探索Codon使用模式和影响RanavirusDNA聚合酶基因的因素
1Department of Biology, Faculty of Arts and Sciences, Recep Tayyip Erdoğan University, Rize, Türkiye.
Journal of basic microbiology
|August 5, 2024
概括
拉纳病毒在其DNA聚合酶基因中表现出低编码子使用偏差,受突变压力和自然选择的影响. 这表明对这些病毒基因的强烈宿主适应性和进化选择压力.
科学领域:
- 病毒学 病毒学
- 生物信息学是一种生物信息学.
- 进化生物学 进化生物学
背景情况:
- 拉纳病毒对两动物和其他冷血脊椎动物构成重大全球威胁.
- 了解病毒基因演变对于管理拉纳病毒的出现至关重要.
研究的目的:
- 通过生物信息学研究Ranavirus DNA聚合酶基因中的子使用模式.
- 为了确定影响Ranavirus中codon使用偏差和宿主适应的因素.
主要方法:
- 对来自各种拉纳病毒的61个DNA聚合酶基因的分析.
- 评估相对同义使用率 (RSCU) 和适应指数 (CAI).
- 相关性分析包括核酸含量,有效编码数 (ENC) 和中性图.
主要成果:
- 拉纳病毒DNA聚合酶基因表现出低编码子使用偏差.
- 代码的使用主要是由自然选择驱动的,人们更喜欢以C或G结尾的代码.
- 分析表明,宿主适应能力强大,病毒基因的宿主选择压力很大.
结论:
- 自然选择是决定Ranavirus DNA聚合酶基因中代码的使用的主导力量.
- 拉纳病毒表现出对宿主的显著适应,这是由进化压力驱动的.
- 这些发现提供了对Ranavirus的进化和适应机制的见解.
相关概念视频
Bacterial RNA Polymerase
29.4K
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...
29.4K
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
Viral Mutations
32.2K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.2K
Eukaryotic RNA Polymerases
24.1K
RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
All three eukaryotic RNAPs require specific transcription factors, of which the...
24.1K
Gene Evolution - Fast or Slow?
7.1K
The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
In contrast, regions which code...
7.1K
Bacterial Transcription
28.1K
RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
28.1K


