Key Laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Institute of Agro-Bioengineering/College of Life Sciences, Guizhou University, Guiyang 550025, Guizhou, China.
Institute of Pomology Science, Guizhou Academy of Agricultural Sciences, Guiyang 550006, Guizhou, China.
Int J Mol Sci. 2020 May 6;21(9):3288. doi: 10.3390/ijms21093288.
To gain more valuable genomic information about betalain biosynthesis, the full-length transcriptome of pitaya pulp from 'Zihonglong' (red pulp) and 'Jinghonglong' (white pulp) in four fruit developmental stages was analyzed using Single-Molecule Real-Time (SMRT) sequencing corrected by Illumina RNA-sequence (Illumina RNA-Seq). A total of 65,317 and 91,638 genes were identified in 'Zihonglong' and 'Jinghonglong', respectively. A total of 11,377 and 15,551 genes with more than two isoforms were investigated from 'Zihonglong' and 'Jinghonglong', respectively. In total, 156,955 genes were acquired after elimination of redundancy, of which, 120,604 genes (79.63%) were annotated, and 30,875 (20.37%) sequences without hits to reference database were probably novel genes in pitaya. A total of 31,169 and 53,024 simple sequence repeats (SSRs) were uncovered from the genes of 'Zihonglong' and 'Jinghonglong', and 11,650 long non-coding RNAs (lncRNAs) in 'Zihonglong' and 11,113 lncRNAs in 'Jinghonglong' were obtained herein. qRT-PCR was conducted on ten candidate genes, the expression level of six novel genes were consistent with the Fragments Per Kilobase of transcript per Million mapped reads (FPKM) values. In conclusion, we firstly undertook SMRT sequencing of the full-length transcriptome of pitaya, and the valuable resource that was acquired through this sequencing facilitated the identification of additional betalain-related genes. Notably, a list of novel putative genes related to the synthesis of betalain in pitaya fruits was assembled. This may provide new insights into betalain synthesis in pitaya.
为了从龙舌兰科(Agavaceae)石蒜科(Amaryllidaceae)植物果实中获得更多关于甜菜红素生物合成的有价值的基因组信息,利用单分子实时测序(SMRT)对‘紫红龙’(红龙果,紫红色果肉)和‘晶红龙’(白龙果,白色果肉)四个果实发育期的全长转录组进行了测序,并结合 Illumina RNA-seq 测序(Illumina RNA-Seq)进行了校正。分别在‘紫红龙’和‘晶红龙’中鉴定到 65317 个和 91638 个基因。分别对‘紫红龙’和‘晶红龙’中具有两个以上同工型的 11377 个和 15551 个基因进行了研究。总共消除冗余后获得了 156955 个基因,其中 120604 个(79.63%)被注释,30875 个(20.37%)序列没有与参考数据库的匹配,可能是火龙果中的新基因。从‘紫红龙’和‘晶红龙’的基因中分别发现了 31169 个和 53024 个简单序列重复(SSR),并获得了 11650 个长非编码 RNA(lncRNA)在‘紫红龙’中,11113 个 lncRNA 在‘晶红龙’中。对 10 个候选基因进行了 qRT-PCR 分析,6 个新基因的表达水平与片段每百万映射读取数(FPKM)值一致。总之,我们首次对火龙果全长转录组进行了 SMRT 测序,通过该测序获得的有价值的资源促进了甜菜红素相关基因的鉴定。值得注意的是,组装了一组与火龙果果实中甜菜红素合成相关的新推定基因。这可能为火龙果中甜菜红素的合成提供新的见解。