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Spliceosome Structure and Function
Open accessAbstract
Pre-mRNA splicing is catalyzed by the spliceosome, a multimegadalton ribonucleoprotein (RNP) complex comprised of five snRNPs and numerous proteins. Intricate RNA-RNA and RNP networks, which serve to align the reactive groups of the pre-mRNA for catalysis, are formed and repeatedly rearranged during spliceosome assembly and catalysis. Both the conformation and composition of the spliceosome are highly dynamic, affording the splicing machinery its accuracy and flexibility, and these remarkable dynamics are largely conserved between yeast and metazoans. Because of its dynamic and complex nature, obtaining structural information about the spliceosome represents a major challenge. Electron microscopy has revealed the general morphology of several spliceosomal complexes and their snRNP subunits, and also the spatial arrangement of some of their components. X-ray and NMR studies have provided high resolution structure information about spliceosomal proteins alone or complexed with one or more binding partners. The extensive interplay of RNA and proteins in aligning the pre-mRNA's reactive groups, and the presence of both RNA and protein at the core of the splicing machinery, suggest that the spliceosome is an RNP enzyme. However, elucidation of the precise nature of the spliceosome's active site, awaits the generation of a high-resolution structure of its RNP core.
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“Alternative splicing patterns (BOX 1) are regulated by specialized pre-mRNA binding proteins that alter spliceosome assembly at specific splice sites5–8”
From The neurogenetics of alternative splicing (2016) · cites this paper as [5]
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Lysine acetylation targets protein complexes and co-regulates major cellular functions
Choudhary, C., Kumar, C., Gnad, F., Nielsen, M. L., Rehman, M., Walther, T. C., Olsen, J. V., & Mann, M. (2009) · Science · doi:10.1126/science.1175371 · Cited by 4,040
Mechanisms of Alternative Pre-Messenger RNA Splicing
Black, D. L. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161720 · Cited by 2,704
The Spliceosome: Design Principles of a Dynamic RNP Machine
Wahl, M. C., Will, C. L., & Lührmann, R. (2009) · Cell · doi:10.1016/j.cell.2009.02.009 · Cited by 2,665
Self-citationExpansion of the eukaryotic proteome by alternative splicing
Nilsen, T. W., & Graveley, B. R. (2010) · Nature · doi:10.1038/nature08909 · Cited by 2,254
Understanding alternative splicing: towards a cellular code
Matlin, A. J., Clark, F., & Smith, C. W. J. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1645 · Cited by 1,299
Mechanisms of alternative splicing regulation: insights from molecular and genomics approaches
Chen, M., & Manley, J. L. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2777 · Cited by 1,284
An extensive network of coupling among gene expression machines
Maniatis, T., & Reed, R. (2002) · Nature · doi:10.1038/416499a · Cited by 1,148
Mechanical Devices of the Spliceosome: Motors, Clocks, Springs, and Things
Staley, J. P., & Guthrie, C. (1998) · Cell · doi:10.1016/s0092-8674(00)80925-3 · Cited by 1,133
Splicing regulation: From a parts list of regulatory elements to an integrated splicing code
Wang, Z., & Burge, C. B. (2008) · RNA · doi:10.1261/rna.876308 · Cited by 1,127
Exon Recognition in Vertebrate Splicing
Berget, S. M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.6.2411 · Cited by 1,090
Research works printed but not linked: 1
- Stark H, Lührmann R 2006. Electron cryomicroscopy of spliceosomal components. Ann Rev Biophy Biomol Struct 35: 435–457 [DOI] [PubMed] [Google Scholar]
