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.