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Nature Cell Biology (297)
References
44
Referenced
96
-
Munsat, T. L. & Davies, K. E., eds International SMA consortium meeting, 26–28 June 1992, Bonn, Germany. Neuromuscul Disord. 2, 423–428 (1992).
(
10.1016/S0960-8966(06)80015-5
) / Neuromuscul Disord. by TL Munsat (1992) -
Wirth, B. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Hum. Mutat. 15, 228–237 (2000).
(
10.1002/(SICI)1098-1004(200003)15:3<228::AID-HUMU3>3.0.CO;2-9
) / Hum. Mutat. by B Wirth (2000) -
Lefebvre, S. et al. Identification and characterization of a spinal muscular atrophy- determining gene. Cell 80, 155–165 (1995).
(
10.1016/0092-8674(95)90460-3
) / Cell by S Lefebvre (1995) -
Schrank, B. et al. Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos. Proc. Natl Acad. Sci. USA 94, 9920–9925 (1997).
(
10.1073/pnas.94.18.9920
) / Proc. Natl Acad. Sci. USA by B Schrank (1997) -
Miguel-Aliaga, I. et al. 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 (1999).
(
10.1093/hmg/8.12.2133
) / Hum. Mol. Genet. by I Miguel-Aliaga (1999) -
Monani, U. R. et al. A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. Hum. Mol. Genet. 8, 1177–1183 (1999).
(
10.1093/hmg/8.7.1177
) / Hum. Mol. Genet. by UR Monani (1999) -
Lorson, C. L., Hahnen, E., Androphy, E. J. & Wirth, B. A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl Acad. Sci. USA 96, 6307–6311 (1999).
(
10.1073/pnas.96.11.6307
) / Proc. Natl Acad. Sci. USA by CL Lorson (1999) -
Frugier, T. et al. Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy. Hum. Mol. Genet. 9, 849–858 (2000).
(
10.1093/hmg/9.5.849
) / Hum. Mol. Genet. by T Frugier (2000) -
Hsieh-Li, H. M. et al. A mouse model for spinal muscular atrophy. Nature Genet. 24, 66–70 (2000).
(
10.1038/71709
) / Nature Genet. by HM Hsieh-Li (2000) -
Monani, U. R. et al. The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn−/− mice and results in a mouse with spinal muscular atrophy. Hum. Mol. Genet. 9, 333–339 (2000).
(
10.1093/hmg/9.3.333
) / Hum. Mol. Genet. by U Monani (2000) -
Liu, Q. & Dreyfuss, G. A novel nuclear structure containing the survival of motor neurons protein. EMBO J. 15, 3555–3565 (1996).
(
10.1002/j.1460-2075.1996.tb00725.x
) / EMBO J. by Q Liu (1996) -
Matera, A. G. & Frey, M. R. Coiled bodies and gems: Janus or gemini? Am. J. Hum. Genet. 63, 317–321 (1998).
(
10.1086/301992
) / Am. J. Hum. Genet. by AG Matera (1998) -
Carvalho, T. et al. The spinal muscular atrophy disease gene product, SMN: A link between snRNP biogenesis and the Cajal (coiled) body. J. Cell Biol. 147, 715–728 (1999).
(
10.1083/jcb.147.4.715
) / J. Cell Biol. by T Carvalho (1999) -
Young, P. J., Le, T. T., thi Man, N., Burghes, A. H. & Morris, G. E. 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 (2000).
(
10.1006/excr.2000.4858
) / Exp. Cell Res. by PJ Young (2000) -
Liu, Q., Fischer, U., Wang, F. & Dreyfuss, G. The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1, are in a complex with spliceosomal snRNP proteins. Cell 90, 1013–1021 (1997).
(
10.1016/S0092-8674(00)80367-0
) / Cell by Q Liu (1997) -
Fischer, U., Liu, Q. & Dreyfuss, G. The SMN–SIP1 complex has an essential role in spliceosomal snRNP biogenesis. Cell 90, 1023–1029 (1997).
(
10.1016/S0092-8674(00)80368-2
) / Cell by U Fischer (1997) -
Pellizzoni, L., Kataoka, N., Charroux, B. & Dreyfuss, G. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing. Cell 95, 615–624 (1998).
