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U4 spliceosomal RNA

 
Wikipedia: U4 spliceosomal RNA
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U4 spliceosomal RNA
U4
Type: Gene;snRNA;splicing;
2° structure: Published; PubMed; Griffiths-Jones SR
Seed alignment: Zwieb C, The uRNA database, PubMed
Avg length: 138.20 nucleotides
Avg identity: 54.00%
A 3D representation of a fragment of a U4 snRNA. The crystal structure of the spliceosomal 15.5KD protein bound to a U4 snRNA fragment.[1]

The U4 small nuclear Ribo-Nucleic Acid (U4 snRNA) is a non-coding RNA component of the major or U2-dependent spliceosome – a eukaryotic molecular machine involved in the splicing of pre-messenger RNA (pre-mRNA). It forms a duplex with U6, and with each splicing round, it is displaced from the U6 snRNA (and the spliceosome) in an ATP-dependent manner, allowing U6 to re-fold and create the active site for splicing catalysis. A recycling process involving protein Brr2 releases U4 from U6, while protein Prp24 re-anneals U4 and U6. The crystal structure of a 5′ stem-loop of U4 in complex with a binding protein has been solved [2].

Contents

Biological Role

The U4 snRNA has been shown to exist in a number of different formats including: bound to proteins as a small nuclear Ribo-Nuclear Protein snRNP[2], involved with the U6 snRNA in the di-snRNP[3], as well as involved with both the U6 snRNA and the U5 snRNA in the tri-snRNP.[4][5] The different formats have been proposed to coincide with different temporal events in the activity of the penta-snRNP[6], or as intermediates in the step-wise model of spliceosome assembly and activity.[7]

The U4 snRNA (and its likely analog snR14 in Yeast[8]) has been shown not to participate directly in the specific catalytic activities of the splicing reaction[9], and is proposed instead to act as a regulator of the U6 snRNA. The U4 snRNA inhibits spliceosome activity during assembly by complementary base pairing between the U6 snRNA in two highly conserved stem regions.[10] It is suggested that this base-pairing interaction prevents the U6 snRNA from assembling with the U2 snRNA into the conformation required for catalytic activity.[11] If the U4 snRNA is degraded and thereby removed from the spliceosome, splicing is effectively halted.[12] The U4 and U6 snRNAs are demonstratively required for splicing in vitro.[13]

Structure

Figure 1. Naked U4 putative secondary structure.
Figure 2. Putative U4/U6 base pairing secondary structure.

The U4 snRNA secondary structure is suggested to alter depending on its interaction with the U6 snRNA.[14] Several experiments involving X-ray crystallography[15][16], NMR[17], and chemical modification RNA structure probing[18] indicate that U4 snRNA secondary structure contains several conserved motifs[19], which serve structural as well as intermediary roles in establishing interactions with other splicing components. The putative U4/U6 snRNA base pairing secondary structure shown in Figure 2., is conserved across a diverse set of organisms suggesting the splicing machinery's ancient origins.[20] The naked U4 snRNA is currently under investigation[21] via chemical modification experiments, however it has been shown previously that a highly conserved Kinked-loop participates in specific protein interactions.[22][23]

Interactions

The U4 snRNA must be displaced from U6 snRNA in an ATP dependent process involving the protein Brr2 - before the spliceosome is made active.[24][25][26] A cycle has been proposed including both Brr2 as well as the protein prp24 which selectively re-anneals U4 to the U6 snRNA.[27][28][29][30] A ring of Sm proteins surround a conserved region of the U4 snRNA near the 3' end which are expected to promote favorable interactions between the different snRNPs as well as possibly protect the U4 snRNA from degredation by RNAse enzymes.[31][32] Over 100 proteins have been identified that participate in spliceosomal pathway, several proteins of varying size are also known to interact with the U4 snRNP.[33]

