The fragile X syndrome repeats form RNA hairpins that do not activate the interferon‐inducible protein kinase, PKR, but are cut by Dicer
V Handa, T Saha, K Usdin - Nucleic acids research, 2003 - academic.oup.com
V Handa, T Saha, K Usdin
Nucleic acids research, 2003•academic.oup.comWe show here that under physiologically reasonable conditions, CGG repeats in RNA
readily form hairpins. In contrast to its DNA counterpart that forms a complex mixture of
hairpins and tetraplexes, r (CGG) 22 forms a single stable hairpin with no evidence for any
other folded structure even at low pH. RNA with the sequence (CGG) 9AGG (CGG) 12AGG
(CGG) 97, found in a fragile X syndrome pre‐mutation allele, forms a number of different
hairpins. The most prominent hairpin forms in the 3′ part of the repeat and involves the 97 …
readily form hairpins. In contrast to its DNA counterpart that forms a complex mixture of
hairpins and tetraplexes, r (CGG) 22 forms a single stable hairpin with no evidence for any
other folded structure even at low pH. RNA with the sequence (CGG) 9AGG (CGG) 12AGG
(CGG) 97, found in a fragile X syndrome pre‐mutation allele, forms a number of different
hairpins. The most prominent hairpin forms in the 3′ part of the repeat and involves the 97 …
Abstract
We show here that under physiologically reasonable conditions, CGG repeats in RNA readily form hairpins. In contrast to its DNA counterpart that forms a complex mixture of hairpins and tetraplexes, r(CGG)22 forms a single stable hairpin with no evidence for any other folded structure even at low pH. RNA with the sequence (CGG)9AGG (CGG)12AGG(CGG)97, found in a fragile X syndrome pre‐mutation allele, forms a number of different hairpins. The most prominent hairpin forms in the 3′ part of the repeat and involves the 97 uninterrupted CGG repeats. In contrast to the CUG‐RNA hairpins formed by myotonic dystrophy type 1 repeats, we found no evidence that CGG‐RNA hairpins activate PKR, the interferon‐inducible protein kinase that is activated by a wide range of double‐stranded RNAs. However, we do show that the CGG‐RNA is digested, albeit inefficiently, by the human Dicer enzyme, a step central to the RNA interference effect on gene expression. These data provide clues to the basis of the toxic effect of CGG‐RNA that is thought to occur in fragile X pre‐mutation carriers. In addition, RNA hairpins may also account for the stalling of the 40S ribosomal subunit that is thought to contribute to the translation deficit in fragile X pre‐mutation and full mutation alleles.
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