Author:
Schneider Marc,Hsiao He-Hsuan,Will Cindy L,Giet Régis,Urlaub Henning,Lührmann Reinhard
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology
Reference49 articles.
1. Will, C.L. & Lührmann, R. Spliceosome structure and function. in The RNA World 3rd edn (eds. Gesteland, R.F., Cech, T.R. & Atkins, J.F.) 369–400 (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 2006).
2. Makarova, O.V., Makarov, E.M., Liu, S., Vornlocher, H.P. & Lührmann, R. Protein 61K, encoded by a gene (PRPF31) linked to autosomal dominant retinitis pigmentosa, is required for U4/U6*U5 tri-snRNP formation and pre-mRNA splicing. EMBO J. 21, 1148–1157 (2002).
3. Schaffert, N., Hossbach, M., Heintzmann, R., Achsel, T. & Lührmann, R. RNAi knockdown of hPRP31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies. EMBO J. 23, 3000–3009 (2004).
4. Vithana, E.N. et al. A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11). Mol. Cell 8, 375–381 (2001).
5. Mathew, R. et al. Phosphorylation of human PRP28 by SRPK2 is required for integration of the U4/U6–U5 tri-snRNP into the spliceosome. Nat. Struct. Mol. Biol. 15, 435–443 (2008).
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