Abstract

Advances in RNA sequencing technologies have led to the surprising discovery that a vast number of transcripts emanate from regions of the genome that are not part of coding genes. Although some of the smaller ncRNAs such as microRNAs have well-characterized functions, the majority of long ncRNA (lncRNA) functions remain poorly understood. Understanding the significance of lncRNAs is an important challenge facing biology today. A powerful approach to uncovering the function of lncRNAs is to explore temporal and spatial expression profiling. This may be particularly useful for classes of lncRNAs that have developmentally important roles as the expression of such lncRNAs will be expected to be both spatially and temporally regulated during development. Here, we take advantage of our ultra-high frequency (temporal) sampling of Xenopus embryos to analyze gene expression trajectories of lncRNA transcripts over the first 3 days of development. We computationally identify 5689 potential single- and multi-exon lncRNAs. These lncRNAs demonstrate clear dynamic expression patterns. A subset of them displays highly correlative temporal expression profiles with respect to those of the neighboring genes. We also identified spatially localized lncRNAs in the gastrula stage embryo. These results suggest that lncRNAs have regulatory roles during early embryonic development.

Highlights

  • X-chromosome (Brown et al, 1991; Gendrel and Heard, 2014)

  • We focused on identifying only intergenic long ncRNA (lncRNA) that do not show overlap with coding genes

  • Lowering the threshold will exponentially increase the number of open reading frame (ORF) identified, and will lead to the exclusion of many genuine lncRNAs

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Summary

Introduction

X-chromosome (Brown et al, 1991; Gendrel and Heard, 2014). H19 brings repressive histone marks to the differentially methylated regions of target genes (Bartolomei et al, 1991). A challenge in identifying lncRNAs is their general lack of sequence conservation across species and many lncRNA genes appear to lack orthologs across different species based on nucleotide sequence similarity. This led to the notion that lncRNA genes do not have the same evolutionary constraints as those of proteincoding genes and the conservation of lncRNAs is inherent in the folded structure (e.g., secondary and tertiary structures), instead of at the primary nucleotide sequence level (Johnsson et al, 2014).

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