Outron

An outron is a nucleotide sequence at the 5' end of the primary transcript of a gene that is removed by a special form of RNA splicing during maturation of the final RNA product.[1] Whereas intron sequences are located inside the gene, outron sequences lie outside the gene.[2]

Characteristics

The outron is an intron-like sequence possessing similar characteristics such as the G+C content[3] and a splice acceptor site that is the signal for trans-splicing.[4][5] Such a trans-splice site is essentially defined as an acceptor (3') splice site without an upstream donor (5') splice site.

In eukaryotes such as euglenozoans, dinoflagellates, sponges, nematodes, cnidarians, ctenophores, flatworms, crustaceans, chaetognaths, rotifers, and tunicates, the length of spliced leader (SL) outrons range from 30 to 102 nucleotides (nt), with the SL exon length ranging from 16 to 51 nt, and the full SL RNA length ranging from 46 to 141 nt.[3]

Processing

In standard cis-splicing, the donor splice site in upstream position is required together with an acceptor site located on downstream position on the same pre-RNA molecule. By contrast, the SL trans-splicing relies on a 3' acceptor splice site on the outron, and a 5' donor splice site (GU dinucleotide) located on a separate RNA molecule, the SL RNA.[3] Moreover, the outron of the premature mRNA contains a branchpoint adenosine — followed by a downstream polypyrimidine tract — which interacts with the intron-like portion of the SL RNA to form a 'Y' branched byproduct, reminiscent of the lasso structure formed during intron splicing. Nuclear machinery then resolves this 'Y' branching structure by trans-splicing the SL RNA sequence to the 3′ trans-splice acceptor site (AG dinucleotide) of the pre-mRNA.[2]

When outrons are processed, the SL exon is trans-spliced to distinct, unpaired, downstream acceptor sites adjacent to each open reading frame of the polycistronic pre-mRNA, leading to distinct mature capped transcripts. [6][7][8]

gollark: Yes.
gollark: BRF is evil and should be discouraged.
gollark: SI prefixes.
gollark: <@148963262535434240> 1.5GRF, you mean.
gollark: You can tell, from the lava where the fusion core was, and the lack of electromagnets.

See also

References
  1. Conrad, Richard; Fen Liou, Ruey; Blumenthal, Thomas (1993-02-25). "Functional analysis of a C. elegans trans-splice acceptor". Nucleic Acids Research. 21 (4): 913–919. doi:10.1093/nar/21.4.913. ISSN 0305-1048. PMC 309224. PMID 8451190.
  2. Stover, Nicholas A.; Kaye, Michelle S.; Cavalcanti, Andre R. O. (2006-01-10). "Spliced leader trans-splicing". Current Biology. 16 (1): R8–R9. doi:10.1016/j.cub.2005.12.019. ISSN 0960-9822. PMID 16401417.
  3. Lasda, Erika L.; Blumenthal, Thomas (2011-05-01). "Trans-splicing". Wiley Interdisciplinary Reviews: RNA. 2 (3): 417–434. doi:10.1002/wrna.71. PMID 21957027.
  4. "Oxford reference — Outron". Retrieved 26 September 2019.
  5. "The MISO Sequence Ontology Browser — Outron (SO:0001475)". Retrieved 26 September 2019.
  6. Clayton, Christine E. (2002-04-15). "Life without transcriptional control? From fly to man and back again". The EMBO Journal. 21 (8): 1881–1888. doi:10.1093/emboj/21.8.1881. ISSN 1460-2075. PMC 125970. PMID 11953307.
  7. Blumenthal, Thomas; Gleason, Kathy Seggerson (February 2003). "Caenorhabditis elegans operons: form and function". Nature Reviews Genetics. 4 (2): 110–118. doi:10.1038/nrg995. ISSN 1471-0056. PMID 12560808.
  8. Lei Q, Li C, Zuo Z, Huang C, Cheng H, Zhou R (March 2016). "Evolutionary Insights into RNA trans-Splicing in Vertebrates". Genome Biology and Evolution. 8 (3): 562–77. doi:10.1093/gbe/evw025. PMC 4824033. PMID 26966239.
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