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Identification and Characterization of a Class of MALAT1-like Genomic Loci
Author(s) -
Bin Zhang,
Yuntao S. Mao,
Sarah D. Diermeier,
Iriovikova,
Eric P. Nawrocki,
Tom Jones,
Zsolt I. Lázár,
ChangShung Tung,
Weijun Luo,
Sean R. Eddy,
Karissa Y. Sanbonmatsu,
David L. Spector
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.05.006
Subject(s) - biology , piwi interacting rna , malat1 , genetics , rna , genome , gene , transfer rna , long non coding rna , non coding rna , transposable element , computational biology
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.

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