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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...
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Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
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From DNA to Protein

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The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
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Transfer RNA Synthesis02:36

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One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
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As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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Decoding codon usage in human papillomavirus type 59.

Xiaochun Tan1, Wenyi Zhou1, Shunyou Jing2

  • 1Department of Laboratory Medicine, The First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, 1882 South Central Road, Jiaxing, 314000, China.

Virus Genes
|March 4, 2025
PubMed
Summary

Human Papillomavirus Type 59 (HPV-59) exhibits mild codon usage bias, favoring A/T-ending codons and underrepresenting CpG sites. Natural selection and mutational pressure shape its codon usage, influencing vaccine development.

Keywords:
Codon usage biasHost adaptationHuman papillomavirus type 59Natural selectionRelative synonymous codon usage

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Area of Science:

  • Virology
  • Genomics
  • Molecular Biology

Background:

  • Human Papillomavirus Type 59 (HPV-59) is a high-risk HPV subtype associated with various cancers.
  • Understanding HPV-59 codon usage is crucial for viral behavior insights and vaccine optimization.
  • Codon usage patterns of HPV-59 remain largely underexplored.

Purpose of the Study:

  • To investigate the codon usage patterns of Human Papillomavirus Type 59 (HPV-59).
  • To determine the factors influencing HPV-59 codon usage bias.
  • To assess the evolutionary relationship between HPV-59 and its host's translational machinery for vaccine design.

Main Methods:

  • Analysis of HPV-59 genome sequences.
  • Application of codon usage bias metrics (e.g., Effective Number of Codons, Parity Rule 2).
  • Evaluation of mutational pressure and natural selection influences.
  • Assessment of host-virus translational compatibility using indices like CAI and RCSI.

Main Results:

  • HPV-59 displays a mild codon usage bias, with a preference for A/T-ending codons.
  • CpG dinucleotides are significantly underrepresented in the HPV-59 genome, potentially for immune evasion.
  • Both mutational pressure and natural selection shape codon usage, with natural selection being dominant.
  • HPV-59 codon usage shows moderate alignment with the human translational machinery.

Conclusions:

  • Codon usage in HPV-59 is shaped by a balance between mutational forces and natural selection.
  • The observed codon bias and CpG underrepresentation offer insights into HPV-59's biology and immune evasion strategies.
  • Findings provide a basis for developing more effective HPV-59 vaccines by considering viral codon usage and host compatibility.