Minor spliceosome
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The minor spliceosome is a ribonucleoprotein complex that catalyses the removal (splicing) of an atypical class of spliceosomal introns (U12-type) from eukaryotic messenger RNAs in plant, insects, vertebrates and some fungi (Rhizopus oryzae). This process is called noncanonical splicing, as opposed to U2-dependent canonical splicing. U12-type introns represent less than 1% of all introns in human cells. However they are found in genes performing essential cellular functions.
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[edit] Early evidences
A notable feature of eukaryotic nuclear pre mRNA introns is the relatively high level of conservation of the primary sequences of 5’ and 3’ splice sites over a great range of organisms.
Since 1989 till 1991, several groups reported four independent examples of introns with a splice site that differed from the common intron:
- Cartilage matrix protein (CMP/MATN1) gene in human and chicken
- Proliferating cell nucleolar protein P120 (NOL1) gene in human
- mouse Rep3 gene, presumably involved in DNA repair
- Drosophila prospero gene that encodes for a homeobox protein
In 1991 by comparing the intron sequences of P120 and CMP genes, IJ Jackson reported the existence of ATATCC (5') and pypyCAC (3') splice sites in these introns. The finding indicated a possible novel splicing mechanism.
In 1994, S.L. Hall and R.A Padgett compared the primary sequence of all reports on the four genes mentioned above. The results suggested a new type of introns with ATATCCTT 5’ splice site and YCCAC 3’ splice site and an almost invariant TCCTTAAC near the 3’ end of the introns (so called 3’ upstream element). A search for small nuclear RNA sequences that are complementary to these splice sites, suggested U12 snRNA (matches 3’ sequence) and U11 snRNA (matches 5’sequence) as being putative factors involved in splicing of this new type of introns.
In all these four genes, the pre-mRNA contains other introns whose sequences conform to those of major class introns. Neither the size nor the position of the AT–AC intron within the host gene is conserved.
In 1996, Woan-Yuh Tarn and Joan A. Steitz described an in vitro system that splices a pre-mRNA substrate containing an AT–AC intron derived from the human P120 gene. Psoralen cross-linking confirms the base-pairing interaction predicted by Hall and Padgett between the branch site of the pre-mRNA substrate and U12 RNA. Native gel electrophoresis reveals that U11, U12, and U5 snRNPs assemble onto the P120 pre-mRNA to form splicing complexes.
[edit] Structure of U12-type introns and minor spliceosome
Athough originally referred to as ATAC introns, U12-type introns have GT-AG 5’ and 3’slice sites while some U2-type introns have AT-AC at their 5’ and 3’ ends.
The main determinants for distinguishing U2- and U12-type introns are 5’ splice site and branch site sequences.
Minor spliceosome consists of U11, U12, U4atac, and U6atac, together with U5 and a unknown number of non-snRNP proteins. The U11, U12 and U4atac/U6atac snRNPs are functional analogs of the U1, U2 and U4/U6 snRNPs in major spliceosome. [1] [2][3][4] [5] Although the minor U4atac and U6atac snRNAs are functional analogs of U4 and U6, respectively, they share only limited sequence homology (ca. 40%). Furthermore, the sequence of U11 in comparison with U1, as well as U12 compared with U2, are completely unrelated. Despite this fact, the minor U11, U12, U4atac and U6atac snRNAs can be folded into structures similar to U1, U2, U4 and U6, respectively.[6]
[edit] Evolution of minor spliceosome
Like major spliceosome, minor spliceosome had an early origin: several of its characteristic constituents are present in representative organisms from all eukaryotic supergroups for which there is any substantial genome sequence information. In addition, functionally important sequence elements contained within U12-type introns and snRNAs are highly conserved during evolution.
[edit] References
Review papers:
- Will CL, Luhrmann R. Biol Chem. 2005 Aug;386(8):713-24. Review.
Classic papers:
- S.L. Hall and R.A. Padgett, J. Mol. Biol. 239 (1994), pp. 357–365.
- I.J. Jackson, Nucleic Acids Research Volume 19, Issue 14 , July 25, 1991, Pages 3795-3798
- Woan-Yuh Tarn and Joan A. Steitz , Cell, Volume 84, Issue 5 , 8 March 1996, Pages 801-811
- Russell AG, Charette JM, Spencer DF, Gray MW. Nature. 2006 Oct 19;443(7113):863-6.
Other references:
- ^ Hall, S.L. and Padgett, R.A. (1996). Science 271, 1716–1718.
- ^ Tarn, W.Y. and Steitz, J.A. (1996b) Cell 84, 801–811.
- ^ Kolossova, I. and Padgett, R.A. (1997) RNA 3, 227–233
- ^ Yu, Y.T. and Steitz, J.A. (1997) Proc. Natl. Acad. Sci. USA 94, 6030–6035.
- ^ Incorvaia, R. and Padgett, R.A. (1998) RNA 4, 709–718.
- ^ Tarn, W.Y. and Steitz, J.A. (1996a) Science 273, 1824–1832.
