Evolutionary divergence of Firre localization and expression

Long noncoding RNAs (lncRNAs) are rapidly evolving and thus typically poorly conserved in their sequences. How these sequence differences affect the characteristics and potential functions of lncRNAs with shared synteny remains unclear. Here we show that the syntenically conserved lncRNA Firre displays distinct expression and localization patterns in human and mouse. Single molecule RNA FISH reveals that in a range of cell lines, mouse Firre (mFirre) is predominantly nuclear, while human FIRRE (hFIRRE) is distributed between the cytoplasm and nucleus. This localization pattern is maintained in human/mouse hybrid cells expressing both human and mouse Firre, implying that the localization of the lncRNA is species autonomous. We find that the majority of hFIRRE transcripts in the cytoplasm are comprised of isoforms that are enriched in RRD repeats. We furthermore determine that in various tissues, mFirre is more highly expressed than its human counterpart. Our data illustrate that the rapid evolution of syntenic lncRNAs can lead to variations in lncRNA localization and abundance, which in turn may result in disparate lncRNA functions even in closely related species.

Automated summary

The research shows that the syntenically conserved lncRNA Firre displays distinct expression and localization patterns in humans and mice. Mouse Firre is predominantly located in the nucleus, while human FIRRE is distributed between the cytoplasm and nucleus. The localization of the lncRNA is believed to be species autonomous when expressed in human/mouse hybrid cells. The majority of hFIRRE transcripts in the cytoplasm contain isoforms enriched in RRD repeats, and mFirre is more highly expressed than its human counterpart in various tissues.