Identification of the Genome-Wide Expression Patterns of Non-Coding RNAs Associated with Tanshinones Synthesis Pathway in Salvia miltiorrhiza

丹参 苯丙素 代谢途径 小桶 生物 基因 基因表达 生物途径 信号转导 生物合成 生物化学 转录组 细胞生物学 病理 中医药 医学 替代医学
作者
Caicai Lin,Changhao Zhou,Zhongqian Liu,Xingfeng Li,Zhenqiao Song
出处
期刊:Agronomy [Multidisciplinary Digital Publishing Institute]
卷期号:13 (2): 321-321 被引量:4
标识
DOI:10.3390/agronomy13020321
摘要

The red root of Salvia miltiorrhiza Bunge, a famous traditional Chinese medicine (TCM), was caused by tanshinone in epidermis cells. In order to study the biological function of ncRNAs in the tanshinone synthesis, the expression patterns of mRNA and ncRNAs were comprehensively analyzed in red (high tanshinone content) and white root (low tanshinone content) tissues derived from the same plant. A total of 731 differentially expressed genes (DEGs) were mainly enriched in primary metabolic pathways such as galactose and nitrogen, and some secondary metabolic pathways such as phenylpropanoid and terpenoids. A total of 70 miRNAs, 48 lncRNAs, and 26 circRNAs were identified as differentially expressed (DE) ones. The enrichment pathway of the targets of DE-lncRNA were mainly in ribosome, carbon metabolism, plant hormone signal transduction, and glycerophospholipid metabolism. The function of the targets genes of 59 miRNAs combined with DE-circRNAs was mainly involved in plant–pathogen interaction, endocytosis, phenylpropanoid biosynthesis, and sesquiterpenoid and triterpenoid biosynthesis pathways. Most genes of the tanshinone synthesis pathway had a higher expression. Some ncRNAs were predicted to regulate several key enzyme genes of the tanshinone synthesis pathway, such as SmDXS2, SmGGPPS1, SmKSL. Furthermore, most target genes were related to the resistance of pathogens. The present study exhibited the tissue-specific expression patterns of ncRNAs, which would provide a basis for further research into the regulation mechanism of ncRNAs in the tanshinone synthesis process.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Silence完成签到 ,获得积分10
1秒前
nczpf2010完成签到,获得积分10
1秒前
1秒前
思源应助开心的秋采纳,获得10
2秒前
混个毕业完成签到,获得积分10
4秒前
whisper完成签到,获得积分10
4秒前
蜗牛爱学习完成签到 ,获得积分10
4秒前
af发布了新的文献求助10
4秒前
vagrant完成签到,获得积分10
5秒前
5秒前
124完成签到,获得积分10
5秒前
豆子发布了新的文献求助10
6秒前
zyb完成签到 ,获得积分10
7秒前
Gauss完成签到,获得积分0
8秒前
万叶完成签到,获得积分10
9秒前
一只鱼发布了新的文献求助10
9秒前
小鹿发布了新的文献求助10
9秒前
happyrrc完成签到,获得积分10
9秒前
fishswim1完成签到,获得积分10
10秒前
此时此刻完成签到 ,获得积分10
10秒前
汉堡包应助ZL采纳,获得10
11秒前
zimu012完成签到 ,获得积分10
11秒前
YIQISUDA完成签到,获得积分10
12秒前
文文武完成签到 ,获得积分10
12秒前
赖晨靓完成签到 ,获得积分10
14秒前
木马上市完成签到,获得积分10
14秒前
传奇3应助积极的珊采纳,获得10
14秒前
研友_Lpa2On完成签到,获得积分20
14秒前
Ecokarster完成签到,获得积分10
15秒前
可爱的梦菲完成签到,获得积分10
15秒前
15秒前
豆子完成签到,获得积分10
17秒前
xiaobin发布了新的文献求助10
17秒前
诚心天晴完成签到 ,获得积分10
18秒前
123asd完成签到 ,获得积分10
19秒前
20秒前
20秒前
兴奋小丸子完成签到,获得积分10
20秒前
21秒前
当女遇到乔完成签到 ,获得积分0
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Handbuch Trainingswissenschaft – Trainingslehre 500
Additive Manufacturing Design and Applications (ASM Handbook, Volume 24A) 500
Variations: A More Diverse Picture of Contemporary Art 400
A Primer on Partial Least Squares Structural Equation Modeling (PLS-SEM) Fourth Edition 400
Induction Heating and Heat Treatment (ASM Handbook, Volume 4C) 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7586541
求助须知:如何正确求助?哪些是违规求助? 9164782
关于积分的说明 19613289
捐赠科研通 7167032
什么是DOI,文献DOI怎么找? 3266670
关于科研通互助平台的介绍 2431693
邀请新用户注册赠送积分活动 2258455