Identification and characterization of a silent mutation in RNA binding domain of N protein coding gene from SARS-CoV-2.
Reza Zolfaghari EmamehMahyar EftekhariHassan NosratiJalal HeshmatniaReza FalakPublished in: BMC research notes (2021)
In the DNA sequence isolated from severe acute respiratory syndrome (SARS-CoV-2) in Iran, a coding sequence for the RNA binding domain of N protein was detected. The comparison of Chinese and Iranian DNA sequences displayed that a thymine (T) was mutated to cytosine (C), so "TTG" from China was changed to "CTG" in Iran. Both DNA sequences from Iran and China have been encoded for leucine. In addition, the second T in "CTG" in the DNA or uracil (U) in "CUG" in the RNA sequences from Iran can be mutated to another C by a missense mutation resulting from thymine DNA glycosylase (TDG) of human and base excision repair mechanism to produce "CCG" encoding for proline, which consequently may increase the affinity of the RNA binding domain of N protein to viral RNA and improve the transcription rate, pathogenicity, evasion from human immunity system, spreading in the human body, and risk of human-to-human transmission rate of SARS-CoV-2.
Keyphrases
- sars cov
- endothelial cells
- circulating tumor
- nucleic acid
- induced pluripotent stem cells
- single molecule
- cell free
- pluripotent stem cells
- binding protein
- gene expression
- autism spectrum disorder
- amino acid
- transcription factor
- escherichia coli
- protein protein
- pseudomonas aeruginosa
- dna damage
- intellectual disability
- small molecule
- biofilm formation
- wild type