“…The primers used in our experiment amplified specifically for the following genes: glucosyltransferases UGT73C1 , UGT73C5 , UGT76C1 , UGT76C2 , UGT85A1 ; CK dehydrogenases CKX1 - 7 ; isopentenyltransferases IPT1-9 ; CK nucleoside 5′-monophosphate phosphoribohydrolase LOG2 , LOG8 ; CK trans -hydroxylase CYP735A2 ; response regulators type A ( ARR5 , ARR15 , ARR16 ), type B ( ARR1 , ARR2 , ARR10 , ARR14 ); CK receptors AHK4 , AHK2 , AHK3 . All the listed primers were designed according to our previously published work (Mik et al, 2011; Motte et al, 2013; also see Supplementary material of these publications for details), Rubisco small chain RUBsc (Hensel et al, 1993), cysteine protease senescence-associated gene SAG12 (Gepstein et al, 2003; Wagstaff et al, 2009) and chlorophyll a/b binding protein CAB2 (Kim et al, 2006), for transcription factors MYB2 (Guo and Gan, 2011) and WRKY53 (Hinderhofer and Zentgraf, 2001; Balazadeh et al, 2008); for 1-aminocyklopropan-1-carboxylate synthase ACS8 as a key regulatory enzyme in the biosynthesis of the plant hormone ethylene (Tian et al, 2009); for chalcone flavanone isomerase CHI as anthocyanins biosynthetic enzyme (Catala et al, 2011); 9- cis -epoxycarotenoid dioxygenase NCED3 , a key enzyme in the biosynthesis of abscisic acid (Tan et al, 2003). RNA from three biological replicates was transcribed in at least two independent reactions and each cDNA sample was run in at least three technical replications on Viia7 TM Real-Time PCR System in a default program (Life Technologies).…”