Granulocytic differentiation of HL-60 cells, both spontaneous and drug-induced, might require loss of extrachromosomal DNA encoding a gene(s) not c-MYC

被引:9
作者
Haque, M [1 ]
Hirano, T [1 ]
Nakamura, H [1 ]
Utiyama, H [1 ]
机构
[1] Hiroshima Univ, Fac Integrated Arts & Sci, Life Sci Grp, Hiroshima 7398521, Japan
关键词
HL-60; c-MYC; differentiation; growth arrest; micronucleus; double minute; gene amplification;
D O I
10.1006/bbrc.2001.5798
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Treatment of HL-60 cells with drugs induces granulocytic differentiation and c-MYC down-regulation that is irreversible and associated with loss of DNase I-hypersensitive sites in c-MYC promoter. The expression of these phenotypes requires a slow process that appears to accompany a loss of c-MYC copies in double minutes via micronuclei. However, the drug treatment induced c-MYC down-regulation very early, though only reversibly. Here we show that we can resolve this paradox by assuming a gene(s) in other extrachromosomal, acentromeric DNA. Treatment with drugs might induce no down-regulation of this gene, but its complete elimination via micronuclei might be necessary and sufficient for the expression of the above phenotypes. Loss of c-MYC copies is unavoidable because the exclusion of extrachromosomal DNAs via micronuclei is at random. This conclusion is based on the observation of a substantial number of c-MYC copies in certain differentiated cells, irrespective of whether the differentiation was induced with drugs or without. (C) 2001 Academic Press.
引用
收藏
页码:586 / 591
页数:6
相关论文
共 33 条
[31]  
TUCKER JD, 1994, CELL BIOL LAB HDB, P450
[32]  
WICKSTROM E, 1992, ANTISENSE RNA DNA, P317
[33]   TRANSCRIPTIONAL CONTROL OF THE ENDOGENOUS MYC PROTOONCOGENE BY ANTISENSE RNA [J].
YOKOYAMA, K ;
IMAMOTO, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7363-7367