References

  1. ^ Vidovic I, Nottrott S, Hartmuth K, Lührmann R, Ficner R (2000). "Crystal structure of the spliceosomal 15.5kD protein bound to a U4 snRNA fragment.". Mol Cell 6 (6): 1331-42. PMID 11163207. 
  2. ^ Raghunathan, P.L., Guthrie, C. (1998) “RNA unwinding in U4/U6 snRNPs requires ATP hydrolysis and the DEIH-box splicing factor Brr2.”. Current Biology. Vol. 8:847-855.
  3. ^ Bringmann, B.N., Rinke, J., Reuter, R., Theissen, H., Luhrmann, R. (1984) “Evidence for the existence of snRNAs U4 and U6 in a single ribonucleoprotein complex and for their association by intermolecular base pairing.”. The EMBO Journal. Vol. 3:1357-1363.
  4. ^ Black, D.L., Pinto, A.L. (1989) “U5 small nuclear ribonucleoprotein: RNA structure analysis and ATP-dependent interaction with U4/U6.”. Mol. Cell. Biol. Vol. 9:3350.
  5. ^ Stevens, S., Barta, I., Ge, H., Moore, R., Young, M., Lee, T., Abelson, J. (2001) "Biochemical and genetic analyses of the U5, U6, and U4/U6•U5 small nuclear ribonucleoproteins from Saccharomyces cerevisiae.". RNA. Vol. 7:1543–1553.
  6. ^ Stevens, S., Ryan, D., Ge, H., Moore, R., Young, M., Lee, T., Abelson, J. (2002) “Composition and Functional Characterization of the Yeast Spliceosomal Penta-snRNP.”. Molecular Cell. Vol. 9:1;31-44.
  7. ^ Cheng, S., Abelson, J. (1987) “Spliceosome assembly in yeast.”. Genes and Development. Vol. 1:1014-1027.
  8. ^ Siliciano, P.G., Brow, D.A., Roiha, H., Guthrie, C. (1987) “An essential snRNA from S. cerevisiae has properties predicted for U4, including interaction with a U6-like snRNA.”. Cell. Vol. 14:50(4):585-592.
  9. ^ Yean, S.L., Lin, R.J. (1991) “U4 small nuclear RNA dissociates from a yeast splicesome and does not participate in the subsequent splicing reaction.”. Mol. Cell. Biol. Vol. 11:5571.
  10. ^ Guthrie, C., Patterson, B. (1998) “Spliceosomal snRNAs.”. Annu. Rev. Genet. Vol. 22:387.
  11. ^ Madhani, H.D., Guthrie, C. (1992) “A novel base-pairing interaction between U2 and U6 snRNAs suggests a mechanism for the catalytic activation of the spliceosome.”. Cell. Vol. 20:479.
  12. ^ Berget, S.M., Robberson, B.L. (1986) ”U1, U2, and U4/U6 small nuclear ribonucleoproteins are required for in vitro splicing but not polyadenylation.”. Cell. Vol. 46:692-696.
  13. ^ Black, D. L., Steitz, J.A. (1986) “Pre-mRNA splicing in vitro requires intact U4/U6 small nuclear ribonucleoprotein.”. Cell. Vol. 46:697-704.
  14. ^ Cheng, S., Abelson, J. (1987) “Spliceosome assembly in yeast.”. Genes and Development. Vol. 1:1014-1027.
  15. ^ Vidovic, I., Nottrott, S., Hartmuth, K., Lührmann, R., Ficner, R. (2000) “Crystal structure of the spliceosomal 15.5K protein bound to a U4 snRNA fragment.”. Mol. Cell. Vol. 6:1331–1342.
  16. ^ Kambach C., Walke,S. and Nagai,K. (1999) “Structure and assembly of the spliceosomal small ribonucleoprotein particles.”. Curr. Opin. Struct. Biol. Vol. 9:222–230.
  17. ^ Comolli, L.R., Ulyanov, N.B., Soto, A.M., Marky, L.A., James, T.L., Gmeiner, W.H. (2002) “NMR structure of the 2' stem-loop from human U4 snRNA.”. Nucleic Acids Res. Vol. 30:20;4371–4379.
