Literature DB >> 1478941

Cytostellin: a novel, highly conserved protein that undergoes continuous redistribution during the cell cycle.

S L Warren1, A S Landolfi, C Curtis, J S Morrow.   

Abstract

Cytostellin, a 240 kDa protein, has been purified from mammalian cells by immunoaffinity chromatography using monoclonal antibody H5. Immunofluorescence microscopy shows diffuse and punctate cytostellin immunoreactivity in interphase nuclei. Nuclease digestion and salt extraction are not required to expose the epitope. The onset of prophase is marked by the appearance of multiple intensely immunofluorescent cytostellin-containing 'bodies' within the nucleus. Nuclear disassembly is heralded by the movement of cytostellin bodies from the nucleus to multiple positions throughout the cell. Cytostellin bodies in metaphase, anaphase and telophase cells are widely dispersed, including some in cell processes far removed from the mitotic spindle apparatus. However, a distinct subset of larger, more intensely staining bodies surrounds the mitotic spindle apparatus. Cytostellin bodies remain in the cytoplasm of the daughter cells and disappear after the appearance of nascent nuclei. Cytostellin is immunologically distinct from other nuclear and cytoplasmic proteins, and it has been detected by immunoblot analysis in all species tested from yeast to humans. Based upon these findings, we postulate that cytostellin has a cell cycle-dependent function which is conserved in higher and lower eukaryotic cells.

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Year:  1992        PMID: 1478941     DOI: 10.1242/jcs.103.2.381

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  29 in total

1.  Subnuclear localization and Cajal body targeting of transcription elongation factor TFIIS in amphibian oocytes.

Authors:  Abigail J Smith; Yan Ling; Garry T Morgan
Journal:  Mol Biol Cell       Date:  2003-03       Impact factor: 4.138

2.  Subnuclear targeting of the RNA-binding motif protein RBM6 to splicing speckles and nascent transcripts.

Authors:  Emma Heath; Fred Sablitzky; Garry T Morgan
Journal:  Chromosome Res       Date:  2010-11-18       Impact factor: 5.239

3.  Dynamic Behavior of the RNA Polymerase II and the Ubiquitin Proteasome System During the Neuronal DNA Damage Response to Ionizing Radiation.

Authors:  Iñigo Casafont; Ana Palanca; Vanesa Lafarga; Jorge Mata-Garrido; Maria T Berciano; Miguel Lafarga
Journal:  Mol Neurobiol       Date:  2015-12-11       Impact factor: 5.590

4.  Nuclear translocation and carboxyl-terminal domain phosphorylation of RNA polymerase II delineate the two phases of zygotic gene activation in mammalian embryos.

Authors:  S Bellier; S Chastant; P Adenot; M Vincent; J P Renard; O Bensaude
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

5.  The nuclear matrix protein p255 is a highly phosphorylated form of RNA polymerase II largest subunit which associates with spliceosomes.

Authors:  M Vincent; P Lauriault; M F Dubois; S Lavoie; O Bensaude; B Chabot
Journal:  Nucleic Acids Res       Date:  1996-12-01       Impact factor: 16.971

6.  A serine/arginine-rich nuclear matrix cyclophilin interacts with the C-terminal domain of RNA polymerase II.

Authors:  J P Bourquin; I Stagljar; P Meier; P Moosmann; J Silke; T Baechi; O Georgiev; W Schaffner
Journal:  Nucleic Acids Res       Date:  1997-06-01       Impact factor: 16.971

7.  PIE-1 is a bifunctional protein that regulates maternal and zygotic gene expression in the embryonic germ line of Caenorhabditis elegans.

Authors:  C Tenenhaus; K Subramaniam; M A Dunn; G Seydoux
Journal:  Genes Dev       Date:  2001-04-15       Impact factor: 11.361

8.  Yeast Swd2 is essential because of antagonism between Set1 histone methyltransferase complex and APT (associated with Pta1) termination factor.

Authors:  Luis M Soares; Stephen Buratowski
Journal:  J Biol Chem       Date:  2012-03-19       Impact factor: 5.157

9.  Genetic interactions of Spt4-Spt5 and TFIIS with the RNA polymerase II CTD and CTD modifying enzymes in Saccharomyces cerevisiae.

Authors:  D L Lindstrom; G A Hartzog
Journal:  Genetics       Date:  2001-10       Impact factor: 4.562

10.  Inactive X chromosome-specific histone H3 modifications and CpG hypomethylation flank a chromatin boundary between an X-inactivated and an escape gene.

Authors:  Yuji Goto; Hiroshi Kimura
Journal:  Nucleic Acids Res       Date:  2009-12       Impact factor: 16.971

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