The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway

Autor: Massenet S., Pellizzoni L., Paushkin S., Mattaj I.W., Dreyfuss G.

Publikováno v: Molecular and cellular biology
22 (2002): 6533–6541.
info:cnr-pdr/source/autori:Massenet S., Pellizzoni L., Paushkin S., Mattaj I.W. and Dreyfuss G./titolo:The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway/doi:/rivista:Molecular and cellular biology (Print)/anno:2002/pagina_da:6533/pagina_a:6541/intervallo_pagine:6533–6541/volume:22

The common neurodegenerative disease spinal muscular atrophy is caused by reduced levels of the survival of motor neurons (SMN) protein. SMN associates with several proteins (Gemin2 to Gemin6) to form a large complex which is found both in the cytopl

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An abundant U6 snRNP found in germ cells and embryos of Xenopus laevis.

Autor: Hamm, J., Mattaj, I.W.

Publikováno v: The EMBO Journal; December 1989, Vol. 8 Issue: 13 p4179-4187, 9p

TFIID is required for in vitro transcription of the human U6 gene by RNA polymerase III.

Autor: Simmen, K.A., Bernués, J., Parry, H.D., Stunnenberg, H.G., Berkenstam, A., Cavallini, B., Egly, J.M., Mattaj, I.W.

Publikováno v: The EMBO Journal; July 1991, Vol. 10 Issue: 7 p1853-1862, 10p

A complex secondary structure in U1A pre‐mRNA that binds two molecules of U1A protein is required for regulation of polyadenylation.

Autor: van Gelder, C.W., Gunderson, S.I., Jansen, E.J., Boelens, W.C., Polycarpou‐Schwarz, M., Mattaj, I.W., van Venrooij, W.J.

Publikováno v: The EMBO Journal; December 1993, Vol. 12 Issue: 13 p5191-5200, 10p