Erratum: Modulation of SMN nuclear foci and cytoplasmic localization by its C-terminus (Cellular and molecular Life Sciences (October 2004) 61:19-20 (2658-2663) DOI: 10.1007/s00018-004-4300-z);Modulation of SMN nuclear foci and cytoplasmic localization by its C-terminus

Cellular and Molecular Life Sciences

Volumn 61, Issue 19-20, 2004, Pages 2658-2663

  Hua, Y ^a   Zhou, J ^a  

^a UNIVERSITY OF MASSACHUSETTS   (United States)

Author keywords

SMN; Spinal muscular atrophy; Survival motor neuron; Tudor domain; Y G motif

Indexed keywords

AMINO ACID; GENE PRODUCT; SURVIVAL MOTOR NEURON PROTEIN;

AMINO ACID SEQUENCE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; CYTOPLASM; EXON; GENE LOCATION; NONHUMAN; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN MOTIF; REVIEW; SPINAL MUSCULAR ATROPHY;

EID: 9744267538     PISSN: 1420682X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00018-004-4100-5     Document Type: Erratum

References (24)

1. Lefebvre S., Burglen L, Reboullet S., Clermont O., Burlet P., Viollet L. et al. (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80: 155-165.
2. Buhler D., Raker V., Luhrmann R. and Fischer U. (1999) Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy. Hum. Mol. Genet. 8: 2351-2357
3. Fischer U., Liu Q. and Dreyfuss G. (1997) The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis. Cell 90: 1023-1029
4. Pellizzoni L., Yong J. and Dreyfuss G. (2002) Essential role for the SMN complex in the specificity of snRNP assembly. Science. 298: 1775-1779
5. Pellizzoni L., Kataoka N., Charroux B. and Dreyfuss G. (1998) A novel function for SMN, the spinal muscular atrophy disease gene product, inpre-mRNA splicing. Cell 95: 615-624
6. Pellizzoni L., Charroux B., Rappsilber J., Mann M. and Dreyfuss G. (2001) A functional interaction between the survival motor neuron complex and RNA polymerase II. J. Cell Biol. 152: 75-85
7. Williams B. Y., Hamilton S. L. and Sarkar H. K. (2000) The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain. FEBS Lett. 470: 207-210
8. Zou J., Barahmand-Pour F., Blackburn M. E., Matsui Y., Chansky H. A. and Yang E. (2004) Survival of motor neuron protein SMN interacts with transcription corepressor mSin3A. J. Biol. Chem. 279: 14922-14928
9. Kerr D. A., Nery J. P., Traystman R. J., Chau B. N. and Hardwick J. M. (2000) Survival motor neuron protein modulates neuron-specific apoptosis. Proc. Natl. Acad. Sci. USA 97: 13312-13317
10. Vyas S., Bechade C., Riveau B., Downward J. and Triller A. (2002) Involvement of survival motor neuron (SMN) protein in cell death. Hum. Mol. Genet. 11: 2751-2764
11. Ilangovan R., Marshall W. E., Hua Y. and Zhou J. (2003) Inhibition of apoptosis by Z-VAD-fmk in SMN-depleted S2 cells. J. Biol. Chem. 278: 30993-30999
12. Liu Q. and Dreyfuss G. (1996) A novel nuclear structure containing the survival of motor neurons protein. EMBO J. 15: 3555-3565
13. Young P. J., Le T. T., thi Man N., Burghes A. H. and Morris G. E. (2000) The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells. Exp. Cell Res. 256: 365-374
14. Paushkin S., Charroux B., Abel L., Perkinson R. A., Pellizzoni L. and Dreyfuss G. (2000) The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms. J. Biol. Chem. 275: 23841-23846
15. Miguel-Aliaga I., Culetto E., Walker D. S., Baylis H. A., Sattelle D. B. and Davies K. E. (1999) The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Hum. Mol. Genet. 8: 2133-2143
16. Hua Y. and Zhou J. (2004) Rpp20 interacts with SMN and is redistributed into SMN granules in response to stress. Biochem. Biophys. Res. Commun. 314: 268-276
17. Ogino S. and Wilson R. B. (2002) Genetic testing and risk assessment for spinal muscular atrophy (SMA). Hum. Genet. 111: 477-500
18. Zhang H. L., Pan F., Hong D., Shenoy S. M., Singer R. H. and Bassell G. J. (2003) Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization. J. Neurosci. 23: 6627-6637
19. Hua Y. and Zhou J. (2004) Survival motor neuron protein facilitates assembly of Stress Granules. FEBS Lett. 572: 69-74
20. Pellizzoni E., Baccon J., Charroux B. and Dreyfuss G. (2001) The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1. Curr. Biol. 11: 1079-1088
21. Rossoll W., Jablonka S., Andreassi C., Kroning A. K., Karle K., Monani U. R. et al. (2003) Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons. J. Cell Biol. 163: 801-812
22. Wilschanski M., Yahav Y., Yaacov Y, Blau H., Bentur L., Rivlin J. et al. (2003) Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations. N. Engl. J. Med. 349: 1433-1441
23. Howard M. T., Shirts B. H., Petros E. M., Flanigan K. M., Gesteland R. F. and Atkins J. F. (2000) Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy. Ann. Neurol. 48: 164-169
24. Keeling K. M., Brooks D. A., Hopwood J. J., Li P., Thompson J. N. and Bedwell D. M. (2001) Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of alpha-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation. Hum. Mol. Genet. 10: 291-299