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. 1989 Oct;86(19):7442–7445. doi: 10.1073/pnas.86.19.7442

Loss of the MYC gene amplified in human HL-60 cells after treatment with inhibitors of poly(ADP-ribose) polymerase or with dimethyl sulfoxide.

H Shima 1, M Nakayasu 1, S Aonuma 1, T Sugimura 1, M Nagao 1
PMCID: PMC298080  PMID: 2529540

Abstract

In HL-60 cells, a human promyelocytic leukemia cell line, the human c-myc gene, designated MYC, is amplified about 16-fold. On differentiation of the HL-60 cells into granulocytes induced by several inhibitors of poly(ADP-ribose) polymerase [NAD+ poly(adenosine diphosphate D-ribose)ADP-D-ribosyltransferase, EC 2.4.2.30] including benzamide, nicotinamide, coumarin, and 4-hydroxyquinazoline or dimethyl sulfoxide, some MYC loss was observed. In contrast, benzoic acid, a noninhibitory analogue of benzamide, did not induce either granulocytic differentiation or loss of MYC. Loss of MYC seems to be associated with granulocytic differentiation because the time course of its loss was similar to that of appearance of nitroblue tetrazolium-positive cells, mature granulocytes, and its loss was not observed on differentiation of HL-60 cells into macrophages induced by phorbol 12-myristate 13-acetate or teleocidin. The loss of MYC is not the reason for the down regulation of MYC expression observed within 1 hr after addition of inducers, since the loss of MYC was not detected by 1-day treatment with inducers.

