Literature DB >> 3527729

Redistribution of the nuclear mitotic apparatus protein (NuMA) during mitosis and nuclear assembly. Properties of purified NuMA protein.

C M Price, D E Pettijohn.   

Abstract

Monoclonal antibodies and human autoimmune sera specific for the nuclear mitotic apparatus protein (NuMA protein) were applied to study the structure of this protein and its intracellular distribution. The NuMA protein was purified using immuno-affinity columns. Studies on this large (250 kD) nuclear protein indicated that it is a highly asymmetric phosphoprotein. It is present in all mammalian cells examined and in those of some non-mammals. Immunofluorescence studies on fixed cells demonstrated that its intracellular distribution is essentially the same in all species at all stages of the cell cycle. Immunoblot (western blot) analysis showed that the size of the NuMA protein varies slightly in different species. At the onset of mitosis the NuMA protein redistributes from the nucleus to two centrosomal structures that later will become part of the mitotic spindle pole. This occurs at the time of nuclear breakdown and eventually leads to an accumulation of the NuMA protein at the polar region of the mitotic spindle. After anaphase the protein redistributes from the spindle polar region into the reforming nucleus and concentrates initially at the site where nuclear lamins and perichomatin have been reported to assemble. Living cells microinjected with fluorescent anti-NuMA antibodies were studied to examine parameters that effect the redistribution of the NuMA protein in vivo. These experiments indicate that microtubule assembly is essential for the NuMA protein to accumulate in the polar region.

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Year:  1986        PMID: 3527729     DOI: 10.1016/0014-4827(86)90478-7

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  20 in total

1.  The nuclear-mitotic apparatus protein is important in the establishment and maintenance of the bipolar mitotic spindle apparatus.

Authors:  C H Yang; M Snyder
Journal:  Mol Biol Cell       Date:  1992-11       Impact factor: 4.138

2.  Inhibition of protein 4.1 R and NuMA interaction by mutagenization of their binding-sites abrogates nuclear localization of 4.1 R.

Authors:  Subhendra N Mattagajasingh; Shu-Ching Huang; Edward J Benz
Journal:  Clin Transl Sci       Date:  2009-04       Impact factor: 4.689

3.  Protein 4.1N binding to nuclear mitotic apparatus protein in PC12 cells mediates the antiproliferative actions of nerve growth factor.

Authors:  K Ye; D A Compton; M M Lai; L D Walensky; S H Snyder
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

4.  Asymmetric cell divisions promote stratification and differentiation of mammalian skin.

Authors:  Terry Lechler; Elaine Fuchs
Journal:  Nature       Date:  2005-08-10       Impact factor: 49.962

5.  Introduction of proteins into living bacterial cells: distribution of labeled HU protein in Escherichia coli.

Authors:  V L Shellman; D E Pettijohn
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

6.  Mitotic regulation of protein 4.1R involves phosphorylation by cdc2 kinase.

Authors:  Shu-Ching Huang; Eva S Liu; Siu-Hong Chan; Indira D Munagala; Heidi T Cho; Ramasamy Jagadeeswaran; Edward J Benz
Journal:  Mol Biol Cell       Date:  2004-11-03       Impact factor: 4.138

Review 7.  NuMA after 30 years: the matrix revisited.

Authors:  Andreea E Radulescu; Don W Cleveland
Journal:  Trends Cell Biol       Date:  2010-04       Impact factor: 20.808

8.  Tumorigenic human squamous lung cancer cells have defined cell surface carbohydrates that are absent from nontumorigenic cells.

Authors:  D E Pettijohn; O Pfenninger; J Brown; R Duke; L Olsson
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

9.  NuMA is required for proper spindle assembly and chromosome alignment in prometaphase.

Authors:  Laurence Haren; Nicole Gnadt; Michel Wright; Andreas Merdes
Journal:  BMC Res Notes       Date:  2009-04-28

10.  Autoantibody to NA14 is an independent marker primarily for Sjogren's syndrome.

Authors:  Kazuhisa Nozawa; Keigo Ikeda; Minoru Satoh; Westley H Reeves; Carol M Stewart; Yueh-Chun Li; Tim J Yen; Rosa M Rios; Kenji Takamori; Hideoki Ogawa; Iwao Sekigawa; Yoshinari Takasaki; Edward K L Chan
Journal:  Front Biosci (Landmark Ed)       Date:  2009-01-01
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