Structural characterization of NORAD reveals a stabilizing role of spacers and two new repeat units.

作者: Toni Gabaldon , Ester Saus , Uciel Chorostecki

DOI: 10.1101/2021.03.29.437547

关键词: Sequence (medicine)Structural motifCellular functionsComputational biologyRNAGenomic StabilityProtein secondary structureFunction (biology)Biology

摘要: Long non-coding RNAs (IncRNAs) can perform a variety of key cellular functions by interacting with proteins and other RNAs. Recent studies have shown that the function IncRNAS are largely mediated their structures. However, our structural knowledge for most is limited to sequence-based computational predictions. Non-coding RNA activated DNA damage (NORAD) an atypical IncRNA due its abundant expression high sequence conservation. NORAD regulates genomic stability microRNAs. Previous characterization has identified modular organization composed several repeat units (NRUs). These comprise protein-binding elements separated regular spacers unknown function. Here, we experimentally determine first time secondary structure using nextPARS approach. Our results suggest spacer regions provide NRUs. Furthermore, uncover two previously-unreported NRUs, core motifs conserved across Overall, these findings will help elucidate evolution NORAD.

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