| 1 | PRPF8, SLU7
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| Dynamic protein-RNA interactions in mediating splicing catalysis.
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| Chung CS, Tseng CK, Lai YH, Wang HF, Newman AJ, Cheng SC.
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| Nucleic Acids Res 47(2):899-910. doi: 10.1093/nar/gky1089.
2019
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| 2 | PRPF8, SNRNP200
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| Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.
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| Escher P, Passarin O, Munier FL, Tran VH, Vaclavik V.
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| Ophthalmic Genet 39(1):80-86. doi: 10.1080/13816810.2017.1393825. Epub 2017 Oct 31.
2018
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| 3 | GRIA1, PRPF8
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| When pitch adds to volume: coregulation of transcript diversity predicts gene function
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| Cáceres A, González JR.
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| BMC Genomics. Dec 13;19(1):926. doi: 10.1186/s12864-018-5263-z. 2018
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| 4 | EFTUD2, PRPF8, SNRNP200
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| Assembly of the U5 snRNP component PRPF8 is controlled by the HSP90/R2TP chaperones.
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| Malinová A, Cvačková Z, Matějů D, Hořejší Z, Abéza C, Vandermoere F, Bertrand E, Staněk D, Verheggen C.
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| J Cell Biol 216(6):1579-1596. doi: 10.1083/jcb.201701165. Epub 2017 May 17.
2017
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| 5 | PRPF18, PRPF8, SLU7
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| Structure of a spliceosome remodelled for exon ligation.
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| Fica SM, Oubridge C, Galej WP, Wilkinson ME, Bai XC, Newman AJ, Nagai K.
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| Nature 542(7641):377-380. doi: 10.1038/nature21078. Epub 2017 Jan 11.
2017
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| 6 | CWC22, PRPF8, RBM22, SLU7
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| An Atomic Structure of the Human Spliceosome.
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| Zhang X, Yan C, Hang J, Finci LI, Lei J, Shi Y.
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| Cell 169(5):918-929.e14. doi: 10.1016/j.cell.2017.04.033. Epub 2017 May 11. 2017
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| 7 | PRPF3, PRPF31, PRPF8, RP11, RP13, RP18
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| Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epithelium.
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| Farkas MH, Lew DS, Sousa ME, Bujakowska K, Chatagnon J, Bhattacharya SS, Pierce EA, Nandrot EF.
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| Am J Pathol 184(10):2641-52. doi: 10.1016/j.ajpath.2014.06.026.
2014
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| 8 | PRPF8, SNW1
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| SNW1 enables sister chromatid cohesion by mediating the splicing of sororin and APC2 pre-mRNAs.
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| van der Lelij P, Stocsits RR, Ladurner R, Petzold G, Kreidl E, Koch B, Schmitz J, Neumann B, Ellenberg J, Peters JM.
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| EMBO J 33(22):2643-58. doi: 10.15252/embj.201488202. Epub 2014 Sep 25.
2014
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| 9 | PRPF8, SNRNP200
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| Inhibition of RNA helicase Brr2 by the C-terminal tail of the spliceosomal protein Prp8.
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| Mozaffari-Jovin S, Wandersleben T, Santos KF, Will CL, Lührmann R, Wahl MC.
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| Science 341(6141):80-4. doi: 10.1126/science.1237515. Epub 2013 May 23.
2013
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| 10 | DHX16, DHX38, GPKOW, PRPF8, PRPF8, SLU7
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| Dynamic protein-protein interaction wiring of the human spliceosome.
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| Hegele A, Kamburov A, Grossmann A, Sourlis C, Wowro S, Weimann M, Will CL, Pena V, Lührmann R, Stelzl U.
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| Mol Cell 45(4):567-80. doi: 10.1016/j.molcel.2011.12.034.
2012
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| 11 | PRPF3, PRPF31, PRPF8, RP11, RP13, RP18
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| PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa.
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| Tanackovic G, Ransijn A, Thibault P, Abou Elela S, Klinck R, Berson EL, Chabot B, Rivolta C.
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| Hum Mol Genet 20(11):2116-30. Epub 2011 Mar 5.
2011
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| 12 | PRPF3, PRPF31, PRPF8
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| Temporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RP.
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| Cao H, Wu J, Lam S, Duan R, Newnham C, Molday RS, Graziotto JJ, Pierce EA, Hu J.
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| PLoS One 6(1):e15860.
2011
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| 13 | PRPF8, RP13
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| Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes.
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| Towns KV, Kipioti A, Long V, McKibbin M, Maubaret C, Vaclavik V, Ehsani P, Springell K, Kamal M, Ramesar RS, Mackey DA, Moore AT, Mukhopadhyay R, Webster AR, Black GC, O'Sullivan J, Bhattacharya SS, Pierce EA, Beggs JD, Inglehearn CF.
