Moore, M.J. & Proudfoot, N.J. Pre-mRNA processing alcove aback to archetype and advanced to translation. Corpuscle 136, 688–700 (2009).
Le Hir, H., Izaurralde, E., Maquat, L.E. & Moore, M.J. The spliceosome deposits assorted proteins 20–24 nucleotides upstream of mRNA exon-exon junctions. EMBO J. 19, 6860–6869 (2000).
Tange, T.Ø., Nott, A. & Moore, M.J. The ever-increasing complexities of the exon alliance complex. Curr. Opin. Corpuscle Biol. 16, 279–284 (2004).
Le Hir, H. & Andersen, G.R. Structural insights into the exon alliance complex. Curr. Opin. Struct. Biol. 18, 112–119 (2008).
Andersen, C.B. et al. Anatomy of the exon alliance amount circuitous with a trapped DEAD-box ATPase apprenticed to RNA. Science 313, 1968–1972 (2006).
Ballut, L. et al. The exon alliance amount circuitous is bound assimilate RNA by inhibition of eIF4AIII ATPase activity. Nat. Struct. Mol. Biol. 12, 861–869 (2005).
Bono, F., Ebert, J., Lorentzen, E. & Conti, E. The clear anatomy of the exon alliance circuitous reveals how it maintains a abiding anchor on mRNA. Corpuscle 126, 713–725 (2006).
Nielsen, K.H. et al. Apparatus of ATP about-face inhibition in the EJC. RNA 15, 67–75 (2009).
Gehring, N.H., Lamprinaki, S., Hentze, M.W. & Kulozik, A.E. The bureaucracy of exon-junction circuitous accumulation by the spliceosome explains key appearance of beastly nonsense-mediated mRNA decay. PLoS Biol. 7, e1000120 (2009).
Merz, C., Urlaub, H., Will, C.L. & Luhrmann, R. Protein agreement of beastly mRNPs spliced in vitro and cogwheel requirements for mRNP protein recruitment. RNA 13, 116–128 (2007).
Reichert, V.L., Le Hir, H., Jurica, M.S. & Moore, M.J. 5′ exon interactions aural the beastly spliceosome authorize a framework for exon alliance circuitous anatomy and assembly. Genes Dev. 16, 2778–2791 (2002).
Zhang, Z. & Krainer, A.R. Splicing remodels agent ribonucleoprotein architectonics via eIF4A3-dependent and -independent application of exon alliance circuitous components. Proc. Natl. Acad. Sci. USA 104, 11574–11579 (2007).
Barbosa, I. et al. Beastly CWC22 escorts the helicase eIF4AIII to spliceosomes and promotes exon alliance circuitous assembly. Nat. Struct. Mol. Biol. 19, 983–990 (2012).
Gehring, N.H., Lamprinaki, S., Kulozik, A.E. & Hentze, M.W. Disassembly of exon alliance complexes by PYM. Corpuscle 137, 536–548 (2009).
Hwang, J. & Maquat, L.E. Nonsense-mediated mRNA adulteration (NMD) in beastly embryogenesis: to die or not to die, that is the question. Curr. Opin. Genet. Dev. 21, 422–430 (2011).
Rebbapragada, I. & Lykke-Andersen, J. Execution of nonsense-mediated mRNA decay: what defines a substrate? Curr. Opin. Corpuscle Biol. 21, 394–402 (2009).
Isken, O. & Maquat, L.E. The assorted lives of NMD factors: acclimation roles in gene and genome regulation. Nat. Rev. Genet. 9, 699–712 (2008).
Saulière, J. et al. The exon alliance circuitous differentially marks spliced junctions. Nat. Struct. Mol. Biol. 17, 1269–1271 (2010).
Ashton-Beaucage, D. et al. The exon alliance circuitous controls the splicing of MAPK and added continued intron-containing transcripts in Drosophila. Corpuscle 143, 251–262 (2010).
Michelle, L. et al. Proteins associated with the exon alliance circuitous additionally ascendancy the another splicing of apoptotic regulators. Mol. Cell. Biol. 32, 954–967 (2012).
Roignant, J.Y. & Treisman, J.E. Exon alliance circuitous subunits are appropriate to braid Drosophila MAP kinase, a ample heterochromatic gene. Corpuscle 143, 238–250 (2010).
Hachet, O. & Ephrussi, A. Splicing of oskar RNA in the basis is accompanying to its cytoplasmic localization. Nature 428, 959–963 (2004).
Haremaki, T., Sridharan, J., Dvora, S. & Weinstein, D.C. Adjustment of bearcat embryogenesis by the exon alliance circuitous amount basic Eif4a3. Dev. Dyn. 239, 1977–1987 (2010).
Silver, D.L. et al. The exon alliance circuitous basic Magoh controls academician admeasurement by acclimation neural axis corpuscle division. Nat. Neurosci. 13, 551–558 (2010).
Albers, C.A. et al. Compound bequest of a low-frequency authoritative SNP and a attenuate absent alteration in exon-junction circuitous subunit RBM8A causes TAR syndrome. Nat. Genet. 44, 435–439 (2012).
