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. 1989 Jun;63(6):2623–2628. doi: 10.1128/jvi.63.6.2623-2628.1989

Effect of proviral insertion on transcription of the murine B2mb gene.

W N Frankel 1, T A Potter 1, T V Rajan 1
PMCID: PMC250742  PMID: 2542575

Abstract

We describe three B2mb mutants caused by integration of retroviral proviruses into the B2m gene. All three insertions occurred within 500 base pairs of each other in the 5' end of the first intron of the B2mb gene. Mutant cell line i1 contained a nonfunctional Abelson murine leukemia virus-initiated transcript that spliced into B2mb exon II; mutant cell lines i7 and i18 contained transcripts complementary to B2mb exon 1. Both i1 and i7 also contained small amounts of wild-type B2mb transcript. The implications of these studies for the development of retroviral insertional mutagenesis as a strategy for cloning previously uncloned genes are discussed.

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Selected References

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  1. Frankel W., Potter T. A., Rosenberg N., Lenz J., Rajan T. V. Retroviral insertional mutagenesis of a target allele in a heterozygous murine cell line. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6600–6604. doi: 10.1073/pnas.82.19.6600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Geliebter J., Zeff R. A., Melvold R. W., Nathenson S. G. Mitotic recombination in germ cells generated two major histocompatibility complex mutant genes shown to be identical by RNA sequence analysis: Kbm9 and Kbm6. Proc Natl Acad Sci U S A. 1986 May;83(10):3371–3375. doi: 10.1073/pnas.83.10.3371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Geyer P. K., Green M. M., Corces V. G. Reversion of a gypsy-induced mutation at the yellow (y) locus of Drosophila melanogaster is associated with the insertion of a newly defined transposable element. Proc Natl Acad Sci U S A. 1988 Jun;85(11):3938–3942. doi: 10.1073/pnas.85.11.3938. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Goff S. P. Gene isolation by retroviral tagging. Methods Enzymol. 1987;152:469–481. doi: 10.1016/0076-6879(87)52055-9. [DOI] [PubMed] [Google Scholar]
  5. Jaenisch R., Soriano P. Retroviruses as tools for mammalian development. Symp Fundam Cancer Res. 1986;39:59–65. [PubMed] [Google Scholar]
  6. King W., Patel M. D., Lobel L. I., Goff S. P., Nguyen-Huu M. C. Insertion mutagenesis of embryonal carcinoma cells by retroviruses. Science. 1985 May 3;228(4699):554–558. doi: 10.1126/science.3838595. [DOI] [PubMed] [Google Scholar]
  7. Melton D. A., Krieg P. A., Rebagliati M. R., Maniatis T., Zinn K., Green M. R. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 1984 Sep 25;12(18):7035–7056. doi: 10.1093/nar/12.18.7035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mount S. M., Green M. M., Rubin G. M. Partial revertants of the transposable element-associated suppressible allele white-apricot in Drosophila melanogaster: structures and responsiveness to genetic modifiers. Genetics. 1988 Feb;118(2):221–234. doi: 10.1093/genetics/118.2.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Nelson F. K., Frankel W., Rajan T. V. Mitotic recombination is responsible for the loss of heterozygosity in cultured murine cell lines. Mol Cell Biol. 1989 Mar;9(3):1284–1288. doi: 10.1128/mcb.9.3.1284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Nilsen T. W., Maroney P. A., Goodwin R. G., Rottman F. M., Crittenden L. B., Raines M. A., Kung H. J. c-erbB activation in ALV-induced erythroblastosis: novel RNA processing and promoter insertion result in expression of an amino-truncated EGF receptor. Cell. 1985 Jul;41(3):719–726. doi: 10.1016/s0092-8674(85)80052-0. [DOI] [PubMed] [Google Scholar]
  11. Parnes J. R., Sizer K. C., Seidman J. G., Stallings V., Hyman R. A mutational hot-spot within an intron of the mouse beta 2-microglobulin gene. EMBO J. 1986 Jan;5(1):103–111. doi: 10.1002/j.1460-2075.1986.tb04183.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Potter T. A., Frankel W., Zeff R. A., Rajan T. V. Spontaneous deletion at the B2m locus: evidence for site-specific genetic rearrangement. J Immunol. 1987 Feb 15;138(4):1270–1274. [PubMed] [Google Scholar]
  13. Reddy E. P., Smith M. J., Srinivasan A. Nucleotide sequence of Abelson murine leukemia virus genome: structural similarity of its transforming gene product to other onc gene products with tyrosine-specific kinase activity. Proc Natl Acad Sci U S A. 1983 Jun;80(12):3623–3627. doi: 10.1073/pnas.80.12.3623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Shen-Ong G. L., Morse H. C., 3rd, Potter M., Mushinski J. F. Two modes of c-myb activation in virus-induced mouse myeloid tumors. Mol Cell Biol. 1986 Feb;6(2):380–392. doi: 10.1128/mcb.6.2.380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Siracusa L. D., Russell L. B., Eicher E. M., Corrow D. J., Copeland N. G., Jenkins N. A. Genetic organization of the agouti region of the mouse. Genetics. 1987 Sep;117(1):93–100. doi: 10.1093/genetics/117.1.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Varmus H. E., Quintrell N., Ortiz S. Retroviruses as mutagens: insertion and excision of a nontransforming provirus alter expression of a resident transforming provirus. Cell. 1981 Jul;25(1):23–36. doi: 10.1016/0092-8674(81)90228-2. [DOI] [PubMed] [Google Scholar]

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