Acceptor sites for retroviral integrations map near DNase I-hypersensitive sites in chromatin

Seven cellular loci with acceptor sites for retroviral integrations have been mapped for the presence of DNase I-hypersensitive sites in chromatin. Integrations in three of these loci, chicken c-erbB, rat c-myc, and a rat locus, dsi-1, had been selected for in retrovirus-induced tumors. Of the remaining four, two, designated dsi-3 and dsi-4, harbored acceptor sites for apparently unselected integrations of Moloney murine leukemia virus in a Moloney murine leukemia virus-induced thymoma, and two, designated C and F, harbored unselected acceptor sites for Moloney murine leukemia virus integrations in a rat fibroblast cell line. Each acceptor site mapped to within 500 base pairs of a DNase I-hypersensitive site. In the analyses of the unselected integrations, six hypersensitive sites were observed in 39 kilobases of DNA. The four acceptor sites in this DNA were localized between 0.05 and 0.43 kilobases of a hypersensitive site. The probability of this close association occurring by chance was calculated to be extremely low. Hypersensitive sites were mapped in cells representing the lineage in which integration had occurred as well as in an unrelated lineage. In six of the seven acceptor loci hypersensitive sites could not be detected in the unrelated lineage. Our results indicate that retroviruses preferentially integrate close to DNase I-hypersensitive sites and that many of these sites are expressed in some but not all cells.

[1]  H. Varmus Form and function of retroviral proviruses. , 1982, Science.

[2]  L. Enquist,et al.  Nucleotide sequences of integrated Moloney sarcoma provirus long terminal repeats and their host and viral junctions. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[3]  M. Groudine,et al.  α-globin-gene switching during the development of chicken embryos: Expression and chromosome structure , 1981, Cell.

[4]  L. Hood,et al.  Introduced T cell receptor variable region gene segments recombine in pre-B cells: Evidence that B and T cells use a common recombinase , 1986, Cell.

[5]  A. E. Sippel,et al.  Alternative sets of DNase I-hypersensitive sites characterize the various functional states of the chicken lysozyme gene , 1984, Nature.

[6]  R. F.,et al.  Mathematical Statistics , 1944, Nature.

[7]  A. Skalka,et al.  Nucleotide sequence analysis of the Long Terminal Repeat (LTR) of avian retroviruses: Structural similarities with transposable elements , 1980, Cell.

[8]  T. Nilsen,et al.  c-erbB activation in ALV-induced erythroblastosis: novel RNA processing and promoter insertion result in expression of an amino-truncated EGF receptor , 1985, Cell.

[9]  H. Robinson,et al.  Patterns of proviral insertion and deletion in avian leukosis virus-induced lymphomas , 1986, Journal of virology.

[10]  J. Bishop,et al.  Isolation and characterization of chicken DNA homologous to the two putative oncogenes of avian erythroblastosis virus , 1982, Cell.

[11]  H. Matthews The structure of transcribing chromatin , 1977, Nature.

[12]  R. Jaenisch,et al.  Retrovirus-induced lethal mutation in collagen I gene of mice is associated with an altered chromatin structure , 1984, Cell.

[13]  Carl Wu The 5′ ends of Drosophila heat shock genes in chromatin are hypersensitive to DNase I , 1980, Nature.

[14]  R. Weinberg,et al.  The integrated genome of murine leukemia virus , 1978, Cell.

[15]  G. Barsh,et al.  DNA and chromatin structure of the human alpha 1 (I) collagen gene. , 1984, The Journal of biological chemistry.

[16]  M. Groudine,et al.  Alteration of c-myc chromatin structure by avian leukosis virus integration , 1984, Nature.

[17]  R. Hawley,et al.  Intracisternal A-particle genes as movable elements in the mouse genome. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[18]  C. Wu,et al.  Tissue-specific exposure of chromatin structure at the 5' terminus of the rat preproinsulin II gene. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[19]  R. Evans,et al.  Expression cloning of human EGF receptor complementary DNA: gene amplification and three related messenger RNA products in A431 cells. , 1984, Science.

[20]  P. Seeburg,et al.  Human epidermal growth factor receptor cDNA sequence and aberrant expression of the amplified gene in A431 epidermoid carcinoma cells , 1984, Nature.

[21]  H. Weintraub Assembly and propagation of repressed and derepressed chromosomal states , 1985, Cell.

[22]  D. Baltimore,et al.  Intramolecular integration within Moloney murine leukemia virus DNA , 1981, Journal of Virology.

[23]  J Gusella,et al.  DNA methylation affecting the expression of murine leukemia proviruses , 1982, Journal of virology.

[24]  H. Robinson,et al.  High-frequency transduction of c-erbB in avian leukosis virus-induced erythroblastosis , 1985, Journal of virology.

[25]  H. Varmus,et al.  Cellular functions are required for the synthesis and integration of avian sarcoma virus-specific DNA , 1977, Cell.

[26]  J. B. Cohen,et al.  Activation of the c-mos oncogene in a mouse plasmacytoma by insertion of an endogenous intracisternal A-particle genome. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[27]  U. Storb,et al.  The switch region associated with immunoglobulin Cμ genes is DNase I hypersensitive in T lymphocytes , 1981, Nature.

[28]  H. Kung,et al.  Activation of the cellular oncogene c-erbB by ltr insertion: Molecular basis for induction of erythroblastosis by avian leukosis virus , 1983, Cell.

[29]  D. Steffen Proviruses are adjacent to c-myc in some murine leukemia virus-induced lymphomas. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[30]  S. Astrin,et al.  Nucleotide sequence of acceptor site and termini of integrated avian endogenous provirus ev1: Integration creates a 6 bp repeat of host DNA , 1981, Cell.

[31]  H. Kung,et al.  c-erbB activation in avian leukosis virus-induced erythroblastosis: clustered integration sites and the arrangement of provirus in the c-erbB alleles. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[32]  A. Ullrich,et al.  Close similarity of epidermal growth factor receptor and v-erb-B oncogene protein sequences , 1984, Nature.

[33]  P. Dehaseth,et al.  Circles with two tandem long terminal repeats are specifically cleaved by pol gene-associated endonuclease from avian sarcoma and leukosis viruses: nucleotide sequences required for site-specific cleavage , 1985, Journal of virology.

[34]  S. Mizutani,et al.  Sequence of retrovirus provirus resembles that of bacterial transposable elements , 1980, Nature.

[35]  T. Graf,et al.  Chicken hematopoietic cells transformed by seven strains of defective avian leukemia viruses display three distinct phenotypes of differentiation , 1979, Cell.

[36]  H. Varmus,et al.  Nucleotide sequences at host–proviral junctions for mouse mammary tumour virus , 1981, Nature.

[37]  P. Philippsen,et al.  Preferential integration of yeast transposable element Ty into a promoter region , 1984, Nature.

[38]  G. Schütz,et al.  Tissue‐specific DNaseI hypersensitive sites in the 5′‐flanking sequences of the tryptophan oxygenase and the tyrosine aminotransferase genes. , 1984, The EMBO journal.

[39]  P. Leder,et al.  Multiple immunoglobulin switch region homologies outside the heavy chain constant region locus , 1981, Nature.