Macromolecular complexes: SMN - The master assembler

Current Biology

Volumn 11, Issue 21, 2001, Pages

  Terns, Michael P ^a   Terns, Rebecca M ^a  

^a University of Georgia   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0035975962     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(01)00517-6     Document Type: Review

References (19)

1. Identification and characterization of a spinal muscular atrophy-determining gene
2. SMN tudor domain structure and its interaction with the Sm proteins
3. The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1
4. A functional interaction between the survival motor neuron complex and RNA polymerase II
5. Direct interaction of the spinal muscular atrophy disease protein SMN with the small nucleolar RNA-associated protein fibrillarin
6. Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein
7. SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets
8. Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN)
9. Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: Implications for spinal muscular atrophy
10. The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis
11. The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins
12. Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins
13. A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs
14. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins
15. Guided tours: From precursor snoRNA to functional snoRNP
16. Small nucleolar RNAs: Versatile trans-acting molecules of ancient evolutionary origin
17. Residual Cajal bodies in coilin knockout mice fail to recruit Sm snRNPs and SMN, the spinal muscular atrophy gene product
18. A novel function for SMN, the spinal muscular atrophy disease gene product, in prem-RNA splicing
19. Cajal bodies: The first 100 years