Nature Structural & Molecular BiologyMolecular BiologyPeer-reviewed journal article
An Atypical RNA Quadruplex Marks RNAs as Vectors for Gene Silencing
Saeed RoschdiiD, Jenny Jiacheng YaniD, Yuichiro NomuraiD, Cristian A. EscobariD, Riley J. PeterseniD, C.A. BingmaniD, Marco TonelliiD, Rahul VivekiD, Eric MontemayoriD, Marvin WickensiD, Scott G. KennedyiD, Samuel E. ButcheriD
Abstract
The addition of poly(UG) ("pUG") repeats to 3' termini of mRNAs drives gene silencing and trans-generational epigenetic inheritance in the metazoan C. elegans.1 pUG tails promote silencing by recruiting an RNA-dependent RNA Polymerase (RdRP) that synthesizes small interfering (si)RNAs.1 Here we show that active pUG tails require a minimum of 11.5 repeats and adopt a quadruplex (G4)2 structure we term the pUG fold. The pUG fold differs from known G4s in that it has a left-handed backbone similar to Z-RNA3,4, no consecutive guanosines in its sequence, and three G quartets and one U quartet stacked non-sequentially. Its biological importance is emphasized by our observations that porphyrin molecules bind to the pUG fold and inhibit both gene silencing and binding of RdRP. Moreover, specific N7-deaza RNA substitutions that do not adopt the pUG fold neither bind RdRP nor induce RNA silencing. These data define the pUG fold as a previously unrecognized RNA secondary structure motif that drives gene silencing. The pUG fold can also form internally within larger RNA molecules. Approximately 20,000 pUG-fold sequences are found in non-coding regions of human RNAs, suggesting the fold likely has biological roles beyond gene silencing.
- organism: C. elegans
- organism: human
- assay: multiome
- assay: DNA methylation
- assay: proteomics
- research focus: gene regulatory network inference
- research focus: sequence-to-function modeling
- research focus: database / resource
- approach: statistical model
- approach: experimental assay
- Citations
- 66
- FWCI
- 4.24
- Field percentile
- top 4%
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