Hen changing root hair and primary root growth and up-regulating HAK5 expression in Arabidopsis [13]. Moreover, many genes respond to K starvation, which leads to increased pathogen susceptibility; a process that is linked to jasmonic acid [9]. The cytokinins (CKs) regulate various processes within plants, including cell division and root and shoot morphogenesis. In Arabidopsis, the key CK biosynthetic enzymes are adenosine phosphate-isopentenyltransferases (IPTs) [14]. There are twoCytokinins Regulate Low K Signalingclasses of IPTs in Arabidopsis. ATP/ADP IPTs are involved in the synthesis of N6-(D2-isopentenyl)adenine (iP)- and trans-zeatin (tZ)type CKs, whereas tRNA IPTs are responsible for the biosynthesis of cis-zeatin (cZ)-type CKs [14]. Additionally, it was suggested that the iP- and tZ-type CKs are the major forms and are more physiologically active than PS 1145 chemical information cZ-type CKs in Arabidopsis [15]. To exert their MedChemExpress PTH 1-34 biological functions, CK signaling is mediated by a multi-step phosphorelay that consists of CK receptor histidine kinases (AHKs), phosphotransfer proteins (AHPs) and response regulators (ARRs). The AHKs respond to CKs by autophosphorylation and transfer of a phosphoryl group to the ARRs through the AHPs, resulting in the activation of downstream proteins [16]. Among the 8 AHKs, AHK2, AHK3 and AHK4 are implicated in CK signaling [16,17]. It is fairly well known that interactions between nutrients and CKs influence nutrient signaling and adaptive responses in plants. Nitrate treatment induces the biosynthesis of CKs by up-regulating IPT3 [18] and also triggers the expression of type-A ARRs in Arabidopsis [19]. CKs are also linked systemically to phosphate deprivation signaling by repressing the expression of genes that are induced by phosphate starvation conditions [20]. Through characterization of plants carrying mutations in the receptor kinases AHK3 and AHK4, it was revealed that these kinase encoding genes contribute to the repression of phosphatestarvation-responsive genes [21]. In addition, CKs were found to exert a negative effect on expression of SULTR1;1 and SULTR1;2, resulting in a reduction of sulfate uptake in roots [22]. AHK3 and AHK4 are also involved in the root iron uptake machinery in Arabidopsis by negatively regulating the expression of genes which are induced by iron deficiency [23]. Taken together, these studies demonstrate that CKs play a role in 
the response to the limitations of various nutrients in plants. However, 
the roles of CKs in low K signaling are still unclear at the present time. Here, we show that CK receptor mutants lose their responsiveness to low K signaling through the measurement of ROS accumulation and root growth under low K conditions. Additionally, we found that CKs affected the induction of HAK5 expression and function under low K conditions. Finally, we provide evidence that CKs negatively regulate low K response.CK MeasurementsFor measuring CK content, four-day-old seedlings were transferred to +K or 2K LSM, and then the roots and shoots from Arabidopsis grown in either +K or 2K conditions for 1, 3 or 7 days were harvested. More than 6 replicates per condition were analyzed. Extraction and determination of CKs were performed as previously described [25]. Statistical differences were evaluated with a t-test using the Graphpad Prism 5.01 software program.Root AssayAll seeds were planted on normal LSM and vernalized at 4uC for 3 days. Four-day-old seedlings were transferred to +K or 2K med.Hen changing root hair and primary root growth and up-regulating HAK5 expression in Arabidopsis [13]. Moreover, many genes respond to K starvation, which leads to increased pathogen susceptibility; a process that is linked to jasmonic acid [9]. The cytokinins (CKs) regulate various processes within plants, including cell division and root and shoot morphogenesis. In Arabidopsis, the key CK biosynthetic enzymes are adenosine phosphate-isopentenyltransferases (IPTs) [14]. There are twoCytokinins Regulate Low K Signalingclasses of IPTs in Arabidopsis. ATP/ADP IPTs are involved in the synthesis of N6-(D2-isopentenyl)adenine (iP)- and trans-zeatin (tZ)type CKs, whereas tRNA IPTs are responsible for the biosynthesis of cis-zeatin (cZ)-type CKs [14]. Additionally, it was suggested that the iP- and tZ-type CKs are the major forms and are more physiologically active than cZ-type CKs in Arabidopsis [15]. To exert their biological functions, CK signaling is mediated by a multi-step phosphorelay that consists of CK receptor histidine kinases (AHKs), phosphotransfer proteins (AHPs) and response regulators (ARRs). The AHKs respond to CKs by autophosphorylation and transfer of a phosphoryl group to the ARRs through the AHPs, resulting in the activation of downstream proteins [16]. Among the 8 AHKs, AHK2, AHK3 and AHK4 are implicated in CK signaling [16,17]. It is fairly well known that interactions between nutrients and CKs influence nutrient signaling and adaptive responses in plants. Nitrate treatment induces the biosynthesis of CKs by up-regulating IPT3 [18] and also triggers the expression of type-A ARRs in Arabidopsis [19]. CKs are also linked systemically to phosphate deprivation signaling by repressing the expression of genes that are induced by phosphate starvation conditions [20]. Through characterization of plants carrying mutations in the receptor kinases AHK3 and AHK4, it was revealed that these kinase encoding genes contribute to the repression of phosphatestarvation-responsive genes [21]. In addition, CKs were found to exert a negative effect on expression of SULTR1;1 and SULTR1;2, resulting in a reduction of sulfate uptake in roots [22]. AHK3 and AHK4 are also involved in the root iron uptake machinery in Arabidopsis by negatively regulating the expression of genes which are induced by iron deficiency [23]. Taken together, these studies demonstrate that CKs play a role in the response to the limitations of various nutrients in plants. However, the roles of CKs in low K signaling are still unclear at the present time. Here, we show that CK receptor mutants lose their responsiveness to low K signaling through the measurement of ROS accumulation and root growth under low K conditions. Additionally, we found that CKs affected the induction of HAK5 expression and function under low K conditions. Finally, we provide evidence that CKs negatively regulate low K response.CK MeasurementsFor measuring CK content, four-day-old seedlings were transferred to +K or 2K LSM, and then the roots and shoots from Arabidopsis grown in either +K or 2K conditions for 1, 3 or 7 days were harvested. More than 6 replicates per condition were analyzed. Extraction and determination of CKs were performed as previously described [25]. Statistical differences were evaluated with a t-test using the Graphpad Prism 5.01 software program.Root AssayAll seeds were planted on normal LSM and vernalized at 4uC for 3 days. Four-day-old seedlings were transferred to +K or 2K med.
