The plants were grown in the field under normal conditions. Petals and anthers were sampled on the day

of flowering, and ovules and fibers were excised from developing flower buds or bolls on selected days post anthesis (DPA). Roots, stems, and leaves were collected from two-week-old seedlings. All tissues collected were quick-frozen in liquid nitrogen and stored at − 70 °C before use. G. hirsutum cultivar Jinmian 19, which exhibits high tolerance to abiotic selleck compound stress, was used for the abiotic stress treatments. Salt and drought stress treatments were applied by immersing the seedlings in 200 mmol L− 1 NaCl and 20% PEG-6000, respectively. The leaves were harvested at appropriate times, quick-frozen in liquid nitrogen, and stored at − 70 °C before use. Gossypium barbadense cultivar Hai 7124, which exhibits Verticillium resistance, was used for fungal pathogen (V. dahliae) inoculation. The roots of Hai 7124 seedlings were dipped in V. dahliae strain VD8 conidial suspensions containing 107 spores mL− 1. The roots were harvested at the appropriate time, quick-frozen in liquid nitrogen, Idelalisib order and stored at − 70 °C before use. Total RNA was isolated according to the method of Jiang

and Zhang [41]. To remove genomic DNA, the RNA samples were treated with DNase I. First-strand cDNA was synthesized based on reverse transcription of 2 μg RNA digested by DNase I using the reverse transcription polymerase reaction system (Promega, USA). For real-time PCR, gene-specific primers were designed based on the WRKY gene sequences using Primer 5.0 (http://www.premierbiosoft.com/). The amplified fragment length ranged from 75 bp to 200 bp, and the annealing temperature ranged from 58 °C to 60 °C. The cotton histone3 (AF024716) gene (forward primer and reverse primer sequences 5′-GAAGCCTCATCGATACCGTC-3′ and 5′-CTACCACTACCATCATGG-3′, respectively) was used as the reference gene [19]. The amplification reactions of the real-time PCR were performed using an ABI 7500 real-time why PCR system. The amplification parameters were as follows: denaturation at 95 °C for 10 min, 40 cycles

of denaturation at 95 °C for 15 s, annealing at 58–60 °C for 15 s, and extension at 72 °C for 15 s. For the melting curve stage, the default settings were chosen. Three biological replicates, each with three technical replicates, were tested. The expression levels of the WRKY genes were calculated according to Livak and Schmittgen [42]. Based on bioinformatic analysis, gene-specific PCR primer pairs were individually designed for PCR-amplification of the WRKY genes based on the complete ORF cDNA sequences ( Table S1), and the transcripts from various tissues of G. hirsutum acc. TM-1 were used for amplification. Standard PCR analysis was performed using High-Fidelity ExTaq DNA Polymerase [TaKaRa Biotechnology (Dalian) Co., Ltd., China].