Project report

 

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Abstract

Recent works suggest that readthrough of stop codons can be one of the translation regulation controls, but its mechanism is still unclear especially in eukaryotes. From the latest study, we found that there may be several species-wide sequence characteristics in the 3' untranslated region (3fUTR) of readthrough genes, even though the factors or mechanisms to induce the event are different. Therefore, in this study, we hypothesized that 3'UTR of these readthrough genes have specific codon preferences similar to CDS comparing to those of regular genes. We examined CDS, 3'UTR of regular genes, and 3'UTR of known readthrough genes, and found that CDS and 3'UTR of regular genes have difference in codon preferences. However, many 3'UTR sequences of known readthrough genes had similarity to CDS, not to 3'UTR of regular genes. These results suggest that 3'UTR sequences which are synthesized by readthrough event use more optimal codons which are highly efficient for translation than the other regular genes whose 3'UTR are usually untranslated. Especially, codons whose 3rd position are Cytosine and code polar but uncharged amino acids such as ACC(Threonine), GGC(Glycine), and AGC(Serine) were well observed, suggesting the chemical specificity in conformation or binding to ribosome in readthrough event. These specific sequence characteristics in 3fUTR of readthrough genes may be widely preserved among many species, and the identification of these characteristics could be one of the important studies to understand stop codon readthrough.

 

Details are written in my master thesis