(
10.1016/S0092-8674(00)81632-3
) / Cell by L Pellizzoni (1998) -
Pagliardini, S. et al. Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord. Hum. Mol. Genet. 9, 47–56 (2000).
(
10.1093/hmg/9.1.47
) / Hum. Mol. Genet. by S Pagliardini (2000) -
Coovert, D. D. et al. The survival motor neuron protein in spinal muscular atrophy. Hum. Mol. Genet. 6, 1205–1214 (1997).
(
10.1093/hmg/6.8.1205
) / Hum. Mol. Genet. by DD Coovert (1997) -
Lefebvre, S. et al. Correlation between severity and SMN protein level in spinal muscular atrophy. Nature Genet. 16, 265–269 (1997).
(
10.1038/ng0797-265
) / Nature Genet. by S Lefebvre (1997) -
Galcheva-Gargova, Z. et al. Binding of zinc-finger protein ZPR1 to the epidermal growth factor receptor. Science 272, 1797–1802 (1996).
(
10.1126/science.272.5269.1797
) / Science by Z Galcheva-Gargova (1996) -
Galcheva-Gargova, Z. et al. The cytoplasmic zinc-finger protein ZPR1 accumulates in the nucleolus of proliferating cells. Mol. Biol. Cell 9, 2963–2971 (1998).
(
10.1091/mbc.9.10.2963
) / Mol. Biol. Cell by Z Galcheva-Gargova (1998) -
Gangwani, L., Mikrut, M., Galcheva-Gargova, Z. & Davis, R. J. Interaction of ZPR1 with translation elongation factor-1α in proliferating cells. J. Cell Biol. 143, 1471–1484 (1998).
(
10.1083/jcb.143.6.1471
) / J. Cell Biol. by L Gangwani (1998) -
Adams, M. D. et al. The genome sequence of Drosophila melanogaster. Science 287, 2185–2195 (2000).
(
10.1126/science.287.5461.2185
) / Science by M Adams (2000) -
The C. elegans sequencing consortium. Genome sequence of the nematode C. elegans: a platform for investigating biology. Science 282, 2012–2018 (1998).
(
10.1126/science.282.5396.2012
) -
Bertrandy, S. et al. The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution. Hum. Mol. Genet. 8, 775–782 (1999).
(
10.1093/hmg/8.5.775
) / Hum. Mol. Genet. by S Bertrandy (1999) -
Owen, N., Doe, C. L., Mellor, J. & Davies, K. E. Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein. Hum. Mol. Genet. 9, 675–684 (2000).
(
10.1093/hmg/9.5.675
) / Hum. Mol. Genet. by N Owen (2000) -
Charroux, B. et al. Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems. J. Cell Biol. 147, 1181–1194 (1999).
(
10.1083/jcb.147.6.1181
) / J. Cell Biol. by B Charroux (1999) -
Lorson, C. L. et al. SMN oligomerization defect correlates with spinal muscular atrophy severity. Nature Genet. 19, 63–66 (1998).
(
10.1038/ng0598-63
) / Nature Genet. by CL Lorson (1998) -
Charroux, B. et al. Gemin4. A novel component of the smn complex that is found in both gems and nucleoli. J. Cell Biol. 148, 1177–1186 (2000).
(
10.1083/jcb.148.6.1177
) / J. Cell Biol. by B Charroux (2000) -
Iwahashi, H. et al. Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy. Nature 390, 413–417 (1997).
(
10.1038/37144
) / Nature by H Iwahashi (1997) -
Strasswimmer, J. et al. Identification of survival motor neuron as a transcriptional activator- binding protein. Hum. Mol. Genet. 8, 1219–1226 (1999).
(
10.1093/hmg/8.7.1219
) / Hum. Mol. Genet. by J Strasswimmer (1999) -
Williams, B. Y., Hamilton, S. L. & Sarkar, H. K. The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain. FEBS Lett. 470, 207–210 (2000).
(
10.1016/S0014-5793(00)01320-X
) / FEBS Lett. by BY Williams (2000) -
Giesemann, T. et al. A role for polyproline motifs in the spinal muscular atrophy protein SMN. Profilins bind to and colocalize with smn in nuclear gems. J. Biol. Chem. 274, 37908–37914 (1999).
