综合性转录基因分析揭示了番茄植物对Ralstonia solanacearum反应的lncRNA-miRNA-mRNA相互作用
Xiuyang Si1, Hongyan Liu1, Xi Cheng1
1Department of Horticulture, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China.
International journal of biological macromolecules
|September 14, 2023
概括
这项研究揭示了非编码RNAs,包括长非编码RNAs (lncRNAs) 和microRNAs (miRNAs) 如何调节番茄对Ralstonia solanacearum细菌枯的耐药性. 确定了关键的监管网络,为疾病抵抗机制提供了新的见解.
科学领域:
- 植物病理学 植物病理学
- 分子生物学分子生物学
- 基因组学就是基因组学.
- 生物化学 生物化学
背景情况:
- 拉尔斯托尼亚·索拉纳西乌姆 (Ralstonia solanacearum) 导致西红显著的细菌枯,影响全球生产.
- 在番茄对细菌枯的反应中,非编码RNA的作用尚不清楚.
- 了解这些调节机制对于开发抗病番茄品种至关重要.
研究的目的:
- 在R. solanacearum感染后全面分析番茄耐药和易受性线的转录格局.
- 为了识别差异表达的非编码RNAs (lncRNAs,miRNAs) 和参与细菌枯抵抗的mRNAs.
- 阐明非编码RNA,包括ceRNA网络和内源性标模仿物 (eTMs) 在番茄-病原体相互作用中的调节作用.
主要方法:
- 使用高通量RNA测序,在耐药 ('ZRS_7') 和易受 ('HTY_9') 番茄系中分析了mRNA和非编码RNA.
- 进行了差异表达分析,基因本体学 (GO) 和KEGG通路分析.
- 竞争的内源RNA (ceRNA) 网络结构和病毒诱导基因沉默 (VIGS) 技术被用来验证监管相互作用.
主要成果:
- 在注射后,在耐药和易受性线之间观察到数千个mRNA,lncRNA和miRNA的显著变化.
- 基因型特异性反应表明,非编码RNA在疾病耐药性方面具有不同的调节作用.
- 构建了一个复杂的ceRNA网络,涉及miRNAs,lncRNAs和mRNAs,突出了像受体类激酶和NBS-LRRs这样的潜在目标.
- 静止一种内源性标模仿物 (eTM482e-3p-1) 显著增加了番茄的敏感性,证实了它在eTM482e-3p-1-Sly-miR482e-3p-NBS-LRRs调节途径中的作用.
结论:
- 非编码RNAs,特别是lncRNAs和miRNAs,在调节番茄对R. solanacearum的反应中起着至关重要的作用.
- 已识别的ceRNA网络和eTM为细菌枯抵抗的基础分子机制提供了新的见解.
- 这些发现为开发新策略铺平了道路,通过操纵非编码RNA通路来增强番茄病耐药性.
相关概念视频
lncRNA - Long Non-coding RNAs
8.6K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.6K
MicroRNAs
3.0K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.0K
RNA Interference
26.1K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
26.1K
Experimental RNAi
6.2K
RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.2K


