De Novo Assembly and Annotation of the Juvenile Tuber Transcriptome of aGastrodia elataHybrid by RNA Sequencing: Detection of SSR Markers

被引:7
作者
Wang, Yunsheng [1 ]
Shahid, Muhammad Qasim [2 ,3 ]
Ghouri, Fozia [2 ,3 ]
Baloch, Faheem Shehzad [4 ]
机构
[1] Kaili Univ, Coll Life & Hlth Sci, Kaili City 556011, Guizhou, Peoples R China
[2] South China Agr Univ, State Key Lab Conservat & Utilizat Subtrop Agrobi, Guangzhou 510642, Peoples R China
[3] South China Agr Univ, Guangdong Prov Key Lab Plant Mol Breeding, Guangzhou 510642, Peoples R China
[4] Abant Izzet Baysal Univ, Fac Agr & Nat Sci, Dept Field Crops, Bolu, Turkey
关键词
Gastrodia elata; Sequencing; SSR; Transcriptome; Unigenes; GASTRODIA-ELATA BLUME; RADICAL SCAVENGING ACTIVITIES; 4-HYDROXYBENZYL ALCOHOL; MOLECULAR MARKERS; MEDICINAL-PLANT; AVOIDANCE TASK; SEQ; DATABASE; IDENTIFICATION; BIOSYNTHESIS;
D O I
10.1007/s10528-020-09983-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gastrodia elatais a traditional Chinese herbal medicine with good therapeutic effect on various nervous and cerebrovascular diseases. In the present study, we generated 20,611,556 raw reads from the young tuber transcriptome of aG. elatahybrid (Gastrodia elata BI.f.elata x Gastrodia elata BI.f.pilifera) by using Illumina HiSeq (TM) 4000 sequencing platform. De novo assembly and bioinformatics analysis revealed 20,237,474 clean reads, including 2,529,684,250 bp that assembled into 34,323 unigenes with an average length of 695.19 bp. Among them, 24,698 (71.96%) unigenes were annotated by at least one of the Nr, Swiss-Prot, COG and KEGG databases. A total of 4236 (12.34%) unigenes were identified as candidate transcription factors, and 2007 (5.85%) unigenes were found to contain at least one single sequence repeat (SSR). Of these SSRs, AG/CT repeat motif was the most frequent, with a total of 498 (21.67%). This study will enhance our understanding about the molecular mechanism of physiological metabolism, growth and development ofG. elata, particularly abundant SSR markers will offer plenty of alternative tools for further studies about molecular genetics, molecular breeding and association analysis.
引用
收藏
页码:914 / 934
页数:21
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