  18. ^ Mougin, A., Gottschalk, A., Fabrizio, P., Lührmann, R., Branlant, C. (2002) “Direct probing of RNA structure and RNA-protein interactions in purified HeLa cell's and yeast spliceosomal U4/U6.U5 tri-snRNP particles.”. J Mol Biol. Vol. 12:317(5):631-49.
  19. ^ Li, L., Otake, L.R., Xu, Y.X., Michaeli, S. (2000) “The trans-Spliceosomal U4 RNA from the Monogenetic Trypanosomatid Leptomonas collosoma - CLONING AND IDENTIFICATION OF A TRANSCRIBED tRNA-LIKE ELEMENT THAT CONTROLS ITS EXPRESSION.”. J Biol Chem. Vol. 275:4;2259-2264.
  20. ^ Izquierdo, J.M., Valcárcel, J. (2006) "A simple principle to explain the evolution of pre-mRNA splicing.". Genes and Development. Vol. 23:150-151.
  21. ^ Unpublished Experimental Investigation
  22. ^ Boon, K.L., Norman, C., Grainger, R.J., Newman, A.J., Beggs, J.D. (2006) "Prp8p dissection reveals domain structure and protein interaction sites.". RNA. Vol. 12;198-205.
  23. ^ Vidovic, I., Nottrott, S., Hartmuth, K., Luhrmann, R., Ficner, R. (2000) "Crystal structure of the spliceosomal 15.5kD protein bound to a U4 snRNA fragment.". Mol Cell. Vol. 6:1331–1342.
  24. ^ Yean, S.L., Lin, R.J. (1991) “U4 small nuclear RNA dissociates from a yeast splicesome and does not participate in the subsequent splicing reaction.”. Mol. Cell. Biol. Vol. 11:5571.
  25. ^ Blencowe, B.J., Sproat, B.S., Ryder, U., Barabino, S., Lamond, A.I. (1989) “Anti-sense probing of the human U4/U6 snRNP with biotinylated 2'-OMe RNA oligonucleotides.”. Cell. Vol. 59:531.
  26. ^ Raghunathan, P.L., Guthrie, C.R. (1998) “Spliceosomal recycling factor that reanneals U4 and U6 small nuclear ribonucleoprotein particles.”. Science. Vol. 279: 857–860.
  27. ^ Fortner, D., Troy, G., Brow, D. (1994) "A stem loop in U6 RNA defines a conformational switch required for pre-mRNA splicing.". Genes & Development. Vol. 8: 221–233.
  28. ^ Jandrositz, A., Guthrie, C. (1995) "Evidence for a Prp24 binding site in U6 snRNA and in a putative intermediate in the annealing of U6 and U4 snRNAs.". The EMBO Journal. Vol. 14: 820–832.
  29. ^ Ghetti, A., Company, M., Abelson, J. (1995) "Specificity of Prp24 to RNA: A role for Prp24 in the dynamic interaction of U4 and U6 snRNAs.". RNA. Vol. 1:132–145.
  30. ^ Raghunathan, P.L., Guthrie, C.R. (1998) “Spliceosomal recycling factor that reanneals U4 and U6 small nuclear ribonucleoprotein particles.”. Science. Vol. 279: 857–860.
  31. ^ Urlaub, H., Raker, V.A., Kostka, S., Lührmann, R. (2001) “Sm protein−Sm site RNA interactions within the inner ring of the spliceosomal snRNP core structure.”. The EMBO Journal. Vol. 20:187–196.
  32. ^ Stark, H., Dube, P., Lührmann, R. Kastner, B. (2000) “The 3-D arrangement of RNA and proteins in the spliceosomal U1 snRNP.”. Nature. Vol. 409:539-542.
  33. ^ Nottrott, S., Urlaub, H., Lührmann, R. (2002) “Hierarchical, clustered protein interactions with U4/U6 snRNA: a biochemical role for U4/U6.”. Proteins. The EMBO Journal. Vol. 21:20;5527-5528.

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