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The evolution of lncRNA repertoires and expression patterns in tetrapods

GSE43520 Gallus gallus; Ornithorhynchus anatinus; Monodelphis domestica; Xenopus tropicalis; Macaca mulatta; Gorilla gorilla; Homo sapiens; Mus musculus Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing 55 samples Submitted 2014/01/19 Platform GPL13797Platform GPL16133Platform GPL15472Platform GPL13766Platform GPL13798Platform GPL15381Platform GPL9115Platform GPL13801Platform GPL10999Platform GPL13741Platform GPL17497Platform GPL11002Platform GPL11154Platform GPL13799Platform GPL13112
Summary
Only a minuscule fraction of long non-coding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into their functionality, but comparative analyses have been precluded by our ignorance of lncRNAs in non-model organisms. Here, we use RNA sequencing to identify lncRNAs in eleven tetrapod species and we present the first large-scale evolutionary study of lncRNA repertoires and expression patterns. We identify ~11,000 primate- specific lncRNA families, which show evidence for selective constraint during recent evolution, and ~2,400 highly conserved lncRNAs (including ~400 genes that likely originated more than 300 million years ago). We find that lncRNAs, in particular ancient ones, are generally actively regulated and may predominantly function in embryonic development. lncRNA X-inactivation patterns reveal an extremely female-biased monotreme-specific lncRNA, which may partially compensate X-dosage in this lineage. Most lncRNAs evolve rapidly in terms of sequence and expression levels, but global patterns like tissue specificities are often conserved. We compared expression patterns of homologous lncRNA and protein-coding families across tetrapods to reconstruct an evolutionarily conserved co-expression network. This network, which surprisingly contains many lncRNA hubs, suggests potential functions for lncRNAs in fundamental processes like spermatogenesis or synaptic transmission, but also in more specific mechanisms such as placenta growth suppression through miRNA production.
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Direct links to NCBI, no account and no request form: the whole study as GSE43520_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 55 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA186646 and SRA study SRP017959. Searching any of these in the dataset finder brings you back here.

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