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Published on: May 19, 2019
The RIDL hypothesis: transposable elements as functional domains of long noncoding RNAs
1Centre for Genomic Regulation (CRG), 08003 Barcelona, Spain Universitat Pompeu Fabra (UPF), 08003 Barcelona, Spain Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), 08003 Barcelona, Spain.
Transposable elements (TEs) within long noncoding RNAs (lncRNAs) may function as Repeat Insertion Domains of LncRNAs (RIDLs). These TE-derived domains are crucial for lncRNA function and evolution.
Area of Science:
- Genomics
- Molecular Biology
- Evolutionary Biology
Background:
- Long noncoding RNAs (lncRNAs) are abundant in the genome and possess regulatory functions.
- The functional domains of lncRNAs are not well understood.
- Transposable elements (TEs) are mobile genetic sequences that contribute to genome evolution via exaptation.
Purpose of the Study:
- To propose that exonic TEs in lncRNAs function as essential RNA domains.
- To introduce the concept of Repeat Insertion Domains of LncRNAs (RIDLs).
- To suggest that TEs are repurposed as recognition sites for nucleic acids and proteins during lncRNA evolution.
Main Methods:
- Review of existing literature on lncRNAs and TEs.
- Analysis of experimentally defined RIDLs.
- Discussion of potential genomic screening strategies for RIDL discovery.
Main Results:
- TE-derived fragments within lncRNAs, termed RIDLs, have been experimentally identified.
- RIDLs function as RNA-, DNA-, and protein-binding domains.
- The exaptation of TEs provides a mechanism for lncRNA functional evolution.
Conclusions:
- The RIDL hypothesis offers a framework for understanding lncRNA functional evolution.
- TEs can be repurposed as functional domains within lncRNAs.
- Genomic maps of TEs may predict lncRNA function.
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