Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Feb 17:10:47.
doi: 10.1186/1471-2148-10-47.

Evolutionary dynamics of U12-type spliceosomal introns

Affiliations

Evolutionary dynamics of U12-type spliceosomal introns

Chiao-Feng Lin et al. BMC Evol Biol. .

Abstract

Background: Many multicellular eukaryotes have two types of spliceosomes for the removal of introns from messenger RNA precursors. The major (U2) spliceosome processes the vast majority of introns, referred to as U2-type introns, while the minor (U12) spliceosome removes a small fraction (less than 0.5%) of introns, referred to as U12-type introns. U12-type introns have distinct sequence elements and usually occur together in genes with U2-type introns. A phylogenetic distribution of U12-type introns shows that the minor splicing pathway appeared very early in eukaryotic evolution and has been lost repeatedly.

Results: We have investigated the evolution of U12-type introns among eighteen metazoan genomes by analyzing orthologous U12-type intron clusters. Examination of gain, loss, and type switching shows that intron type is remarkably conserved among vertebrates. Among 180 intron clusters, only eight show intron loss in any vertebrate species and only five show conversion between the U12 and the U2-type. Although there are only nineteen U12-type introns in Drosophila melanogaster, we found one case of U2 to U12-type conversion, apparently mediated by the activation of cryptic U12 splice sites early in the dipteran lineage. Overall, loss of U12-type introns is more common than conversion to U2-type and the U12 to U2 conversion occurs more frequently among introns of the GT-AG subtype than among introns of the AT-AC subtype. We also found support for natural U12-type introns with non-canonical terminal dinucleotides (CT-AC, GG-AG, and GA-AG) that have not been previously reported.

Conclusions: Although complete loss of the U12-type spliceosome has occurred repeatedly, U12 introns are extremely stable in some taxa, including eutheria. Loss of U12 introns or the genes containing them is more common than conversion to the U2-type. The degeneracy of U12-type terminal dinucleotides among natural U12-type introns is higher than previously thought.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Graphic depiction of the status of 442 human U12 intron clusters in A) Three eutheria, B) Seven vertebrates, C) Drosphila melanogaster, and D) Ciona intestinalis. The status of each intron is described as U12 in the comparison species, or in all comparison species (blue), at least one ambiguous intron in the comparison species or all comparison species (red), U2 in the comparison species or at least one of the several comparison species (yellow), missing intron (green), or missing gene - no orthologous gene detectable (violet).

Similar articles

Cited by

References

    1. Sharp PA. Split genes and RNA splicing. Cell. 1994;77:805–815. doi: 10.1016/0092-8674(94)90130-9. - DOI - PubMed
    1. Patel AA, Steitz JA. Splicing double: insights from the second spliceosome. Nature Rev Mol Cell Biol. 2003;4:960. doi: 10.1038/nrm1259. - DOI - PubMed
    1. Will CL, Luhrmann R. Splicing of a rare class of introns by the U12-dependent spliceosome. Biol Chem. 2005;386:713–724. doi: 10.1515/BC.2005.084. - DOI - PubMed
    1. Berget SM, Moore C, Sharp PA. Spliced segments at the 5' terminus of adenovirus 2 late mRNA. Proc Natl Acad Sci USA. 1977;74:3171–3175. doi: 10.1073/pnas.74.8.3171. - DOI - PMC - PubMed
    1. Breathnach R, Chambon P. Organization and expression of eucaryotic split genes coding for proteins. Annual Review of Biochemistry. 1981;50:349–383. doi: 10.1146/annurev.bi.50.070181.002025. - DOI - PubMed

Publication types