Identification of a novel nuclear protein synthesized in growth-arrested human hepatoblastoma HepG2 cells

Eur J Biochem. 1991 Feb 14;195(3):723-9. doi: 10.1111/j.1432-1033.1991.tb15759.x.

Abstract

DNA synthesis of human hepatoblastoma HepG2 cells is reversibly inhibited by butyrate. When butyrate is removed from the culture medium, cells re-enter the cell cycle, synthesizing DNA with a time lag of about 12 h. HepG2 cells, growth-inhibited for 30 h with butyrate, synthesize and accumulate a nuclear protein, called D. Protein D synthesis is inhibited in cells which, released from the butyrate block, have resumed DNA synthesis as well as in growing cells never exposed to butyrate. Protein D has been purified from growth-arrested cells and partially sequenced. The amino acid sequences of five internal trypsin peptides indicate that protein D is a novel nuclear protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Autoradiography
  • Butyrates / pharmacology*
  • Butyric Acid
  • Carcinoma, Hepatocellular
  • Cell Cycle / drug effects*
  • Cell Division / drug effects
  • Cell Line
  • DNA Replication / drug effects
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Kinetics
  • Liver Neoplasms
  • Methionine / metabolism
  • Molecular Sequence Data
  • Nuclear Proteins / biosynthesis*
  • Nuclear Proteins / isolation & purification
  • Peptide Fragments / isolation & purification
  • Sulfur Radioisotopes

Substances

  • Butyrates
  • Nuclear Proteins
  • Peptide Fragments
  • Sulfur Radioisotopes
  • Butyric Acid
  • Methionine