转录组分析显示,在米的OsRpp30介导的疾病耐药性中,有IncRNA-miRNA-mRNA调节网络
Minghua Li1, Wei Li2, Meixia Zhao3
1Department of Biology, Miami University, Oxford, OH, 45056, USA.
BMC genomics
|October 26, 2023
概括
长非编码RNAs (lncRNAs) 对大米免疫非常重要. 这项研究揭示了 lncRNAs.
科学领域:
- 植物分子生物学 植物分子生物学
- 植物病理学 植物病理学
- 基因组学和转录基因组学
背景情况:
- 长非编码RNAs (lncRNAs) 是植物生物过程的组成部分,包括疾病耐药性.
- 米树的RNase P蛋白30 (OsRpp30) 是已知的对抗病原体的米免疫力的积极调节者.
- 在OsRpp30介导的病耐药性中,lncRNAs的具体作用尚不清楚.
研究的目的:
- 综合分析不同OsRpp30水平 (野生类型,过度表达和淘汰赛) 的米植物中的lncRNA,miRNA和mRNA的表达模式.
- 调查lncRNAs和mRNAs之间的调控相互作用,包括跨和cis向.
- 构建一个竞争的内源RNA (ceRNA) 网络,以阐明lncRNAs,miRNAs和mRNAs在米病耐药性的相互作用.
主要方法:
- 使用高通量RNA测序,对野生类型,OsRpp30-OE和OsRpp30-KO大米系中的lncRNA,miRNA和mRNA表达进行了分析.
- 进行生物信息分析以识别差异表达基因 (DEG) 和预测lncRNA-mRNA相互作用 (跨和 cis向).
- 一个ceRNA网络被构建以整合lncRNA,miRNA和mRNA调节关系.
主要成果:
- 在分析的米系中,鉴定出91个差异表达的lncRNAs (DElncRNAs),1671个DEmRNAs和41个DEmiRNAs.
- 发现了10个跨向的lncRNA-mRNA对和27个向的cisRNA对.
- 构建一个ceRNA网络,揭示了参与病原体识别,激素信号和转录因子活性的基因的lncRNA和miRNA调节,这对植物免疫至关重要.
结论:
- 这项研究提供了米防突变中的lncRNAs,miRNAs和mRNAs的综合转录基因概况.
- 构建的跨向和 cis向网络,以及 ceRNA 网络,为 lncRNAs 的功能角色提供了洞察力.
- 这些发现强烈支持lncRNAs在米中OsRpp30介导的疾病耐药性的显著参与.
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
Global Regulatory Systems
29
Global regulatory systems in bacteria enable rapid and coordinated responses to environmental changes by integrating sensory inputs with gene expression, ensuring efficient adaptation to fluctuating conditions. Key global regulatory mechanisms include regulons, two-component systems, sigma factors, and secondary messengers.Regulons and Global RegulatorsA regulon is a collection of genes and operons controlled by a common global regulator. These regulators enable bacteria to prioritize resource...
29
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
Experimental RNAi
6.1K
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...
6.1K
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
Translational Regulation
28
Translational regulation in prokaryotes ensures efficient protein synthesis by controlling ribosome access to mRNA. This regulation is mediated by secondary RNA structures, including translational riboswitches, RNA thermometers, and small RNAs (sRNAs), which respond to intracellular and environmental signals to modulate gene expression.Translational RiboswitchesRiboswitches in the leader region of mRNAs can regulate translation by altering the accessibility of the Shine-Dalgarno (SD) sequence,...
28


