De novo sequencing and transcriptome assembly of Arisaema heterophyllum Blume and identification of genes involved in isoflavonoid biosynthesis

被引:19
|
作者
Wang, Chenkai [1 ,2 ,4 ]
Zhu, Jinhang [3 ]
Liu, Miaomiao [1 ,2 ,4 ]
Yang, Qingshan [1 ,2 ,5 ]
Wu, Jiawen [1 ,2 ,4 ,5 ]
Li, Zegeng [1 ,2 ,6 ,7 ]
机构
[1] Anhui Univ Chinese Med, Hefei 230032, Anhui, Peoples R China
[2] Anhui Acad Chinese Med, Hefei 230038, Anhui, Peoples R China
[3] Anhui Med Univ, Hefei 230032, Anhui, Peoples R China
[4] Anhui Univ Chinese Med, Key Lab Xinan Med, Minist Educ, Hefei 230038, Anhui, Peoples R China
[5] Synerget Innovat Ctr Anhui Authent Chinese Med Qu, Hefei 230012, Anhui, Peoples R China
[6] Anhui Univ Tradit Chinese Med, Affiliated Hosp 1, Hefei 230038, Anhui, Peoples R China
[7] State Adm Tradit Chinese Med Peoples Republ China, Key Lab Resp Dis, Hefei 230038, Anhui, Peoples R China
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
中国国家自然科学基金;
关键词
EST-SSR MARKERS; MICROSATELLITE MARKERS; CONSTRUCTION; ANNOTATION; EXPRESSION; FRUIT; TOOL;
D O I
10.1038/s41598-018-35664-1
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
Arisaema heterophyllum Blume (AhBl) is one of the valued medicinal plants. However, its genetic information is limited, which impedes further studies of this valuable resource. To investigate the genes involved in the isoflavonoid biosynthesis, we deeply performed transcriptome sequencing for AhBl. An average of 10.98 Gb clean reads were obtained based on root, tuber and leaf tissues, and 109,937 unigenes were yielded after de novo assembly. In total, 72,287 of those unigenes were annotated in at least one public database. The numbers of expressed unigenes in each tissue were 35,686, 43,363 and 47,783, respectively. The overall expression levels of transcripts in leaf were higher than those in root and tuber. Differentially expressed genes analysis indicated that a total of 12,448 shared unigenes were detected in all three tissues, 10,215 of which were higher expressed in tuber than that in root and leaf. Besides, 87 candidate unigenes that encode for enzymes involved in biosynthesis of isoflavonoid were identified and analyzed, and some key enzyme genes were experimentally validated by quantitative Real-Time PCR (qRT-PCR). This study provides a unique dataset for the systematic analysis of AhBl functional genes and expression characteristics, and facilitates the future study of the pharmacological mechanism of AhBl.
引用
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页数:12
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