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| Hum Mutat 31(5):E1361-76.
2010
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| 14 | RP9, RP11, RP13, RP18, PRPF3, PRPF8, PRPF31
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| Transcriptional expression of cis-acting and trans-acting splicing mutations cause autosomal dominant retinitis pigmentosa.
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| Gamundi MJ, Hernan I, Muntanyola M, Maseras M, L—pez-Romero P, Alvarez R, Dopazo A, Borrego S, Carballo M.
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| Hum Mutat 29(6):869-78. 2008
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| 15 | PRPF8
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| Structural elucidation of a PRP8 core domain from the heart of the spliceosome.
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| Ritchie DB, Schellenberg MJ, Gesner EM, Raithatha SA, Stuart DT, Macmillan AM.
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| Nat Struct Mol Biol 15(11):1199-205. Epub 2008 Oct 2.
2008
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| 16 | PRPF8
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| Structure and function of an RNase H domain at the heart of the spliceosome.
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| Pena V, Rozov A, Fabrizio P, Lührmann R, Wahl MC.
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| EMBO J 27(21):2929-40. Epub 2008 Oct 9.
2008
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| 17 | PRPF8
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| Structure of a multipartite protein-protein interaction domain in splicing factor prp8 and its link to retinitis pigmentosa.
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| Pena V, Liu S, Bujnicki JM, Luhrmann R, Wahl MC.
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| Mol Cell 25(4):615-24. 2007
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| 18 | PRPF8, RP13
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| prp8 mutations that cause human retinitis pigmentosa lead to a U5 snRNP maturation defect in yeast.
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| Boon KL, Grainger RJ, Ehsani P, Barrass JD, Auchynnikava T, Inglehearn CF, Beggs JD.
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| Nat Struct Mol Biol 14(11):1077-1083. Epub 2007 Oct 14. 2007
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| 19 | PRPF8
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| Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.
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| Testa F, Ziviello C, Rinaldi M, Rossi S, Di Iorio V, Interlandi E, Ciccodicola A, Banfi S, Simonelli F.
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| Eur J Ophthalmol 16(5):779-81. 2006
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| 20 | PRPF8
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| ARP2 a novel protein involved in apoptosis of LNCaP cells shares a high degree homology with splicing factor Prp8.
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| Tapia-Vieyra JV, Arellano RO, Mas-Oliva J.
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| Mol Cell Biochem 269(1-2):189-201. 2005
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| 21 | PRPF3,PRPF31,PRPF8
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| Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.
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| Martinez-Gimeno M, Gamundi MJ, Hernan I, Maseras M, Milla E, Ayuso C, Garcia-Sandoval B, Beneyto M, Vilela C, Baiget M, Antinolo G, Carballo M.
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| Invest Ophthalmol Vis Sci 44(5):2171-7. 2003
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| 22 | PRPF8, RP13
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| Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13).
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| van Lith-Verhoeven JJ, van der Velde-Visser SD, Sohocki MM, Deutman AF, Brink HM, Cremers FP, Hoyng CB.
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| Ophthalmic Genet 23(1):1-12. 2002
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| 23 | PRPF8
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| Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).
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| McKie AB, McHale JC, Keen TJ, Tarttelin EE, Goliath R, van Lith-Verhoeven JJ, Greenberg J, Ramesar RS, Hoyng CB, Cremers FP, Mackey DA, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF.
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| Hum Mol Genet 10(15):1555-62. 2001
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| 24 | PRPF3,PRPF8,PRPF31
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| Mapping of the human HPRP3 and HPRP4 genes encoding U4/U6-associated splicing factors to chromosomes 1q21.1 and 9q31-q33.
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| Heng HH, Wang A, Hu J.
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| Genomics 48(2):273-5. No abstract available. 1998
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| 25 | PRPF8, SNRNP40
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| The human U5-220kD protein (hPrp8) forms a stable RNA-free complex with several U5-specific proteins, including an RNA unwindase, a homologue of ribosomal elongation factor EF-2, and a novel WD-40 protein.
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| Achsel T, Ahrens K, Brahms H, Teigelkamp S, Luhrmann R.
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| Mol Cell Biol 18(11):6756-66. 1998
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| 26 | PRPF3,PRPF8,PRPF31
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| Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome.
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| Wang A, Forman-Kay J, Luo Y, Luo M, Chow YH, Plumb J, Friesen JD, Tsui LC, Heng HH, Woolford JL Jr, Hu J.
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| Hum Mol Genet 6(12):2117-26. 1997
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