The phototropic response of Arabidopsis (Arabidopsis thaliana) is induced by the phototropin photoreceptors and modulated by the cryptochrome and phytochrome photoreceptors. Downstream of these photoreceptors, asymmetric lateral redistribution of auxin underlies the differential growth, which results in phototropism. Historical physiological evidence and recent analysis of hormone-induced gene expression demonstrate that auxin and brassinosteroid signaling function interdependently. Similarly, in this study we report evidence that interactions between brassinosteroids and auxin signaling modulate phototropic responsiveness. We found that elongated, a previously identified photomorphogenesis mutant, enhances high-light phototropism and represents a unique allele of BAK1/SERK3, a receptor kinase implicated in brassinosteroid perception. Altogether, our results support the hypothesis that phototropic responsiveness is modulated by inputs that influence control of auxin response factor-mediated transcription.For successful establishment, emerging seedlings rely upon etiolated and tropic growth to maximize light interception. Once the seedling reaches sufficient light to support growth, there is less apparent need to continue elongating rapidly, so photomorphogenesis decreases shoot elongation, expands cotyledons, and promotes chloroplast biogenesis. How changes in signaling associated with photomorphogenesis effect phototropism remains open for investigation. It is clear, however, that photomorphogenesis is not dependent upon phototropism as Arabidopsis (Arabidopsis thaliana) nonphototropic hypocotyl 3 (nph3) mutants display a normal photomorphogenic growth response (Motchoulski and Liscum, 1999;Folta and Spalding, 2001a).Both phototropism and photomorphogenesis are modulated by a common set of photoreceptors. Under unilateral low blue-light conditions (#1.0 mmol m 22 s 21 ), coaction between phototropin (phot1), cryptochrome (cry1 and cry2), and phytochrome (phyA, phyB, and phyD) photoreceptors stimulates or enhances the phototropic response of etiolated seedlings Hangarter, 2003, 2004). Under higher intensity blue light (.1 mmol m 22 s 21 ) from above, these same photoreceptors control growth during photomorphogenesis (Casal, 2000; Spalding, 2001a, 2001b).We previously found that higher intensities of unilateral blue light ($10 mmol m 22 s 21 ) delay the phototropic response of etiolated seedlings (Whippo and Hangarter, 2003). This attenuation of high-light phototropism is mediated by the activities of phot1, phot2, cry1, cry2, and phyA Hangarter, 2003, 2004). Initially, we hypothesized that the slower phototropic response to high-fluence rates of blue light was a secondary consequence of hypocotyl growth inhibition associated with photomorphogenesis (Whippo and Hangarter, 2003). However, we later found that the enhanced high-light phototropic response of specific phytochrome mutants does not always correlate to the inhibition of hypocotyl elongation (Whippo and Hangarter, 2004). This finding raises the possib...