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Selected References

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  1. Alitalo K., Schwab M., Lin C. C., Varmus H. E., Bishop J. M. Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma. Proc Natl Acad Sci U S A. 1983 Mar;80(6):1707–1711. doi: 10.1073/pnas.80.6.1707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bentley D. L., Groudine M. A block to elongation is largely responsible for decreased transcription of c-myc in differentiated HL60 cells. Nature. 1986 Jun 12;321(6071):702–706. doi: 10.1038/321702a0. [DOI] [PubMed] [Google Scholar]
  3. Carroll S. M., DeRose M. L., Gaudray P., Moore C. M., Needham-Vandevanter D. R., Von Hoff D. D., Wahl G. M. Double minute chromosomes can be produced from precursors derived from a chromosomal deletion. Mol Cell Biol. 1988 Apr;8(4):1525–1533. doi: 10.1128/mcb.8.4.1525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  5. Collins S. J. The HL-60 promyelocytic leukemia cell line: proliferation, differentiation, and cellular oncogene expression. Blood. 1987 Nov;70(5):1233–1244. [PubMed] [Google Scholar]
  6. Eick D., Bornkamm G. W. Transcriptional arrest within the first exon is a fast control mechanism in c-myc gene expression. Nucleic Acids Res. 1986 Nov 11;14(21):8331–8346. doi: 10.1093/nar/14.21.8331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gezer S., Yasin Z., Imren S., Freeman J., Black A., Raza A. Changes observed in the growth fraction, labeling index, duration of S phase, and total cell cycle times of HL-60 cells as they undergo differentiation in response to retinoic acid. Cancer Res. 1988 Nov 1;48(21):5989–5994. [PubMed] [Google Scholar]
  8. Grosso L. E., Pitot H. C. Modulation of c-myc expression in the HL-60 cell line. Biochem Biophys Res Commun. 1984 Mar 15;119(2):473–480. doi: 10.1016/s0006-291x(84)80273-9. [DOI] [PubMed] [Google Scholar]
  9. Hamlin J. L., Milbrandt J. D., Heintz N. H., Azizkhan J. C. DNA sequence amplification in mammalian cells. Int Rev Cytol. 1984;90:31–82. doi: 10.1016/s0074-7696(08)61487-4. [DOI] [PubMed] [Google Scholar]
  10. High K. A., Stolle C. A., Schneider J. W., Hu W., Benz E. J., Jr c-myc gene inactivation during induced maturation of HL-60 cells. Transcriptional repression and loss of a specific DNAse I hypersensitive site. J Clin Invest. 1987 Jan;79(1):93–99. doi: 10.1172/JCI112814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kameshita I., Matsuda Z., Taniguchi T., Shizuta Y. Poly (ADP-Ribose) synthetase. Separation and identification of three proteolytic fragments as the substrate-binding domain, the DNA-binding domain, and the automodification domain. J Biol Chem. 1984 Apr 25;259(8):4770–4776. [PubMed] [Google Scholar]
  12. Kanai M., Miwa M., Kondo T., Tanaka Y., Nakayasu M., Sugimura T. Involvement of poly (ADP-ribose) metabolism in induction of differentiation of HL-60 promyelocytic leukemia cells. Biochem Biophys Res Commun. 1982 Mar 30;105(2):404–411. doi: 10.1016/0006-291x(82)91448-6. [DOI] [PubMed] [Google Scholar]
  13. Lönn U., Lönn S. Accumulation of 10-kilobase DNA replication intermediates in cells treated with 3-aminobenzamide. Proc Natl Acad Sci U S A. 1985 Jan;82(1):104–108. doi: 10.1073/pnas.82.1.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Maurer B. J., Lai E., Hamkalo B. A., Hood L., Attardi G. Novel submicroscopic extrachromosomal elements containing amplified genes in human cells. Nature. 1987 Jun 4;327(6121):434–437. doi: 10.1038/327434a0. [DOI] [PubMed] [Google Scholar]
  15. Misawa S., Staal S. P., Testa J. R. Amplification of the c-myc oncogene is associated with an abnormally banded region on chromosome 8 or double minute chromosomes in two HL-60 human leukemia sublines. Cancer Genet Cytogenet. 1987 Sep;28(1):127–135. doi: 10.1016/0165-4608(87)90362-1. [DOI] [PubMed] [Google Scholar]
  16. Nakayasu M., Shima H., Aonuma S., Nakagama H., Nagao M., Sugimura T. Deletion of transfected oncogenes from NIH 3T3 transformants by inhibitors of poly(ADP-ribose) polymerase. Proc Natl Acad Sci U S A. 1988 Dec;85(23):9066–9070. doi: 10.1073/pnas.85.23.9066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Nowell P., Finan J., Dalla-Favera R., Gallo R. C., ar-Rushdi A., Romanczuk H., Selden J. R., Emanuel B. S., Rovera G., Croce C. M. Association of amplified oncogene c-myc with an abnormally banded chromosome 8 in a human leukaemia cell line. Nature. 1983 Dec 1;306(5942):494–497. doi: 10.1038/306494a0. [DOI] [PubMed] [Google Scholar]
  18. Nudel U., Zakut R., Shani M., Neuman S., Levy Z., Yaffe D. The nucleotide sequence of the rat cytoplasmic beta-actin gene. Nucleic Acids Res. 1983 Mar 25;11(6):1759–1771. doi: 10.1093/nar/11.6.1759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Oikawa A., Tohda H., Kanai M., Miwa M., Sugimura T. Inhibitors of poly(adenosine diphosphate ribose) polymerase induce sister chromatid exchanges. Biochem Biophys Res Commun. 1980 Dec 31;97(4):1311–1316. doi: 10.1016/s0006-291x(80)80009-x. [DOI] [PubMed] [Google Scholar]
  20. Oka J., Ueda K., Hayaishi O., Komura H., Nakanishi K. ADP-ribosyl protein lyase. Purification, properties, and identification of the product. J Biol Chem. 1984 Jan 25;259(2):986–995. [PubMed] [Google Scholar]
  21. Ruiz J. C., Choi K. H., von Hoff D. D., Roninson I. B., Wahl G. M. Autonomously replicating episomes contain mdr1 genes in a multidrug-resistant human cell line. Mol Cell Biol. 1989 Jan;9(1):109–115. doi: 10.1128/mcb.9.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schimke R. T. Gene amplification in cultured animal cells. Cell. 1984 Jul;37(3):705–713. doi: 10.1016/0092-8674(84)90406-9. [DOI] [PubMed] [Google Scholar]
  23. Schwartz D. C., Cantor C. R. Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis. Cell. 1984 May;37(1):67–75. doi: 10.1016/0092-8674(84)90301-5. [DOI] [PubMed] [Google Scholar]
  24. Siebenlist U., Bressler P., Kelly K. Two distinct mechanisms of transcriptional control operate on c-myc during differentiation of HL60 cells. Mol Cell Biol. 1988 Feb;8(2):867–874. doi: 10.1128/mcb.8.2.867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Stark G. R., Wahl G. M. Gene amplification. Annu Rev Biochem. 1984;53:447–491. doi: 10.1146/annurev.bi.53.070184.002311. [DOI] [PubMed] [Google Scholar]
  26. Sugimura T. Poly(adenosine diphosphate ribose). Prog Nucleic Acid Res Mol Biol. 1973;13:127–151. doi: 10.1016/s0079-6603(08)60102-6. [DOI] [PubMed] [Google Scholar]
  27. Suzuki H., Uchida K., Shima H., Sato T., Okamoto T., Kimura T., Miwa M. Molecular cloning of cDNA for human poly(ADP-ribose) polymerase and expression of its gene during HL-60 cell differentiation. Biochem Biophys Res Commun. 1987 Jul 31;146(2):403–409. doi: 10.1016/0006-291x(87)90543-2. [DOI] [PubMed] [Google Scholar]
  28. Tseng A., Jr, Lee W. M., Jakobovits E. B., Kirsten E., Hakam A., McLick J., Buki K., Kun E. Prevention of tumorigenesis of oncogene-transformed rat fibroblasts with DNA site inhibitors of poly(ADP ribose) polymerase. Proc Natl Acad Sci U S A. 1987 Feb;84(4):1107–1111. doi: 10.1073/pnas.84.4.1107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Von Hoff D. D., Needham-VanDevanter D. R., Yucel J., Windle B. E., Wahl G. M. Amplified human MYC oncogenes localized to replicating submicroscopic circular DNA molecules. Proc Natl Acad Sci U S A. 1988 Jul;85(13):4804–4808. doi: 10.1073/pnas.85.13.4804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Watson R., Oskarsson M., Vande Woude G. F. Human DNA sequence homologous to the transforming gene (mos) of Moloney murine sarcoma virus. Proc Natl Acad Sci U S A. 1982 Jul;79(13):4078–4082. doi: 10.1073/pnas.79.13.4078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Westin E. H., Wong-Staal F., Gelmann E. P., Dalla-Favera R., Papas T. S., Lautenberger J. A., Eva A., Reddy E. P., Tronick S. R., Aaronson S. A. Expression of cellular homologues of retroviral onc genes in human hematopoietic cells. Proc Natl Acad Sci U S A. 1982 Apr;79(8):2490–2494. doi: 10.1073/pnas.79.8.2490. [DOI] [PMC free article] [PubMed] [Google Scholar]

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