缺陷的KERNEL 56在线粒体RNA编辑和玉米种子发育中的功能
Jie Zang1, Tengfei Zhang1,2, Zhaogui Zhang1
1State Key Laboratory of Plant Cell and Chromosome Engineering, Innovative Academy of Seed Design, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Plant physiology
|November 13, 2023
概括
一项新的研究确定了DEFECTIVE KERNEL 56 (DEK56),这是一种线粒体皮质重复 (PPR) 蛋白,对玉米种子发育至关重要. 它的功能障碍影响RNA编辑和拼接,揭示了内核形成的关键机制.
科学领域:
- 植物生物学 植物生物学
- 分子遗传学 分子遗传学
- 线粒体生物学 线粒体生物学
背景情况:
- 五蛋白重复 (PPR) 蛋白通过线粒体基因的转录后修饰来调节玉米核的发育.
- 在玉米种子发育中的PPR蛋白功能的精确机制尚未完全理解.
研究的目的:
- 描述DEK56在玉米种子发育中的功能.
- 阐明DEK56在线粒体基因调节和核形成中的作用背后的分子机制.
主要方法:
- 基于地图的克隆来识别DEK56基因.
- 在dek56突变体中分析RNA编辑和拼接效率.
- 蛋白质与蛋白质相互作用测试以确定相互作用伙伴.
主要成果:
- DEK56编码了线粒体E子组PPR蛋白,这对胚胎和内的发育至关重要.
- DEK56功能障碍改变了48个部位的RNA编辑,并降低了nad4内子的拼接效率.
- DEK56与由ZmMORFs和ZmGRP23.3促进的PPR动机,卷轴-卷轴和DYW域含有蛋白1 (PCW1) 相互作用.
结论:
- DEK56通过PPR介导的线粒体RNA处理在玉米种子发育中发挥着关键作用.
- 这些发现为线粒体基因调节中的PPR蛋白功能提供了一个工作模型.
- 这项研究提供了通过了解种子发育机制来改善玉米的见解.
相关概念视频
RNA Editing
9.0K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.0K
Nonsense-mediated mRNA Decay
10.6K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.6K
Nuclear Export of mRNA
7.7K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
7.7K
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
mRNA Stability and Gene Expression
5.6K
The structure and stability of mRNA molecules regulates gene expression, as mRNAs are a key step in the pathway from gene to protein. In eukaryotes, the half-life of mRNA varies from a few minutes up to several days. mRNA stability is essential in growth and development. The absence of the proteins regulating its stability, such as tristetraprolin in mice, can cause systemic issues, including bone marrow overgrowth, inflammation, and autoimmunity.
Cis-acting Elements involved in mRNA stability
Cis-acting Elements involved in mRNA stability
5.6K
Pre-mRNA Processing: Modification of pre-mRNA Ends
9.3K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
9.3K