(
10.1074/jbc.274.53.37908
) / J. Biol. Chem. by T Giesemann (1999) -
Coovert, D. D. et al. Does the survival motor neuron protein (SMN) interact with Bcl-2? J. Med. Genet. 37, 536–539 (2000).
(
10.1136/jmg.37.7.536
) / J. Med. Genet. by DD Coovert (2000) -
Meister, G. et al. Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins. Hum. Mol. Genet. 9, 1977–1986 (2000).
(
10.1093/hmg/9.13.1977
) / Hum. Mol. Genet. by G Meister (2000) -
Pellizzoni, L., Charroux, B. & Dreyfuss, G. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. Proc. Natl Acad. Sci. USA 96, 11167–11172 (1999).
(
10.1073/pnas.96.20.11167
) / Proc. Natl Acad. Sci. USA by L Pellizzoni (1999) -
Gall, J. G., Bellini, M., Wu, Z. & Murphy, C. Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes. Mol. Biol. Cell 10, 4385–4402 (1999).
(
10.1091/mbc.10.12.4385
) / Mol. Biol. Cell by JG Gall (1999) -
Lewis, J. D. & Tollervey, D. Like attracts like: getting RNA processing together in the nucleus. Science 288, 1385–1389 (2000).
(
10.1126/science.288.5470.1385
) / Science by JD Lewis (2000) -
Sleeman, J. E. & Lamond, A. I. Nuclear organization of pre-mRNA splicing factors. Curr. Opin. Cell Biol. 11, 372–377 (1999).
(
10.1016/S0955-0674(99)80052-0
) / Curr. Opin. Cell Biol. by JE Sleeman (1999) -
Francis, J. W., Sandrock, A. W., Bhide, P. G., Vonsattel, J. P. & Brown, R. H. Jr Heterogeneity of subcellular localization and electrophoretic mobility of survival motor neuron (SMN) protein in mammalian neural cells and tissues. Proc. Natl Acad. Sci. USA 95, 6492–6497 (1998).
(
10.1073/pnas.95.11.6492
) / Proc. Natl Acad. Sci. USA by JW Francis (1998) - Harlow, E. & Lane, D. Antibodies: A Laboratory Manual, (Cold Spring Harbor Press, Cold Spring Harbor, 1988). / Antibodies: A Laboratory Manual by E Harlow (1988)
-
Andrade, L. E., Tan, E. M. & Chan, E. K. Immunocytochemical analysis of the coiled body in the cell cycle and during cell proliferation. Proc. Natl Acad. Sci. USA 90, 1947–1951 (1993).
(
10.1073/pnas.90.5.1947
) / Proc. Natl Acad. Sci. USA by LE Andrade (1993) -
Zillmann, M., Zapp, M. L. & Berget, S. M. Gel electrophoretic isolation of splicing complexes containing U1 small nuclear ribonucleoprotein particles. Mol. Cell. Biol. 8, 814–821 (1988).
(
10.1128/MCB.8.2.814
) / Mol. Cell. Biol. by M Zillmann (1988)
Dates
Type | When |
---|---|
Created | 22 years, 11 months ago (Sept. 20, 2002, 3:42 p.m.) |
Deposited | 2 years, 3 months ago (May 18, 2023, 4:03 p.m.) |
Indexed | 11 months ago (Sept. 20, 2024, 11:11 a.m.) |
Issued | 24 years, 5 months ago (March 9, 2001) |
Published | 24 years, 5 months ago (March 9, 2001) |
Published Online | 24 years, 5 months ago (March 9, 2001) |
Published Print | 24 years, 4 months ago (April 1, 2001) |
@article{Gangwani_2001, title={Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein}, volume={3}, ISSN={1476-4679}, url={http://dx.doi.org/10.1038/35070059}, DOI={10.1038/35070059}, number={4}, journal={Nature Cell Biology}, publisher={Springer Science and Business Media LLC}, author={Gangwani, Laxman and Mikrut, Monique and Theroux, Steven and Sharma, Manoj and Davis, Roger J.}, year={2001}, month=mar, pages={376–383} }