Petal samples of GB_Pe, WF_Pe and YF_Pe were collected and three independent biological replicates were used. Total RNA was extracted from plant tissue using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s protocol and digested with DNase I (Takara, Dalian, China). The quality and purity of total RNA were evaluated by stringent RNA quality control. cDNA library construction and sequencing were performed by Annoroad Gene Technology (Beijing, China). Each constructed cDNA library (∼10 ng) was subjected to paired-end 150 bp sequencing on an Illumina HiSeq™ 4000 system (San Diego, CA, USA) according to the manufacturer’s instructions.

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