作者: Toni Gabaldon , Ester Saus , Uciel Chorostecki
DOI: 10.1101/2021.03.29.437547
关键词: Sequence (medicine) 、 Structural motif 、 Cellular functions 、 Computational biology 、 RNA 、 Genomic Stability 、 Protein secondary structure 、 Function (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.