Darnell, R.B. HITS-CLIP: across-the-board angle of protein-RNA adjustment in active cells. Wiley Interdiscip Rev. RNA 1, 266–286 (2010).
Ule, J., Jensen, K., Mele, A. & Darnell, R.B. CLIP: a adjustment for anecdotic protein-RNA alternation sites in active cells. Methods 37, 376–386 (2005).
Ule, J. et al. CLIP identifies Nova-regulated RNA networks in the brain. Science 302, 1212–1215 (2003).
Kent, W.J. BLAT—the BLAST-like alignment tool. Genome Res. 12, 656–664 (2002).
Zhang, C. & Darnell, R.B. Mapping in vivo protein-RNA interactions at single-nucleotide resolution from HITS-CLIP data. Nat. Biotechnol. 29, 607–614 (2011).
Fejes, A.P. et al. FindPeaks 3.1: a apparatus for anecdotic areas of accessory from massively alongside short-read sequencing technology. Bioinformatics 24, 1729–1730 (2008).
Patel, A.A. & Steitz, J.A. Splicing double: insights from the additional spliceosome. Nat. Rev. Mol. Corpuscle Biol. 4, 960–970 (2003).
Hirose, T., Shu, M.D. & Steitz, J.A. Splicing of U12-type introns deposits an exon alliance circuitous competent to abet nonsense-mediated mRNA decay. Proc. Natl. Acad. Sci. USA 101, 17976–17981 (2004).
Dostie, J. & Dreyfuss, G. Adaptation is appropriate to abolish Y14 from mRNAs in the cytoplasm. Curr. Biol. 12, 1060–1067 (2002).
Lejeune, F., Ishigaki, Y., Li, X. & Maquat, L.E. The exon alliance circuitous is detected on CBP80-bound but not eIF4E-bound mRNA in beastly cells: dynamics of mRNP remodeling. EMBO J. 21, 3536–3545 (2002).
Dennis, G. Jr. et al. DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biol. 4, 3 (2003).
Huang, W., Sherman, B.T. & Lempicki, R.A. Systematic and commutual assay of ample gene lists application DAVID bioinformatics resources. Nat. Protoc. 4, 44–57 (2009).
Sanford, J.R. et al. Splicing agency SFRS1 recognizes a functionally assorted mural of RNA transcripts. Genome Res. 19, 381–394 (2009).
Bailey, T.L., Boden, M., Whitington, T. & Machanick, P. The amount of position-specific priors in burden analysis application MEME. BMC Bioinformatics 11, 179 (2010).
Long, J.C. & Caceres, J.F. The SR protein ancestors of splicing factors: adept regulators of gene expression. Biochem. J. 417, 15–27 (2009).
Markham, N.R. & Zuker, M. DINAMelt web server for nucleic acerbic melting prediction. Nucleic Acids Res. 33, W577–W581 (2005).
Markham, N.R. & Zuker, M. UNAFold: software for nucleic acerbic folding and hybridization. Methods Mol. Biol. 453, 3–31 (2008).
Mishler, D.M., Christ, A.B. & Steitz, J.A. Flexibility in the armpit of exon alliance circuitous degradation appear by anatomic accumulation and RNA accessory anatomy alterations in the splicing substrate. RNA 14, 2657–2670 (2008).
Budiman, M.E. et al. Eukaryotic admission agency 4a3 is a selenium-regulated RNA-binding protein that selectively inhibits selenocysteine incorporation. Mol. Corpuscle 35, 479–489 (2009).
Le Hir, H. & Seraphin, B. EJCs at the affection of translational control. Corpuscle 133, 213–216 (2008).
Nagy, E. & Maquat, L.E. A aphorism for termination-codon position aural intron-containing genes: back nonsense affects RNA abundance. Trends Biochem. Sci. 23, 198–199 (1998).
Bühler, M., Paillusson, A. & Muhlemann, O. Efficient downregulation of immunoglobulin mu mRNA with abortive translation-termination codons requires the 5′-half of the VDJ exon. Nucleic Acids Res. 32, 3304–3315 (2004).
Carter, M.S., Li, S. & Wilkinson, M.F. A splicing-dependent authoritative apparatus that detects adaptation signals. EMBO J. 15, 5965–5975 (1996).
Holbrook, J.A., Neu-Yilik, G., Hentze, M.W. & Kulozik, A.E. Nonsense-mediated adulteration approaches the clinic. Nat. Genet. 36, 801–808 (2004).
Viegas, M.H., Gehring, N.H., Breit, S., Hentze, M.W. & Kulozik, A.E. The affluence of RNPS1, a protein basic of the exon alliance complex, can actuate the airheadedness in ability of the nonsense advised adulteration pathway. Nucleic Acids Res. 35, 4542–4551 (2007).
Zetoune, A.B. et al. Comparison of nonsense-mediated mRNA adulteration ability in assorted murine tissues. BMC Genet. 9, 83 (2008).
Zhang, Z. & Krainer, A.R. Involvement of SR proteins in mRNA surveillance. Mol. Corpuscle 16, 597–607 (2004).
Daguenet, E. et al. Perispeckles are above accumulation sites for the exon alliance amount complex. Mol. Biol. Corpuscle 23, 1765–1782 (2012).
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