Cited by
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Items 601–700 of 1,001
An overview of transcription in dinoflagellates
Zaheri, B., & Morse, D. (2022) · Gene · doi:10.1016/j.gene.2022.146505 · Cited by 23
Park, B., Tachi-Duprat, M., Ihewulezi, C., Devotta, A., & Saint‐Jeannet, J. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10030029 · Cited by 23
Zheng, J., Wu, S., Tang, M., Xi, S., Wang, Y., Ren, J., Luo, H., Hu, P., Sun, L.-Z., Du, Y., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06210-3 · Cited by 24
Vitamin D and alternative splicing of RNA
Zhou, R., Chun, R. F., Lisse, T. S., Garcia, A. J., Xu, J., Adams, J. S., & Hewison, M. (2014) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2014.09.025 · Cited by 23
Hodson, M. J., Hudson, A. J., Cherny, D., & Eperon, I. C. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks322 · Cited by 23
The role of mRNA splicing in prostate cancer
Lapuk, A. V., Volik, S. V., Wang, Y. Z., & Collins, C. (2014) · Asian Journal of Andrology · doi:10.4103/1008-682x.127825 · Cited by 25
Kanno, T., Lin, W., Fu, J. L., Matzke, A. J. M., & Matzke, M. A. (2017) · RNA · doi:10.1261/rna.060517.116 · Cited by 23
Identification of a noncanonical RNA binding domain in the U2 snRNP protein SF3A1
Martelly, W., Fellows, B., Senior, K., Marlowe, T. A., & Sharma, S. (2019) · RNA · doi:10.1261/rna.072256.119 · Cited by 24
Hudson, A. J., Moore, A. N., Elniski, D., Joseph, J., Yee, J., & Russell, A. G. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks887 · Cited by 24
Role of PRMT1 and PRMT5 in Breast Cancer
Martinez, S., Sentis, S., Poulard, C., Trédan, O., & Romancer, M. L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168854 · Cited by 25
Liu, J., Ma, T., Gao, M., Liu, Y., Liu, J., Wang, S., Xie, Y., Wen, Q., Wang, L., Cheng, J., et al. (2020) · Frontiers in Public Health · doi:10.3389/fpubh.2020.584964 · Cited by 22
Weng, X., Zhou, X., Xie, S., Gu, J., & Wang, Z. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2021.01.016 · Cited by 24
Therapeutic Targeting of Alternative RNA Splicing in Gastrointestinal Malignancies and Other Cancers
Şahin, İ., George, A., & Seyhan, A. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111790 · Cited by 22
Wang, H., Xu, F., Lu, L., Yang, F., Huang, X., Lv, L., Hu, H., & Jiang, Y. (2021) · Journal of Cancer · doi:10.7150/jca.65225 · Cited by 23
Arthur, G. K., & Cruse, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020788 · Cited by 24
RBM22, a Key Player of Pre-mRNA Splicing and Gene Expression Regulation, Is Altered in Cancer
Soubise, B., Jiang, Y., Douet‐Guilbert, N., & Troadec, M. (2022) · Cancers · doi:10.3390/cancers14030643 · Cited by 23
Oladokun, S., Clark, K. F., & Adewole, D. I. (2022) · Microorganisms · doi:10.3390/microorganisms10050861 · Cited by 22
Zhang, X., Zhang, X., Yuan, J., & Li, F. (2023) · Genes · doi:10.3390/genes14071473 · Cited by 22
Baumgartner, M., Lemoine, C., Seesi, S. A., Karunakaran, D. K. P., Sturrock, N., Banday, A. R., Kilcollins, A. M., Măndoiu, I., & Kanadia, R. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22257 · Cited by 24
Spliceozymes: Ribozymes that Remove Introns from Pre-mRNAs in Trans
Amini, Z. N., Olson, K. E., & Müller, U. F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101932 · Cited by 22
Succession of splicing regulatory elements determines cryptic 5′ss functionality
Brillen, A.-L., Schöneweis, K., Walotka, L., Hartmann, L., Müller, L., Ptok, J., Kaisers, W., Poschmann, G., Stühler, K., Buratti, E., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1317 · Cited by 22
Lee, S., & Stevens, S. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605113113 · Cited by 22
