Literature DB >> 9336478

A rapid RT-PCR based method to isolate complementary DNA fragments flanking retrovirus integration sites.

P J Valk1, M Joosten, Y Vankan, B Löwenberg, R Delwel.   

Abstract

Proto-oncogenes in retrovirally induced myeloid mouse leukemias are frequently activated following retroviral insertion. The identification of common virus integration sites (VISs) and isolation of the transforming oncogene is laborious and time consuming. We established a rapid and simple PCR based procedure which facilitates the identification of VISs and novel proto-oncogenes. Complementary DNA fragments adjacent to retrovirus integration sites were selectively isolated by applying a reverse transcriptase (RT) reaction using an oligo(dT)-adaptor primer, followed by PCR using the adaptor sequence and a retrovirus long terminal repeat (LTR) specific primer. Multiple chimeric cDNA fragments suitable for Southern and northern blot analysis were isolated.

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Year:  1997        PMID: 9336478      PMCID: PMC147027          DOI: 10.1093/nar/25.21.4419

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  18 in total

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Authors:  J Silver; V Keerikatte
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5.  His-1 and His-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.

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Journal:  Nucleic Acids Res       Date:  1996-03-01       Impact factor: 16.971

7.  Promoter region of mouse Tcrg genes.

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Authors:  C Bartholomew; K Morishita; D Askew; A Buchberg; N A Jenkins; N G Copeland; J N Ihle
Journal:  Oncogene       Date:  1989-05       Impact factor: 9.867

10.  Correlation of cell-surface phenotype with the establishment of interleukin 3-dependent cell lines from wild-mouse murine leukemia virus-induced neoplasms.

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4.  K1 protein of human herpesvirus 8 suppresses lymphoma cell Fas-mediated apoptosis.

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  5 in total

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