8Melon (Cucumis melo L.) is wildly planted in the world and China is a major producer of muskmelon.
9Powdery mildew is one of the most common fungal diseases in the world and this disease frequently 1 7 materials were identified. All the DEGs were annotated with several database and the transcript factors 1 8 (TFs) that related to disease resistance such as MYB, ERF and WRKY among the DEGs were also 1 9identified. This research could not only provide the information about understanding the mechanism of 2 0 powdery mildew infection but also help researchers breed the varieties with powdery mildew 2 1 resistance.
2Key words Melon (Cucumis melo L.). powdery mildew. Transcript sequencing. Candidate genes. 2 3 Transcript factors 2 4 4 1 were selected. After inoculating the powdery mildew, both materials were used to do the RNA-Seq. In 4 2 total, two RNA-seq libraries were constructed and sequenced separately; generating 47,462,015 mean 4 3 clean reads with mean GC content of 49.32 and mean Q30 of 85.89%. Among all the genes in the 4 4 genome of melon, 13828 genes were expressed in the material G and 13944 genes were expressed in 4 5 the material S (RPKM>1). Through multiple comparisons between libraries, 769 DEGs were identified, 4 6 of which the 726 were up-regulated DEGs and 43 were down-regulated ones. Based on the annotation 4 7 information in gene ontology (GO), kyoto encyclopedia of genes and genomes (KEGG) and eukaryotic 4 8 orthologous groups (KOG) database, most of the DEGs were related to "nucleus", "chloroplast" and 4 9 7 7 paired-end (PE) raw reads (Personalbio, Shanghai, China). Raw data (raw reads) in FASTQ format 7 8were processed used the trimmomatic software (Bolger et al., 2014). In this step, clean data were 7 9 obtained as follows: the first, removing reads with ≥ 10% unidentified nucleotides (N); the second,
0Removing reads with > 50% bases having phred quality < 5; the third, Removing reads with > 10 nt 8 1 aligned to the adapter, allowing ≤ 10% mismatches; the fourth, removing putative PCR duplicates 8 2 generated by PCR amplification in the library construction process. After trimmomatic, the quality of the clean data was checked by the software FASTQC 3 0 8 3 0 9