spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bregman, D. B.
Right arrow Articles by Warren, S. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bregman, D. B.
Right arrow Articles by Warren, S. L.

Journal of Cell Science, Vol 107, Issue 3 387-396, Copyright © 1994 by Company of Biologists


JOURNAL ARTICLES

Cytostellin distributes to nuclear regions enriched with splicing factors

DB Bregman, L Du, Y Li, S Ribisi and SL Warren
Department of Pathology, Yale University School of Medicine, New Haven, CT 06510.

Cytostellin, a approximately 240 kDa phosphoprotein found in all cells examined from human to yeast, is predominantly intranuclear in interphase mammalian cells and undergoes continuous redistribution during the cell cycle. Here, mammalian cytostellin is shown to localize to intranuclear regions enriched with multiple splicing proteins, including spliceosome assembly factor, SC-35. Cytostellin and the splicing proteins also co-localize to discrete foci (called 'dots'), which are distributed throughout the cell during mitosis and part of G1. The cytostellin that is localized to these dots resists extraction by Triton X-100, indicating that it is tightly associated with insoluble cell structures. All immunostainable cytostellin reappears in the nucleus before S-phase. Although cytostellin and the splicing proteins co-localize in interphase and dividing cells, cytostellin is not detected in purified spliceosomes, and it associates with six unidentified proteins, forming a macromolecular complex that is biochemically distinct from the proteins that comprise spliceosomes. This macromolecular complex is detected at constant levels throughout the cell cycle, and the level of cytostellin protein remains constant during the cell cycle. Nevertheless, intranuclear cytostellin immunostaining fluctuates markedly during the cell cycle. The monoclonal antibody (mAb) H5 epitope of cytostellin is 'masked' in serum-starved cells, but 60 minutes after serum stimulation intense cytostellin immunoreactivity appears in the nuclear speckles. This rapid induction of cytostellin immunoreactivity in subnuclear regions enriched with many splicing factors, as well as accumulations of RNA polymerase II (Pol II) transcripts, suggests that cytostellin may have a function related to mRNA biogenesis.


This article has been cited by other articles:


Home page
J. Virol.Home page
K. A. Fraser and S. A. Rice
Herpes Simplex Virus Immediate-Early Protein ICP22 Triggers Loss of Serine 2-Phosphorylated RNA Polymerase II
J. Virol., May 15, 2007; 81(10): 5091 - 5101.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
S. Q. Xie, S. Martin, P. V. Guillot, D. L. Bentley, and A. Pombo
Splicing Speckles Are Not Reservoirs of RNA Polymerase II, but Contain an Inactive Form, Phosphorylated on Serine2 Residues of the C-Terminal Domain
Mol. Biol. Cell, April 1, 2006; 17(4): 1723 - 1733.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
K. V. Prasanth, P. A. Sacco-Bubulya, S. G. Prasanth, and D. L. Spector
Sequential Entry of Components of Gene Expression Machinery into Daughter Nuclei
Mol. Biol. Cell, March 1, 2003; 14(3): 1043 - 1057.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. S. Lin, M.-F. Dubois, and M. E. Dahmus
TFIIF-associating Carboxyl-terminal Domain Phosphatase Dephosphorylates Phosphoserines 2 and 5 of RNA Polymerase II
J. Biol. Chem., November 22, 2002; 277(48): 45949 - 45956.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
C. D. Kaplan, J. R. Morris, C.-t. Wu, and F. Winston
Spt5 and Spt6 are associated with active transcription and have characteristics of general elongation factors in D. melanogaster
Genes & Dev., October 15, 2000; 14(20): 2623 - 2634.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
M. Abdellatif, S. E. Packer, L. H. Michael, D. Zhang, M. J. Charng, and M. D. Schneider
A Ras-Dependent Pathway Regulates RNA Polymerase II Phosphorylation in Cardiac Myocytes: Implications for Cardiac Hypertrophy
Mol. Cell. Biol., November 1, 1998; 18(11): 6729 - 6736.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
M. Patturajan, X. Wei, R. Berezney, and J. L. Corden
A Nuclear Matrix Protein Interacts with the Phosphorylated C-Terminal Domain of RNA Polymerase II
Mol. Cell. Biol., April 1, 1998; 18(4): 2406 - 2415.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
M. Patturajan, R. J. Schulte, B. M. Sefton, R. Berezney, M. Vincent, O. Bensaude, S. L. Warren, and J. L. Corden
Growth-related Changes in Phosphorylation of Yeast RNA Polymerase II
J. Biol. Chem., February 20, 1998; 273(8): 4689 - 4694.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
B. Grondin, F. Cote, M. Bazinet, M. Vincent, and M. Aubry
Direct Interaction of the KRAB/Cys2-His2 Zinc Finger Protein ZNF74 with a Hyperphosphorylated Form of the RNA Polymerase II Largest Subunit
J. Biol. Chem., October 31, 1997; 272(44): 27877 - 27885.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
S Bisotto, P Lauriault, M Duval, and M Vincent
Colocalization of a high molecular mass phosphoprotein of the nuclear matrix (p255) with spliceosomes
J. Cell Sci., January 5, 1995; 108(5): 1873 - 1882.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
A. Beven, G. Simpson, J. Brown, and P. Shaw
The organization of spliceosomal components in the nuclei of higher plants
J. Cell Sci., January 2, 1995; 108(2): 509 - 518.
[Abstract] [PDF]




© The Company of Biologists Ltd 1994