Full- length ATHB17 protein functions as transcriptional repressor and ATHB17Δ113 can relieve repression caused by full-length ATHB17 protein. A. RiceElena KhandelwalAbha A. CreelmanRobert GriffithCara E. AhrensJeffrey Philip TaylorJ. R. MurphyLesley ManjunathSiva L. ThompsonRebecca J. LingardMatthew L. BackStephanie LarueHuachun R. BraytonBonnie J. BurekAmanda TiwariShiv AdamLuc A. MorrellJames A. CaldoRico HuaiQing K. KouadioJean-Louis KuehnRosemarie M. SantAnagha J. WingbermuehleWilliam SalaRodrigo FosterMatt D. KinserJosh MohantyRadha JiangDongming ZieglerTodd E. G. HuangMingya V. KuriakoseSaritha SkottkeKyle P. RepettiPeter Lynne ReuberT. G. RuffThomas E. PetracekMarie J. LoidaPaul 2014 <p>Maize mesophyll protoplasts were transformed (A) with 4 µg cells of reporter (Class II::GUS, Class I::GUS or No BS::GUS) and 0–5 µg cells of effector (Full-length ATHB17) or 5 µg of ATHB17Δ113 and <i>Renilla</i> luciferase (B) with 4 µg reporter (Class II::GUS, Class I::GUS or No BS::GUS), 0–5 µg ATHB17Δ113, and 0 (grey bars) or 0.2 µg (blue bars) of ATHB17 full length. DNA amounts are per 320,000 cells. After 18 h, cells were assayed for GUS and luciferase expression. GUS values were divided by luciferase internal control values for each well and normalized to respective GFP samples. Bars are means and error bars represent 1 SD.</p>