4.8 Article

5'-UTR G-quadruplex structures acting as translational repressors

期刊

NUCLEIC ACIDS RESEARCH
卷 38, 期 20, 页码 7022-7036

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gkq557

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资金

  1. Canadian Institutes of Health Research (CIHR) [MOP-44022, PRG-80169]
  2. Universite de Sherbrooke
  3. Fonds de Recherche en Sante du Quebec (FRSQ)

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Given that greater than 90% of the human genome is expressed, it is logical to assume that post-transcriptional regulatory mechanisms must be the primary means of controlling the flow of information from mRNA to protein. This report describes a robust approach that includes in silico, in vitro and in cellulo experiments permitting an in-depth evaluation of the impact of G-quadruplexes as translational repressors. Sequences including potential G-quadruplexes were selected within nine distinct genes encoding proteins involved in various biological processes. Their abilities to fold into G-quadruplex structures in vitro were evaluated using circular dichroism, thermal denaturation and the novel use of in-line probing. Six sequences were observed to fold into G-quadruplex structures in vitro, all of which exhibited translational inhibition in cellulo when linked to a reporter gene. Sequence analysis, direct mutagenesis and subsequent experiments were performed in order to define the rules governing the folding of G-quadruplexes. In addition, the impact of single-nucleotide polymorphism was shown to be important in the formation of G-quadruplexes located within the 5'-untranslated region of an mRNA. In light of these results, clearly the 5'-UTR G-quadruplexes represent a class of translational repressors that is broadly distributed in the cell.

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