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The phosphorylation of high mobility group proteins 14 and 17 and their distribution in chromatin.

Abstract
The phosphorylation of the high mobility group (HMG) proteins has been investigated in mouse Ehrlich ascites, L1210 and P388 leukemia cells, human colon carcinoma cells (HT-29), and Chinese hamster ovary cells. HMG 14 and 17, but not HMB 1 and 2, were phosphorylated in the nuclei of all cell lines with a serine being the site of modification for both proteins in Ehrlich ascites cells. Phosphorylation of HMG 14 and 17 was greatly reduced in cultured cells at plateau phase in comparison to log phase cells, suggesting that modification of HMG 14 and 17 is growth-associated. However, phosphorylation was not linked to DNA synthesis, since incorporation of 32P did not vary through G1 and S phase in synchronized Chinese hamster ovary cells. Treatment of HT-29 or Ehrlich ascites cells with sodium butyrate reduced HMG phosphorylation by 30 and 70%, respectively. The distribution of the phosphorylated HMG proteins in chromatin was examined using micrococcal nuclease and DNase I. 32P-HMG 14 and 17 were preferentially associated with micrococcal nuclease-sensitive regions as demonstrated by the release of a substantial fraction of the phosphorylated forms of these proteins under conditions which solubilized less than 3% of the DNA. Short digestions with DNase I did not show a marked release of 32P-HMG 14 or 17.
AuthorsJ D Saffer, R I Glazer
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 257 Issue 8 Pg. 4655-60 (Apr 25 1982) ISSN: 0021-9258 [Print] UNITED STATES
PMID6461658 (Publication Type: Journal Article)
Chemical References
  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • High Mobility Group Proteins
  • Histones
Topics
  • Animals
  • Carcinoma, Ehrlich Tumor (metabolism)
  • Cell Line
  • Chromatin (metabolism)
  • Chromosomal Proteins, Non-Histone (metabolism)
  • Colonic Neoplasms (metabolism)
  • Cricetinae
  • Cricetulus
  • Female
  • High Mobility Group Proteins
  • Histones (metabolism)
  • Humans
  • Kinetics
  • Leukemia L1210 (metabolism)
  • Leukemia P388 (metabolism)
  • Mice
  • Ovary
  • Phosphorylation

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