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茉莉酸甲酯诱导24小时后叶片中的差异基因表达分析

Differential Gene Expression Analysis in Leaf upon 24 h of Methyl Jasmonate Elicitation.

作者信息

Rahnamaie-Tajadod Reyhaneh, Loke Kok-Keong, Goh Hoe-Han, Noor Normah M

机构信息

Institute of Systems Biology (INBIOSIS), Universiti Kebangsaan Malaysia Bangi, Malaysia.

出版信息

Front Plant Sci. 2017 Feb 6;8:109. doi: 10.3389/fpls.2017.00109. eCollection 2017.

Abstract

is an herbal plant that grows in Southeast Asian countries and traditionally used as medicine. This plant produces diverse secondary metabolites such as phenolic compounds and their derivatives, which are known to have roles in plant abiotic and biotic stress responses. Methyl jasmonate (MeJA) is a plant signaling molecule that triggers transcriptional reprogramming in secondary metabolism and activation of defense responses against many biotic and abiotic stresses. However, the effect of MeJA elicitation on the genome-wide expression profile in the leaf tissue of has not been well-studied due to the limited genetic information. Hence, we performed Illumina paired-end RNA-seq for reconstruction of leaf transcriptome to identify differentially expressed genes (DEGs) in response to MeJA elicitation. A total of 182,111 unique transcripts (UTs) were obtained by assembly of 191.57 million paired-end clean reads using Trinity analysis pipeline. A total of 2374 UTs were identified to be significantly up-/down-regulated 24 h after MeJA treatment. These UTs comprising many genes related to plant secondary metabolite biosynthesis, defense and stress responses. To validate our sequencing results, we analyzed the expression of 21 selected DEGs by quantitative real-time PCR and found a good correlation between the two analyses. The single time-point analysis in this work not only provides a useful genomic resource for but also gives insights on molecular mechanisms of stress responses in .

摘要

是一种生长在东南亚国家的草本植物,传统上用作药物。这种植物产生多种次生代谢产物,如酚类化合物及其衍生物,已知它们在植物非生物和生物胁迫反应中发挥作用。茉莉酸甲酯(MeJA)是一种植物信号分子,可触发次生代谢中的转录重编程,并激活针对许多生物和非生物胁迫的防御反应。然而,由于遗传信息有限,MeJA诱导对[植物名称]叶片组织全基因组表达谱的影响尚未得到充分研究。因此,我们进行了Illumina双末端RNA测序,以重建[植物名称]叶片转录组,以鉴定响应MeJA诱导的差异表达基因(DEG)。使用Trinity分析管道对1.9157亿对双末端清洁读数进行组装,共获得182,111个独特转录本(UT)。在MeJA处理24小时后,共鉴定出2374个UT显著上调/下调。这些UT包含许多与植物次生代谢产物生物合成、防御和胁迫反应相关的基因。为了验证我们的测序结果,我们通过定量实时PCR分析了21个选定DEG的表达,发现两种分析之间具有良好的相关性。这项工作中的单时间点分析不仅为[植物名称]提供了有用的基因组资源,还深入了解了[植物名称]胁迫反应的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f66/5292430/c0fea834471e/fpls-08-00109-g0001.jpg

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