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
[1]  
ARCINAS M, 1994, ONCOGENE, V9, P2699
[2]   DOUBLE MINUTES IN HUMAN-TUMOR CELLS [J].
BARKER, PE .
CANCER GENETICS AND CYTOGENETICS, 1982, 5 (01) :81-94
[3]   A BLOCK TO ELONGATION IS LARGELY RESPONSIBLE FOR DECREASED TRANSCRIPTION OF C-MYC IN DIFFERENTIATED HL60 CELLS [J].
BENTLEY, DL ;
GROUDINE, M .
NATURE, 1986, 321 (6071) :702-706
[4]   A role for serine proteases in mediating phorbol ester-induced differentiation of HL-60 cells [J].
Bestilny, LJ ;
Riabowol, KT .
EXPERIMENTAL CELL RESEARCH, 2000, 256 (01) :264-271
[5]   THE ANTIPROLIFERATIVE ACTIVITY OF C-MYB AND C-MYC ANTISENSE OLIGONUCLEOTIDES IN SMOOTH-MUSCLE CELLS IS CAUSED BY A NONANTISENSE MECHANISM [J].
BURGESS, TL ;
FISHER, EF ;
ROSS, SL ;
BREADY, JV ;
QIAN, YX ;
BAYEWITCH, LA ;
COHEN, AM ;
HERRERA, CJ ;
HU, SSF ;
KRAMER, TB ;
LOTT, FD ;
MARTIN, FH ;
PIERCE, GF ;
SIMONET, L ;
FARRELL, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :4051-4055
[6]   Activation of protein kinase C induces nuclear translocation of RFX1 and down-regulates c-myc via an intron 1 X box in undifferentiated leukemia HL-60 cells [J].
Chen, L ;
Smith, L ;
Johnson, MR ;
Wang, KS ;
Diasio, RB ;
Smith, JB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :32227-32233
[7]   EXTREME INSTABILITY OF MYC MESSENGER-RNA IN NORMAL AND TRANSFORMED HUMAN-CELLS [J].
DANI, C ;
BLANCHARD, JM ;
PIECHACZYK, M ;
ELSABOUTY, S ;
MARTY, L ;
JEANTEUR, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (22) :7046-7050
[8]   CHROMATIN STRUCTURE OF TRANSCRIPTIONALLY ACTIVE AND INACTIVE HUMAN C-MYC ALLELES [J].
DYSON, PJ ;
LITTLEWOOD, TD ;
FORSTER, A ;
RABBITTS, TH .
EMBO JOURNAL, 1985, 4 (11) :2885-2891
[9]   INDUCTION OF DIFFERENTIATION IN HL-60 CELLS BY THE REDUCTION OF EXTRACHROMOSOMALLY AMPLIFIED C-MYC [J].
ECKHARDT, SG ;
DAI, AH ;
DAVIDSON, KK ;
FORSETH, BJ ;
WAHL, GM ;
VONHOFF, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6674-6678
[10]   TRANSCRIPTIONAL ARREST WITHIN THE 1ST EXON IS A FAST CONTROL MECHANISM IN C-MYC GENE-EXPRESSION [J].
EICK, D ;
BORNKAMM, GW .
NUCLEIC ACIDS RESEARCH, 1986, 14 (21) :8331-8346