therefore, ROS are thought to serve as indicators of oxidative stress within a cell but may also