Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/115905
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dc.titleRegulation of mRNA 1 expression by the 5'-untranslated region (5'-UTR) of the coronavirus infectious bronchitis virus (IBV)
dc.contributor.authorLiu, D.X.
dc.contributor.authorXu, H.Y.
dc.contributor.authorLim, K.P.
dc.date.accessioned2014-12-12T07:33:57Z
dc.date.available2014-12-12T07:33:57Z
dc.date.issued1998
dc.identifier.citationLiu, D.X.,Xu, H.Y.,Lim, K.P. (1998). Regulation of mRNA 1 expression by the 5'-untranslated region (5'-UTR) of the coronavirus infectious bronchitis virus (IBV). Advances in Experimental Medicine and Biology 440 : 303-311. ScholarBank@NUS Repository.
dc.identifier.issn00652598
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/115905
dc.description.abstractIn this report, we show that expression of the coronavirus IBV mRNA1 is regulated by its 5'-UTR. Evidence presented demonstrates that the IBV sequence from nucleotide 1 to 1904 directs very inefficient synthesis of a product of approximately 43 kDa. Deletion of either the first 362 bp or the whole part of the 5'-UTR, however, dramatically increased the expression of the 43 kDa protein species. The mechanisms involved were investigated by two different approaches. Firstly, translation of the same construct in the presence of [3H]-leucine ruled out the possibility that initiation of small reading frames from non-AUG codons located in the 5'-UTR may compete with the authentic AUG initiation codon, and therefore inhibit the expression of ORF 1a. Secondly, expression and deletion analyses of a dicistronic construct showed that translation of the 43 kDa protein was initiated by ribosome internal entry mechanism. These studies suggest that a 'weak' ribosome internal entry signal is located in the 5'-UTR and is involved in the regulation of mRNA1 expression.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR AGROBIOLOGY
dc.description.sourcetitleAdvances in Experimental Medicine and Biology
dc.description.volume440
dc.description.page303-311
dc.description.codenAEMBA
dc.identifier.isiutNOT_IN_WOS
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