杰罗尼莫:在广泛的进化背景下系统地检索结构RNA的工具
Agata M Kilar1,2, Petr Fajkus1,3, Jiří Fajkus1,2,3
1Mendel Centre for Plant Genomics and Proteomics, CEITEC Masaryk University, Brno CZ-62500, Czech Republic.
GigaScience
|October 17, 2023
概括
鉴定非编码RNA (ncRNA) 同类因序列保存低而具有挑战性. 杰罗尼莫为跨基因组的进化ncRNA搜索提供了一个自动化解决方案,帮助进化模式调查.
科学领域:
- 生物信息学是一种生物信息学.
- 基因组学就是基因组学.
- 分子生物学分子生物学
背景情况:
- 非编码RNAs (ncRNAs) 往往缺乏序列保存,使同类鉴定复杂化.
- 保存的结构特征,而不是序列,是识别进化上遥远的ncRNAs的关键.
- 像Infernal这样的现有工具需要高级生物信息技术技能,而RNAcentral在全基因组搜索方面存在局限性.
研究的目的:
- 介绍GERONIMO,这是一个用于大规模,进化性ncRNA同类物搜索的自动化工具.
- 提供对不同生物和基因组的ncRNA进化进行用户友好的分析.
主要方法:
- 使用Snakemake工作流程管理系统开发GERONIMO.
- 自动化,全基因组的进化搜索ncRNA同类物.
- 纳入分类学上下文,可视化和基因组区域分析.
主要成果:
- 杰罗尼莫能够在数百个基因组中实现自动化,全面的进化搜索.
- 结果包括分类学上下文,摘要表和可视化以提高可用性.
- 围绕同类物体的基因组区域用于促进因子和基因对线性分析.
结论:
- 杰罗尼莫是一个强大的工具,用于识别跨多种分类群的ncRNA同类.
- 有助于研究功能显著的ncRNAs的进化模式.
- 克服了以前大规模ncRNA进化分析方法的局限性.
相关概念视频
RNA-seq
10.0K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.0K
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
RACE - Rapid Amplification of cDNA Ends
6.4K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
6.4K
Bacterial RNA Polymerase
29.6K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
29.6K
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
Genomic DNA in Eukaryotes
47.0K
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
47.0K


