Literature DB >> 7204499

Heterogeneous binding of high mobility group chromosomal proteins to nuclei.

J S Gordon, J Bruno, J J Lucas.   

Abstract

A dramatic difference is observed in the intracellular distribution of the high mobility group (HMG) proteins when chicken embryo fibroblasts are fractionated into nucleus and cytoplasm by either mass enucleation of cytochalasin-B-treated cells or by differential centrifugation of mechanically disrupted cells. Nuclei (karyoplasts) obtained by cytochalasin B treatment of cells contain more than 90 percent of the HMG 1, while enucleated cytoplasts contain the remainder. A similar distribution between karyoplasts and cytoplasts is observed for the H1 histones and the nucleosomal core histones as anticipated. The presence of these proteins, in low amounts, in the cytoplast preparation can be accounted for by the small percentage of unenucleated cells present. In contrast, the nuclei isolated from mechanically disrupted cells contain only 30-40 percent of the total HMGs 1 and 2, the remainder being recovered in the cytosol fraction. No histone is observed in the cytosol fraction. Unike the higher molecular weight HMGs, most of the HMGs 14 and 17 sediment with the nuclei after cell lysis by mechanical disruption. The distribution of HMGs is unaffected by incubating cells with cytochalasin B and mechanically fractionating rather than enucleating them. Therefore, the dramatic difference in HMG 1 distribution observed using the two fractionation techniques cannot be explained by a cytochalasin-B-induced redistribution. On reextraction and sedimentation of isolated nuclei obtained by mechanical cell disruption, only 8 percent of the HMG 1 is released to the supernate. Thus, the majority of the HMG 1 originally isolated with these nuclei, representing 35 percent of the total HMG 1, is stably bound, as is all the HMGs 14 and 17. The remaining 65 percent of the HMGs 1 and 2 is unstably bound and leaks to the cytosol fraction under the conditions of mechanical disruption. It is suggested that the unstably bound HMGs form a protein pool capable of equilibrating between cytoplasm and stably bound HMGs.

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Year:  1981        PMID: 7204499      PMCID: PMC2111745          DOI: 10.1083/jcb.88.2.373

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  35 in total

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Authors:  G Herrick; B B Spear; G Veomett
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2.  Isolation of skeletal muscle nuclei.

Authors:  L Kuehl
Journal:  Exp Cell Res       Date:  1975-03-15       Impact factor: 3.905

3.  The construction of viable nuclear-cytoplasmic hybrid cells by nuclear transplantation.

Authors:  J J Lucas; J R Kates
Journal:  Cell       Date:  1976-03       Impact factor: 41.582

4.  The regeneration and division of mouse L-cell karyoplasts.

Authors:  J J Lucas; E Szekely; J R Kates
Journal:  Cell       Date:  1976-01       Impact factor: 41.582

5.  Non-histone chromosomal proteins from HeLa cells. A survey by high resolution, two-dimensional electrophoresis.

Authors:  J L Peterson; E H McConkey
Journal:  J Biol Chem       Date:  1976-01-25       Impact factor: 5.157

6.  Stoichiometry of chromatin proteins.

Authors:  W T Garrard; W R Pearson; S K Wake; J Bonner
Journal:  Biochem Biophys Res Commun       Date:  1974-05-07       Impact factor: 3.575

7.  An electrophoretic comparison of vertebrate histones.

Authors:  S Panyim; D Bilek; R Chalkley
Journal:  J Biol Chem       Date:  1971-07-10       Impact factor: 5.157

8.  A new histone from trout testis.

Authors:  D T Wigle; G H Dixon
Journal:  J Biol Chem       Date:  1971-09-25       Impact factor: 5.157

9.  Enucleation of mammalian cells with cytochalasin B.

Authors:  D M Prescott; D Myerson; J Wallace
Journal:  Exp Cell Res       Date:  1972       Impact factor: 3.905

10.  Specific nucleolar and nucleoplasmic RNA polymerases.

Authors:  R G Roeder; W J Rutter
Journal:  Proc Natl Acad Sci U S A       Date:  1970-03       Impact factor: 11.205

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  10 in total

1.  Activation of inflammasomes requires intracellular redistribution of the apoptotic speck-like protein containing a caspase recruitment domain.

Authors:  Nicole B Bryan; Andrea Dorfleutner; Yon Rojanasakul; Christian Stehlik
Journal:  J Immunol       Date:  2009-03-01       Impact factor: 5.422

2.  Influence of nonhistone chromatin protein HMG-1 on the enzymatic digestion of purified DNA.

Authors:  K Shastri; P J Isackson; J L Fishback; M D Land; G R Reeck
Journal:  Nucleic Acids Res       Date:  1982-08-25       Impact factor: 16.971

3.  Heterogeneity of high-mobility-group protein 2. Enrichment of a rapidly migrating form in testis.

Authors:  L R Bucci; W A Brock; M L Meistrich
Journal:  Biochem J       Date:  1985-07-01       Impact factor: 3.857

4.  Nuclear localization of p85s6k: functional requirement for entry into S phase.

Authors:  C Reinhard; A Fernandez; N J Lamb; G Thomas
Journal:  EMBO J       Date:  1994-04-01       Impact factor: 11.598

5.  Concentrations of high-mobility-group proteins in the nucleus and cytoplasm of several rat tissues.

Authors:  L Kuehl; B Salmond; L Tran
Journal:  J Cell Biol       Date:  1984-08       Impact factor: 10.539

6.  Phosphorylation on protein kinase C sites inhibits nuclear import of lamin B2.

Authors:  H Hennekes; M Peter; K Weber; E A Nigg
Journal:  J Cell Biol       Date:  1993-03       Impact factor: 10.539

7.  Casein kinase II is a predominantly nuclear enzyme.

Authors:  W Krek; G Maridor; E A Nigg
Journal:  J Cell Biol       Date:  1992-01       Impact factor: 10.539

8.  Comparative studies on microinjected high-mobility-group chromosomal proteins, HMG1 and HMG2.

Authors:  L Wu; M Rechsteiner; L Kuehl
Journal:  J Cell Biol       Date:  1981-11       Impact factor: 10.539

9.  High mobility group proteins of amphibian oocytes: a large storage pool of a soluble high mobility group-1-like protein and involvement in transcriptional events.

Authors:  J A Kleinschmidt; U Scheer; M C Dabauvalle; M Bustin; W W Franke
Journal:  J Cell Biol       Date:  1983-09       Impact factor: 10.539

10.  Cell cycle analysis of the activity, subcellular localization, and subunit composition of human CAK (CDK-activating kinase).

Authors:  J P Tassan; S J Schultz; J Bartek; E A Nigg
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

  10 in total

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