Xie, S., Yang, X., Wang, D., Zhu, F., Yang, N., Hou, Z., & Ning, Z. (2018) · PLoS ONE · doi:10.1371/journal.pone.0191096 · Cited by 22
Ghosh, A. K., Reddy, G. C., Kovela, S., Relitti, N., Urabe, V. K., Prichard, B. E., & Jurica, M. S. (2018) · Organic Letters · doi:10.1021/acs.orglett.8b03228 · Cited by 22
Human RNF113A participates of pre‐mRNA splicing in vitro
Silva, G. K., Jurica, M. S., da Cunha, J. P. C., Oliveira, C. C., & Coltri, P. P. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28163 · Cited by 22
Small non-coding RNA within the endogenous spliceosome and alternative splicing regulation
Sperling, R. (2019) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2019.07.007 · Cited by 22
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Ghaemi, Z., Peterson, J. R., Gruebele, M., & Luthey-Schulten, Z. A. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007717 · Cited by 24
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Hajieghrari, B., & Farrokhi, N. (2020) · Plant Molecular Biology Reporter · doi:10.1007/s11105-020-01228-9 · Cited by 22
Wood, K., Rowlands, C. F., Thomas, H. B., Woods Jon, S., O’Flaherty, J., Douzgou, S., Kimber, S. J., Newman, W. G., & O’Keefe, R. T. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233582 · Cited by 22
Foessl, I., Bassett, J. H. D., Bjørnerem, Å., Busse, B., Calado, Â., Chavassieux, P., Christou, M., Douni, E. K., Fiedler, I. A. K., Fonseca, J. E., et al. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.720728 · Cited by 22
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Wang, L., Ruan, Y., Wu, X., & Zhou, X. (2022) · Journal of Immunology Research · doi:10.1155/2022/4163198 · Cited by 21
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Nguyễn, T. D., Carrascal, M., Vidal-Cortes, O., Gallardo, Ó., Casas, V., Gay, M., Phan, V. C., & Abián, J. (2015) · Journal of Proteomics · doi:10.1016/j.jprot.2015.10.029 · Cited by 21
Haraguchi, N., Shimada, M. K., Taniguchi, I., Ohno, M., & Mayeda, A. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.05.112 · Cited by 21
Brillen, A.-L., Walotka, L., Hillebrand, F., Müller, L., Widera, M., Theiss, S., & Schaal, H. (2017) · Journal of Virology · doi:10.1128/jvi.00389-17 · Cited by 22
Ghosh, A. K., Reddy, G. C., MacRae, A. J., & Jurica, M. S. (2017) · Organic Letters · doi:10.1021/acs.orglett.7b03456 · Cited by 21
Biamonti, G., Maita, L., & Montecucco, A. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00408 · Cited by 22
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Stanek, K. A., Patterson, J. A. K., Randolph, P. S., & Mura, C. (2017) · Acta Crystallographica Section D Structural Biology · doi:10.1107/s2059798317000031 · Cited by 20
Jackson, T. C., & Kochanek, P. M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00126 · Cited by 21
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Floro, J., Dai, A., Metzger, A., Mora-Martin, A., Ganem, N. J., Cifuentes, D., Wu, C.-S. P., Dalal, J. S., Lyons, S. M., Labadorf, A. T., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab647 · Cited by 18
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Wang, Z., Hong, Y., Yao, J., Huang, H., Qian, B., Liu, X., Chen, Y., Pang, J., Zhan, X., Zhu, J., et al. (2022) · Plant Cell & Environment · doi:10.1111/pce.14386 · Cited by 20
Mo, Z., Li, R., Cao, C., Li, Y., Zheng, S., Wu, R., Xue, J., Hu, J., Meng, H., Zhai, H., et al. (2023) · Environmental Toxicology · doi:10.1002/tox.23745 · Cited by 19
Wang, N., Hu, Y., & Wang, Z. (2023) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1815 · Cited by 26
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Tei, S., Ishii, H. T., Mitsuhashi, H., & Ishiura, S. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.04.035 · Cited by 20
