Full-length transcriptome characterization and comparative analysis of Gleditsia sinensis

被引:5
|
作者
Xiao, Feng [1 ]
Zhao, Yang [1 ]
Wang, Xiurong [1 ]
Jian, Xueyan [2 ]
机构
[1] Guizhou Univ, Inst Forest Resources & Environm Guizhou, Coll Forestry, Key Lab Forest Cultivat Plateau Mt Guizhou Prov, Guiyang 550025, Guizhou, Peoples R China
[2] Yanbian Univ, Sch Continuing Educ, Yanji 133002, Jilin, Peoples R China
关键词
Gleditsia sinensis; Comparative transcriptome; PacBio SMRT; Ka/Ks; CODON USAGE; GENES; IDENTIFICATION; PROTEIN;
D O I
10.1186/s12864-023-09843-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
As an economically important tree, Gleditsia sinensis Lam. is widely planted. A lack of background genetic information on G. sinensis hinders molecular breeding. Based on PacBio single-molecule real-time (SMRT) sequencing and analysis of G. sinensis, a total of 95,183 non-redundant transcript sequences were obtained, of which 93,668 contained complete open reading frames (ORFs), 2,858 were long non-coding RNAs (LncRNAs) and 18,855 alternative splicing (AS) events were identified. Genes orthologous to different Gleditsia species pairs were identified, stress-related genes had been positively selected during the evolution. AGA, AGG, and CCA were identified as the universal optimal codon in the genus of Gleditsia. EIF5A was selected as a suitable fluorescent quantitative reference gene. 315 Cytochrome P450 monooxygenases (CYP450s) and 147 uridine diphosphate (UDP)-glycosyltransferases (UGTs) were recognized through the PacBio SMRT transcriptome. Randomized selection of GsIAA14 for cloning verified the reliability of the PacBio SMRT transcriptome assembly sequence. In conclusion, the research data lay the foundation for further analysis of the evolutionary mechanism and molecular breeding of Gleditsia.
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页数:13
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