Exp Mol Med.  1998 Dec;30(4):252-256.

Down-regulation of human FEN-1 gene expression during differentiation of promyelocytic leukemia cells

Affiliations
  • 1Department of Natural Sciences Chemistry Section, Catholic University of Korea College of Medicine, Seoul, Korea. ikim@cmc.cuk.ac.kr

Abstract

Flap endo/exonuclease-1 (FEN-1) recognizes 5'-flap DNA structures that have been proposed to be important intermediates in DNA replication, repair and recombination, and cleaves the double strand-single strand junction of flap substrates. Using an in vitro model system, recent studies have shown that FEN-1 is a necessary enzyme for the removal of RNA primers in Okazaki fragment maturation during lagging strand DNA synthesis. In this report, the FEN-1 gene expression was examined during cell cycle and differentiation. Although FEN-1 mRNA and protein could be detected at all stages of the cell cycle, their levels were more elevated in exponentially proliferating cells than in G1 or G2/M-synchronized cells. Moreover, a significant increase of FEN-1 protein was observed when temporarily quiescent fibroblasts were induced to proliferate by serum stimulation. In contrast, the FEN-1 mRNA level showed a sharp decrease in HL-60 cells differentiated by dimethyl-sulfoxide, all-trans retinoic acid or 12-O-tetradecanoylphorbol-13-acetate. These results demonstrate that the FEN-1 gene expression is up-regulated during entrance into the mitotic cell cycle and down-regulated in nongrowing cells, as in the case of differentiated promyelocytic leukemia cells.

Keyword

Cell differentiation; FEN-1; Gene expression; HL-60 cells

MeSH Terms

3T3 Cells
Animal
Blotting, Western
Cell Cycle/genetics
Cell Differentiation
Cell Division/genetics*
Dimethyl Sulfoxide/pharmacology
Down-Regulation (Physiology)
Endodeoxyribonucleases/genetics*
Flow Cytometry
Gene Expression Regulation, Neoplastic*
HL-60 Cells
Human
Leukemia, Promyelocytic, Acute/genetics*
Mice
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