Several members of the AGCVIII kinase subfamily, which includes PINOID (PID), PID2, and WAVY ROOT GROWTH (WAG) proteins, have previously been shown to phosphorylate PIN-FORMED (PIN) auxin transporters and control the auxin flow in plants. PID has been proposed as a key component of the phototropin signaling pathway that induces phototropic responses, although the responses were not significantly impaired in the pid single and pid wag1 wag2 triple mutants. This raises questions about the functional roles of the PID family in phototropic responses. Here, we investigated hypocotyl phototropism in the pid pid2 wag1 wag2 quadruple mutant in detail to clarify the roles of the PID family in Arabidopsis (Arabidopsis thaliana). The pid quadruple mutants exhibited moderate responses in continuous light-induced phototropism with a decrease in growth rates of hypocotyls and normal responses in pulse-induced phototropism. However, they showed serious defects in enhancements of pulse-induced phototropic curvatures and lateral fluorescent auxin transport by red light pretreatment. Red light pretreatment significantly reduced the expression level of PID, and the constitutive expression of PID prevented pulse-induced phototropism, irrespective of red light pretreatment. This suggests that the PID family plays a significant role in phytochrome-mediated phototropic enhancement but not the phototropin signaling pathway. Red light treatment enhanced the intracellular accumulation of PIN proteins in response to the vesicle-trafficking inhibitor brefeldin A in addition to increasing their expression levels. Taken together, these results suggest that red light preirradiation enhances phototropic curvatures by upregulation of PIN proteins, which are not being phosphorylated by the PID family.Sessile organisms, such as plants, develop many adaptational mechanisms. Phototropism is one such acclimation response in plants to light environments, by which they can advantageously obtain light energy for photosynthesis. So far, phototropic responses, which have been well studied for many years, are separated mainly into two types according to their characters: the first positive phototropism and the second positive phototropism (Iino, 2001;Whippo and Hangarter, 2006;Briggs, 2014). The first positive phototropism is induced by a pulse of blue light, and the magnitudes of the responses are dependent totally on the total light fluence. However, the second positive phototropism is induced by a prolonged irradiation of blue light, and the extent of the curvature responses depends on the duration of the blue light illumination and not on the total light fluences.Classical physiological analysis has revealed that plant photoreceptor phytochromes influence phototropin (phot)-mediated phototropic responses in several aspects (Iino, 2001;Whippo and Hangarter, 2006;Sakai and Haga, 2012;Briggs, 2014). For the first positive pulse-induced phototropism, phytochromes are involved in the enhancement of phototropic curvatures in addition to desensitization (Liu...