Abstract

Long non-coding RNAs (lncRNAs) have important regulatory functions across eukarya. It is now clear that many of these functions are related to gene expression regulation through their capacity to recruit epigenetic modifiers and establish chromatin interactions. Several lncRNAs have been recently shown to participate in modulating chromatin within the spatial organization of the genome in the three-dimensional space of the nucleus. The identification of lncRNA candidates is challenging, as it is their functional characterization. Conservation signatures of lncRNAs are different from those of protein-coding genes, making identifying lncRNAs under selection a difficult task, and the homology between lncRNAs may not be readily apparent. Here, we review the evidence for these higher-order genome organization functions of lncRNAs in animals and the evolutionary signatures they display.

Highlights

  • The three-dimensional (3D) organization of DNA in the cell nucleus has become a significant subject of study, its influence on gene regulation

  • Chromosomes are subdivided into topologically associating domains (TADs) within which chromatin loops bring together regulatory elements and target loci separated in the linear genome (Dixon et al, 2012)

  • A more traditional example of positional conservation is the Long non-coding RNAs (lncRNAs) antisense to Igf2r RNA non-coding (Airn), required for paternal-specific silencing of imprinted genes in the insulin-like growth factor 2 (Igf2r) cluster (Sleutels et al, 2002)

Read more

Summary

Introduction

The three-dimensional (3D) organization of DNA in the cell nucleus has become a significant subject of study, its influence on gene regulation. The conservation signals in lncRNAs can differ from those typically found in protein-coding genes (Diederichs, 2014; Ulitsky, 2016). It is more common for lncRNAs to have short conserved motifs or domains that are important for their association with DNA or proteins that regulate chromatin conformation.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call