کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2039718 | 1073076 | 2016 | 11 صفحه PDF | دانلود رایگان |

• Bioinformatics reveals ∼200 distinct ENEs in transposable elements of lower eukaryotes
• Tested ENEs stabilize a reporter mRNA in human cells
• The ENEs are predicted to form stacks of two to five U⋅A-U triples
• In hAT DNA transposons, intronless transposase genes accumulate ENEs
SummaryThe ENE (element for nuclear expression) is a cis-acting RNA structure that protects viral or cellular noncoding RNAs (ncRNAs) from nuclear decay through triple-helix formation with the poly(A) tail or 3′-terminal A-rich tract. We expanded the roster of nine known ENEs by bioinformatic identification of ∼200 distinct ENEs that reside in transposable elements (TEs) of numerous non-metazoan and one fish species and in four Dicistrovirus genomes. Despite variation within the ENE core, none of the predicted triple-helical stacks exceeds five base triples. Increased accumulation of reporter transcripts in human cells demonstrated functionality for representative ENEs. Location close to the poly(A) tail argues that ENEs are active in TE transcripts. Their presence in intronless, but not intron-containing, hAT transposase genes supports the idea that TEs acquired ENEs to counteract the RNA-destabilizing effects of intron loss, a potential evolutionary consequence of TE horizontal transfer in organisms that couple RNA silencing to splicing deficits.
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Journal: - Volume 15, Issue 6, 10 May 2016, Pages 1266–1276