A Comprehensive Interaction Map of the Human Survival of Motor Neuron (SMN) Complex*
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Utz Fischer | Albert Sickmann | Ashwin Chari | A. Sickmann | U. Fischer | M. Grimmler | Simon Otter | Matthias Grimmler | Nils Neuenkirchen | A. Chari | Nils Neuenkirchen | Simon Otter
[1] R. Lührmann,et al. snRNP Sm proteins share two evolutionarily conserved sequence motifs which are involved in Sm protein‐protein interactions. , 1995, The EMBO journal.
[2] Utz Fischer,et al. Phosphorylation regulates the activity of the SMN complex during assembly of spliceosomal U snRNPs , 2005, EMBO reports.
[3] Lili Wan,et al. The Gemin5 protein of the SMN complex identifies snRNAs. , 2006, Molecular cell.
[4] Utz Fischer,et al. Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs , 2002, The EMBO journal.
[5] R. Lührmann,et al. The snRNP core assembly pathway: identification of stable core protein heteromeric complexes and an snRNP subcore particle in vitro. , 1996, The EMBO journal.
[6] G. Dreyfuss,et al. The Spinal Muscular Atrophy Disease Gene Product, SMN, and Its Associated Protein SIP1 Are in a Complex with Spliceosomal snRNP Proteins , 1997, Cell.
[7] J. Rappsilber,et al. Gemin8 Is a Novel Component of the Survival Motor Neuron Complex and Functions in Small Nuclear Ribonucleoprotein Assembly* , 2006, Journal of Biological Chemistry.
[8] A. Matera,et al. Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein. , 2001, Genes & development.
[9] G. Meister,et al. SMN-mediated assembly of RNPs: a complex story. , 2002, Trends in cell biology.
[10] U. Fischer,et al. Unrip, a factor implicated in cap-independent translation, associates with the cytosolic SMN complex and influences its intracellular localization. , 2005, Human molecular genetics.
[11] G. Meister,et al. Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins. , 2000, Human molecular genetics.
[12] Roger Brent,et al. C dil, a Human Gl and S Phase Protein Phosphatase That Associates with Cdk2 , 2003 .
[13] Livio Pellizzoni,et al. Identification and Characterization of Gemin7, a Novel Component of the Survival of Motor Neuron Complex* , 2002, The Journal of Biological Chemistry.
[14] B. Kastner,et al. Spliceosomal U snRNP Core Assembly: Sm Proteins Assemble onto an Sm Site RNA Nonanucleotide in a Specific and Thermodynamically Stable Manner , 1999, Molecular and Cellular Biology.
[15] Utz Fischer,et al. Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing. , 2003, Genes & development.
[16] A. Matera,et al. Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[17] G. Dreyfuss,et al. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[18] J. Yong,et al. Essential Role for the SMN Complex in the Specificity of snRNP Assembly , 2002, Science.
[19] A. Shevchenko,et al. Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems. , 1999, The Journal of cell biology.
[20] J. Weissenbach,et al. Identification and characterization of a spinal muscular atrophy-determining gene , 1995, Cell.
[21] K. Nagai,et al. Crystal Structures of Two Sm Protein Complexes and Their Implications for the Assembly of the Spliceosomal snRNPs , 1999, Cell.
[22] Usha Narayanan,et al. SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin beta. , 2002, Human molecular genetics.
[23] M. Brasch,et al. Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation? , 2000, Human molecular genetics.
[24] J. Rappsilber,et al. Unrip is a component of SMN complexes active in snRNP assembly , 2005, FEBS letters.
[25] H. Stark,et al. The Sm domain is an ancient RNA-binding motif with oligo(U) specificity , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[26] C. Lorson,et al. SMN oligomerization defect correlates with spinal muscular atrophy severity , 1998, Nature Genetics.
[27] Usha Narayanan,et al. Coupled in vitro import of U snRNPs and SMN, the spinal muscular atrophy protein. , 2004, Molecular cell.
[28] Arnold Munnich,et al. Correlation between severity and SMN protein level in spinal muscular atrophy , 1997, Nature Genetics.
[29] G. Meister,et al. A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs , 2001, Nature Cell Biology.
[30] B. Séraphin. Sm and Sm‐like proteins belong to a large family: identification of proteins of the U6 as well as the U1, U2, U4 and U5 snRNPs. , 1995, The EMBO journal.
[31] A. Shevchenko,et al. Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli. , 2000, The Journal of cell biology.
[32] G. Dreyfuss,et al. The SMN complex. , 2004, Experimental cell research.
[33] G. Dreyfuss,et al. Gemins modulate the expression and activity of the SMN complex. , 2005, Human molecular genetics.
[34] T. Richmond,et al. Baculovirus expression system for heterologous multiprotein complexes , 2004, Nature Biotechnology.