Pre-mRNA structures forming circular RNAs
Circular RNAs are a recently discovered class of RNAs formed by covalently linking the 5' and 3' end of an RNA. Pre-mRNAs generate circular RNAs through a back-splicing mechanism. Whereas in linear splicing a 5' splice site is connected to a downstream 3' splice site, in back-spl...
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Veröffentlicht in: | Biochimica et biophysica acta. Gene regulatory mechanisms 2019-11, Vol.1862 (11-12), p.194410-194410, Article 194410 |
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Sprache: | eng |
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Zusammenfassung: | Circular RNAs are a recently discovered class of RNAs formed by covalently linking the 5' and 3' end of an RNA. Pre-mRNAs generate circular RNAs through a back-splicing mechanism. Whereas in linear splicing a 5' splice site is connected to a downstream 3' splice site, in back-splicing the 5' splice site is connected to an upstream 3' splice site. Both mechanisms use the spliceosome for catalysis. For back-splicing to occur, the back-splice sites must frequently be brought into close proximity, which is achieved through the formation of secondary structures in the pre-mRNA. In general, these pre-mRNA structures are formed by RNA base pairing between complementary sequences flanking the back-splicing sites. Proteins can abolish these RNA structures through binding to one of the complementary strands. However, proteins can also promote back-splicing without strong RNA structures through multimerization after binding to intronic regions flanking circular exons. In humans, Alu-elements comprising around 11% of the human genome are the best-characterized elements generating structures promoting circular RNA formation. Thus, intronic pre-mRNA structures contribute to the formation of circular RNAs.
•Circular RNAs are an emerging class of RNAs•The formation of circular RNAs is promoted by double stranded regions in the pre-mRNA•RNA modifying enzymes, helicases and splicing regulators impact double stranded region formation•Primate-specific Alu elements and deep intronic mutations possibly act through circular RNAs |
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ISSN: | 1874-9399 1876-4320 |
DOI: | 10.1016/j.bbagrm.2019.194410 |