Literature DB >> 476514

Identification of nonhistone chromatin proteins in chromatin subunits (or mononucleosomes) devoid of histone H1.

P K Chan, C C Liew.   

Abstract

Rat liver chromatin was digested by micrococcal nuclease. Chromatin subunits (or mononucleosomes) were isolated by sucrose density gradient and subsequently fractionated by 6% polyacrylamide gel electrophoresis into two major components. One component (MN1) of the mononucleosomes had a higher mobility, contained histones H2A, H2B, H3, H4, and shorter DNA fragments (140 base pairs) while the other (MN2) contained all five histones and longer DNA fragments (180 base pairs). Both submononucleosomes (MN1 and MN2) were found to contain nonhistone chromatin proteins (NHCP). By electrophoresis in 15% sodium dodecyl sulfate-polyacrylamide gel, 9 and 11 major fractions of NHCP were identified in the submononucleosomes MN1 and MN2, respectively. It was also observed that treatment of mononucleosomes with 0.6 M NaCl removes most of these NHCP and histone H1 except for two major NHCP which remain in the core particles.

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Year:  1979        PMID: 476514     DOI: 10.1139/o79-084

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  2 in total

1.  Identification of a phosphoprotein in the nuclear matrix by monoclonal antibodies.

Authors:  M J Halikowski; C C Liew
Journal:  Biochem J       Date:  1987-02-01       Impact factor: 3.857

2.  A chromosomal phosphoprotein is preferentially released by mild micrococcal-nuclease digestion.

Authors:  C C Liew; M J Halikowski; M S Zhao
Journal:  Biochem J       Date:  1984-06-01       Impact factor: 3.857

  2 in total

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