| Literature DB >> 28538188 |
Bin Zhang1, Yuntao S Mao2, Sarah D Diermeier2, Irina V Novikova3, Eric P Nawrocki4, Tom A Jones5, Zsolt Lazar2, Chang-Shung Tung6, Weijun Luo7, Sean R Eddy5, Karissa Y Sanbonmatsu6, David L Spector8.
Abstract
The MALAT1 (Metastasis-Associated Lung Adenocarcinoma Transcript 1) gene encodes a noncoding RNA that is processed into a long nuclear retained transcript (MALAT1) and a small cytoplasmic tRNA-like transcript (mascRNA). Using an RNA sequence- and structure-based covariance model, we identified more than 130 genomic loci in vertebrate genomes containing the MALAT1 3' end triple-helix structure and its immediate downstream tRNA-like structure, including 44 in the green lizard Anolis carolinensis. Structural and computational analyses revealed a co-occurrence of components of the 3' end module. MALAT1-like genes in Anolis carolinensis are highly expressed in adult testis, thus we named them testis-abundant long noncoding RNAs (tancRNAs). MALAT1-like loci also produce multiple small RNA species, including PIWI-interacting RNAs (piRNAs), from the antisense strand. The 3' ends of tancRNAs serve as potential targets for the PIWI-piRNA complex. Thus, we have identified an evolutionarily conserved class of long noncoding RNAs (lncRNAs) with similar structural constraints, post-transcriptional processing, and subcellular localization and a distinct function in spermatocytes.Entities:
Keywords: Anolis carolinesis; MALAT1; PIWI; evolution; lizard; long noncoding RNA; piRNA; tRNA-like; testis; triple helix
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Year: 2017 PMID: 28538188 PMCID: PMC5505346 DOI: 10.1016/j.celrep.2017.05.006
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423