{"title":"Occurrence of the Slippery Sequence UUUAAAC in the RNA Genome 2 that generates the ORF1ab Protein of SARS-CoV-2","authors":"H. Geurdes","doi":"10.35248/2161-0517.20.9.198","DOIUrl":null,"url":null,"abstract":"In the present brief report we look into the slippery sequence TTTAAAC (in cDNA format) of the ORF1ab protein of SARS-CoV-2. We found a number of TTTAAAC sequences where only one is actively producing a shift-1. There are three other sequences exactly positioned in the read-through of mRNA as the aforementioned. They do not produce a-1 frameshift. There is one position where in addition a pseudoknot occurs but no frameshift. We ask if it is possible to enforce or prevent shifts in TTTAAAC to destroy the ORF1ab derived proteins such as RNA-dependent RNA polymerase and/or 2’-O-ribose methyltransferase. Finally an mRNA polymer repressor of the one single effective frameshift is proposed for further research into a medicinal treatment. Perhaps that there are specific protein repressors.","PeriodicalId":91631,"journal":{"name":"Virology & mycology : infectious diseases","volume":"9 1","pages":"1-4"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virology & mycology : infectious diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/2161-0517.20.9.198","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In the present brief report we look into the slippery sequence TTTAAAC (in cDNA format) of the ORF1ab protein of SARS-CoV-2. We found a number of TTTAAAC sequences where only one is actively producing a shift-1. There are three other sequences exactly positioned in the read-through of mRNA as the aforementioned. They do not produce a-1 frameshift. There is one position where in addition a pseudoknot occurs but no frameshift. We ask if it is possible to enforce or prevent shifts in TTTAAAC to destroy the ORF1ab derived proteins such as RNA-dependent RNA polymerase and/or 2’-O-ribose methyltransferase. Finally an mRNA polymer repressor of the one single effective frameshift is proposed for further research into a medicinal treatment. Perhaps that there are specific protein repressors.