Full-length SMRT transcriptome sequencing and microsatellite characterization in Paulownia catalpifolia

被引:12
|
作者
Feng, Yanzhi [1 ,2 ,3 ,4 ]
Zhao, Yang [1 ,2 ,3 ,4 ]
Zhang, Jiajia [1 ,2 ,3 ,4 ]
Wang, Baoping [1 ,2 ,3 ,4 ]
Yang, Chaowei [1 ,2 ,3 ,4 ]
Zhou, Haijiang [1 ,2 ,3 ,4 ]
Qiao, Jie [1 ,2 ,3 ,4 ]
机构
[1] Paulownia Res & Dev Ctr State Adm Forestry & Gras, Zhengzhou 450003, Peoples R China
[2] Chinese Acad Forestry, Nontimber Forestry Res & Dev Ctr, Zhengzhou 450003, Peoples R China
[3] Key Lab Nontimber Forest Germplasm Enhancement &, Zhengzhou 450003, Peoples R China
[4] Natl Innovat Alliance Paulownia, Zhengzhou 450003, Peoples R China
关键词
EST-SSR MARKERS; CROSS-SPECIES/GENERA TRANSFERABILITY; GENE-EXPRESSION; GENOME; COMPLEXITY; ISOFORMS; L;
D O I
10.1038/s41598-021-87538-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Paulownia catalpifolia is an important, fast-growing timber species known for its high density, color and texture. However, few transcriptomic and genetic studies have been conducted in P. catalpifolia. In this study, single-molecule real-time sequencing technology was applied to obtain the full-length transcriptome of P. catalpifolia leaves treated with varying degrees of drought stress. The sequencing data were then used to search for microsatellites, or simple sequence repeats (SSRs). A total of 28.83 Gb data were generated, 25,969 high-quality (HQ) transcripts with an average length of 1624 bp were acquired after removing the redundant reads, and 25,602 HQ transcripts (98.59%) were annotated using public databases. Among the HQ transcripts, 16,722 intact coding sequences, 149 long non-coding RNAs and 179 alternative splicing events were predicted, respectively. A total of 7367 SSR loci were distributed throughout 6293 HQ transcripts, of which 763 complex SSRs and 6604 complete SSRs. The SSR appearance frequency was 28.37%, and the average distribution distance was 5.59 kb. Among the 6604 complete SSR loci, 1-3 nucleotide repeats were dominant, occupying 97.85% of the total SSR loci, of which mono-, di- and tri-nucleotide repeats were 44.68%, 33.86% and 19.31%, respectively. We detected 112 repeat motifs, of which A/T (42.64%), AG/CT (12.22%), GA/TC (9.63%), GAA/TTC (1.57%) and CCA/TGG (1.54%) were most common in mono-, di- and tri-nucleotide repeats, respectively. The length of the repeat SSR motifs was 10-88 bp, and 4997 (75.67%) were <= 20 bp. This study provides a novel full-length transcriptome reference for P. catalpifolia and will facilitate the identification of germplasm resources and breeding of new drought-resistant P. catalpifolia varieties.
引用
收藏
页数:12
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