血液转录组学分析提供了对SARS-CoV-2变种特异性免疫反应的见解
Markus Hoffmann1,2,3, Lina-Liv Willruth4, Alexander Dietrich4
1Data Science in Systems Biomedicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany. markus.hoffmann@nih.gov.
Scientific reports
|February 2, 2024
概括
大量RNA测序 (RNA-seq) 提供了一个强大的诊断工具,揭示了免疫细胞组成和B细胞/T细胞受体谱. 这种方法为免疫状态和疾病分类提供了宝贵的见解,即使每样本读数为1000万次.
科学领域:
- 基因组学就是基因组学.
- 免疫学 免疫学 免疫学
- 生物信息学是一种生物信息学.
背景情况:
- 大量RNA测序 (RNA-seq) 尽管具有潜力,但在临床实践中尚未得到充分利用.
- 目前的临床诊断依赖于全血细胞计 (CBC) 等方法,这些方法提供有限的分子洞察力.
研究的目的:
- 建立大量RNA-seq作为全面免疫分析的诊断工具.
- 评估RNA-seq用于评估免疫细胞组成,基因表达和B细胞/T细胞受体 (BCR/TCR) 谱.
- 为了确定可靠的诊断RNA-seq分析所需的最小测序深度.
主要方法:
- 对计算细胞类型解卷方法 (MCP计数器,xCell,EPIC,quanTIseq) 与CBC数据进行比较分析.
- 使用MiXCR和TRUST4识别和分析BCR/TCR序列,结合序列对齐和BLASTp.
- 对来自196名感染SARS-CoV-2变种的患者的大量RNA-seq数据的分析.
主要成果:
- RNA-seq提供了对免疫状况的见解,包括淋巴细胞枯竭和中性粒细胞水平在SARS-CoV-2变种中的变化.
- 分析BCR/TCR目录有助于对患者的疾病状况进行分类.
- 每个样本1000万次读取足以进行准确的诊断RNA-seq分析.
结论:
- 大量RNA-seq,使用计算解卷和BCR/TCR方法,可以补充CBC数据用于增强诊断.
- RNA-seq为免疫反应,疾病严重程度和病原体特异性免疫提供了深入的见解.
- 具有成本效益的RNA-seq分析 (千万读数/样本) 是可行的临床应用.
相关概念视频
Ribosome Profiling
3.5K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
3.5K
Single Nucleotide Polymorphisms-SNPs
15.1K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.1K
General Transcription Factors
5.3K
Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
5.3K
Leaky Scanning
5.1K
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...
5.1K


