The <
i>
MALAT1<
/i>
(Metastasis-Associated Lung Adenocarcinoma Transcript 1) gene encodes a noncoding RNA that is processed into a long nuclear retained transcript (<
i>
MALAT1<
/i>
) 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 <
i>
MALAT1<
/i>
3' end triple-helix structure and its immediate downstream tRNA-like structure, including 44 in the green lizard <
i>
Anolis carolinensis<
/i>
. Structural and computational analyses revealed a co-occurrence of components of the 3' end module. <
i>
MALAT1<
/i>
-like genes in <
i>
Anolis carolinensis<
/i>
are highly expressed in adult testis, thus we named them testis-abundant long noncoding RNAs (tancRNAs). <
i>
MALAT1<
/i>
-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. Furthermore, 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.