Transcriptomic analysis of diplomonad parasites reveals a trans-spliced intron in a helicase gene in Giardia
The mechanisms by which DNA sequences are expressed is the central preoccupation of molecular genetics. Recently, ourselves and others reported that in the diplomonad protist , the coding regions of several mRNAs are produced by ligation of independent RNA species expressed from distinct genomic loc...
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Veröffentlicht in: | PeerJ (San Francisco, CA) CA), 2017-01, Vol.5, p.e2861-e2861, Article e2861 |
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Zusammenfassung: | The mechanisms by which DNA sequences are expressed is the central preoccupation of molecular genetics. Recently, ourselves and others reported that in the diplomonad protist
, the coding regions of several mRNAs are produced by ligation of independent RNA species expressed from distinct genomic loci. Such trans-splicing of introns was found to affect nearly as many genes in this organism as does classical cis-splicing of introns. These findings raised questions about the incidence of intron trans-splicing both across the
transcriptome and across diplomonad diversity in general, however a dearth of transcriptomic data at the time prohibited systematic study of these questions.
I leverage newly available transcriptomic data from
and the related diplomonad
to search for trans-spliced introns. My computational pipeline recovers all four previously reported trans-spliced introns in
, suggesting good sensitivity.
Scrutiny of thousands of potential cases revealed only a single additional trans-spliced intron in
, in the p68 helicase gene, and no cases in
. The p68 intron differs from the previously reported trans-spliced introns in its high degree of streamlining: the core features of
trans-spliced introns are closely packed together, revealing striking economy in the implementation of a seemingly inherently uneconomical molecular mechanism.
These results serve to circumscribe the role of trans-splicing in diplomonads both in terms of the number of genes effected and taxonomically. Future work should focus on the molecular mechanisms, evolutionary origins and phenotypic implications of this intriguing phenomenon. |
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ISSN: | 2167-8359 2167-8359 |
DOI: | 10.7717/peerj.2861 |