早期宿主-病毒RNA相互作用揭示了SPEN驱动的m6规范作为赫尼帕病毒感染的主要决定因素
bioRxiv : the preprint server for biology
|December 3, 2025
概括
黑尼帕病毒感染依赖于宿主蛋白质,如SPEN,RBM15和RBM15B. 削弱SPEN会破坏RNA甲基化,阻碍病毒复制并揭示关键宿主依赖.
科学领域:
- 病毒学 病毒学
- 分子生物学分子生物学
- 宿主-病原体相互作用
背景情况:
- 河尼帕病毒是极具致命性的BSL-4病原体,其病原体性尚不清楚.
- 早期的病毒RNA和宿主RNA结合蛋白相互作用对于RNA病毒感染结果至关重要.
研究的目的:
- 在感染初期识别与黑尼帕病毒RNA相互作用的宿主蛋白.
- 阐明这些宿主因子在海尼帕病毒病原发生中的作用.
主要方法:
- 病毒交叉链接和固相净化 (VIR-CLASP) 用于在感染后的第一个小时内捕获与黑尼帕病毒RNA结合的宿主蛋白质.
- 使用直接RNA测序来分析RNA的修饰.
主要成果:
- 建立了第一个henipavirus RNA-宿主蛋白互动组,识别了与病毒RNA相关的146种人类蛋白质.
- 确定了SPEN,RBM15和RBM15B作为促进尼病毒感染的关键宿主因素.
- SPEN 枯竭导致广泛的RNA 低甲基化,特别是影响病毒RNA依赖的RNA聚合酶 (L) mRNA转录.
结论:
- 黑尼帕病毒感染在最早的阶段表现出对特定RNA结合蛋白的关键宿主依赖.
- 通过调节RNA甲基化,SPEN家族蛋白质在促进海尼帕病毒感染方面发挥了以前未知的作用.
相关概念视频
Viruses with RNA Genomes
751
RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
751
Leaky Scanning
5.6K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.6K
Size and Structure of Viral Genomes
626
Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
626
Retrovirus Life Cycles
49.2K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
49.2K
siRNA - Small Interfering RNAs
18.3K
Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
18.3K
RNA Interference
27.7K
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...
27.7K


