Literature DB >> 667064

Studies on the degradation of high mobility group non-histone chromosomal proteins.

G H Goodwin, J M Walker, E W Johns.   

Abstract

During the isolation of high mobility group non-histone proteins from calf thymus chromatin by methods described previously (e.g. Goodwin, G.H., Nicolas, R.H. and Johns, E.W. (1975) Biochim. Biophys, Acta. 405, 280--291) protein degradation occurs resulting in a number of proteins appearing in the chromatin extracts which are not present in high mobility group protein preparations in which proteolysis has been completely inhibited. These extra proteins, formerly numbered high mobility group proteins 3, 5, 6 and 8, are thus probably degradation products of other nuclear proteins, produced during the isolation procedure. From the amino acid analyses, tryptic peptides and N-terminal sequences, it is concluded that high mobility group protein 3 is probably a degradation product of high mobility group protein 1. The amino acid analysis of high mobility group protein 8 is very similar to that of the N-terminal half of histone H1 suggesting that high mobility group protein 8 is a degradation product of this histone.

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Year:  1978        PMID: 667064     DOI: 10.1016/0005-2787(78)90076-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  14 in total

1.  Chromosomal protein HMG-14 gene maps to the Down syndrome region of human chromosome 21 and is overexpressed in mouse trisomy 16.

Authors:  J Pash; N Popescu; M Matocha; S Rapoport; M Bustin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

2.  Evolution of high mobility group nucleosome-binding proteins and its implications for vertebrate chromatin specialization.

Authors:  Rodrigo González-Romero; José M Eirín-López; Juan Ausió
Journal:  Mol Biol Evol       Date:  2014-10-03       Impact factor: 16.240

3.  Does high-mobility-group non-histone protein HMG 1 interact specifically with histone H1 subfractions?

Authors:  P D Cary; K V Shooter; G H Goodwin; E W Johns; J Y Olayemi; P G Hartman; E M Bradbury
Journal:  Biochem J       Date:  1979-12-01       Impact factor: 3.857

4.  DNA looping by the HMG-box domains of HMG1 and modulation of DNA binding by the acidic C-terminal domain.

Authors:  M Stros; J Stokrová; J O Thomas
Journal:  Nucleic Acids Res       Date:  1994-03-25       Impact factor: 16.971

5.  Selective release of HMG nonhistone proteins during DNase digestion of Tetrahymena chromatin at different stages of the cell cycle.

Authors:  K Hamana; M Zama
Journal:  Nucleic Acids Res       Date:  1980-11-25       Impact factor: 16.971

6.  Loss of chromosomal high mobility group proteins HMG1 and HMG2 when mouse neuroblastoma and Friend erythroleukemia cells become committed to differentiation.

Authors:  S M Seyedin; J R Pehrson; R D Cole
Journal:  Proc Natl Acad Sci U S A       Date:  1981-10       Impact factor: 11.205

7.  Differential phosphorylation of nuclear nonhistone high mobility group proteins HMG 14 and HMG 17 during the cell cycle.

Authors:  J S Bhorjee
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

8.  The characterisation of 1SF monomer nucleosomes from hen oviduct and the partial characterisation of a third HMG14/17-like in such nucleosomes.

Authors:  G H Goodwin; C A Wright; E W Johns
Journal:  Nucleic Acids Res       Date:  1981-06-25       Impact factor: 16.971

9.  Analysis of putative high-mobility-group (HMG) proteins in neuronal and glial nuclei from rabbit brain.

Authors:  P Greenwood; J C Silver; I R Brown
Journal:  Neurochem Res       Date:  1981-06       Impact factor: 3.996

10.  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

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