Price, A., Görnemann, J., Guthrie, C., & Brow, D. A. (2013) · RNA · doi:10.1261/rna.041970.113 · Cited by 20
Jacobs, J., Marx, C., Kock, V., Reifschneider, O., Fränzel, B., Krisp, C., Wolters, D. A., & Kück, U. (2013) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m112.026583 · Cited by 20
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Larson, A., Fair, B. J., & Pleiss, J. A. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.027508 · Cited by 20
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Kanno, T., Lin, W., Chang, C., Matzke, M. A., & Matzke, A. J. M. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200022 · Cited by 19
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Bortoli, F. D., Neumann, A., Kotte, A., Timmermann, B., Schüler, T., Wahl, M. C., Loll, B., & Heyd, F. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz243 · Cited by 19
González‐López, Ó., Muñoz‐González, J. I., Órfão, A., Álvarez‐Twöse, I., & García‐Montero, A. C. (2022) · Cancers · doi:10.3390/cancers14102487 · Cited by 21
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Valdés, J., Nozaki, T., Sato, E., Chiba, Y., Nakada‐Tsukui, K., Villegas‐Sepúlveda, N., Winkler, R., Azuara-Liceaga, E. I., Mendoza-Figueroa, M. S., Watanabe, N., et al. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.07.027 · Cited by 19
Chiang, T.-W. W., & Cheng, S.-C. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00035-13 · Cited by 19
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Huang, S., Balgi, A. D., Pan, Y., Li, M., Zhang, X., Du, L., Zhou, M., Roberge, M., & Li, X. (2016) · Molecular Plant · doi:10.1016/j.molp.2016.10.006 · Cited by 18
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Norppa, A. J., Kauppala, T., Heikkinen, H. A., Verma, B., Iwaï, H., & Frilander, M. J. (2017) · RNA · doi:10.1261/rna.062844.117 · Cited by 19
Telekawa, C., Boisvert, F., & Bachand, F. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky915 · Cited by 18
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Tresini, M., Marteijn, J. A. F., & Vermeulen, W. (2016) · RNA Biology · doi:10.1080/15476286.2016.1142039 · Cited by 19
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Brant, A. C., Majerčiak, V., Moreira, M. Â. M., & Zheng, Z. (2019) · Virologica Sinica · doi:10.1007/s12250-019-00098-0 · Cited by 19
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Metadata
- Authors
- Will, C. L., & Luhrmann, R.
- Affiliations
- Max Planck Institute for Biophysical Chemistry (DE)
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2010-12-30
- Volume
- 3
- Issue
- 7
- Pages
- a003707-a003707
- ISSN
- 1943-0264 (ISSN-L)
- PMC
- PMC3119917
- OpenAlex
- W2148393113
- Cited by
- 1,829
- References
- 163
- Citations by year
- 2026: 89 · 2025: 130 · 2024: 141 · 2023: 135 · 2022: 127 · 2021: 170 · 2020: 142 · 2019: 141 · 2018: 122 · 2017: 111 · 2016: 123 · 2015: 100 · 2014: 91 · 2013: 77 · 2012: 63
- Type
- posted content
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Cold Spring Harbor Perspectives in Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- spliceosome, pre-mRNA splicing, small nuclear ribonucleoproteins, ribonucleoprotein complexes, spliceosome assembly, RNA-RNA interactions, spliceosome structure, active site, RNA-protein interactions
- MeSH terms
- Humans, Models, Genetic, Models, Molecular, Nucleic Acid Conformation, Protein Processing, Post-Translational, Ribonucleoproteins, RNA Precursors, RNA Splicing, Spliceosomes, Ribonucleoproteins, Small Nuclear, Protein Structure, Tertiary, Crystallography, X-Ray, Nuclear Magnetic Resonance, Biomolecular, Catalytic Domain
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