1991
DOI: 10.1016/0378-1119(91)90196-i
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The isopycnic, compartmentalized integration of Rous sarcoma virus sequences

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Cited by 46 publications
(23 citation statements)
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References 31 publications
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“…A similar result was obtained with the cellular slime mold, Dyctyostelium discoideum, where five to six copies of the Dirsl transposon were found inserted into the unique region of the same element (Capello, Cohen & Lodish, 1984). In addition, recent investigations carried out in vertebrates (Bernardi, 1989;Rynditch et al, 1991), plants (Capel et al, 1993), and yeast (Moore et al, 1993) have demonstrated that some transposable elements are not randomly distributed in the genomes. Moreover, a group of Drosophila retrotransposons (gypsy, 17.6 and 297) apparently prefer the target sequences TAC/TA and ATAT (Bingham & Zachar, 1979).…”
Section: Introductionsupporting
confidence: 69%
“…A similar result was obtained with the cellular slime mold, Dyctyostelium discoideum, where five to six copies of the Dirsl transposon were found inserted into the unique region of the same element (Capello, Cohen & Lodish, 1984). In addition, recent investigations carried out in vertebrates (Bernardi, 1989;Rynditch et al, 1991), plants (Capel et al, 1993), and yeast (Moore et al, 1993) have demonstrated that some transposable elements are not randomly distributed in the genomes. Moreover, a group of Drosophila retrotransposons (gypsy, 17.6 and 297) apparently prefer the target sequences TAC/TA and ATAT (Bingham & Zachar, 1979).…”
Section: Introductionsupporting
confidence: 69%
“…The concentration of the Tntl family of transposable elements in the GC-poor fractions of the tobacco genome is reminiscent of the compositionally compartmentalized integration of mobile and viral sequences in the genomes of warm-blooded vertebrates (29). …”
Section: Discussionmentioning
confidence: 99%
“…Recently, centromeric alphoid repeats were found to be selectively absent at HIV-1 integration sites (6). A nonrandom, compartmentalized integration in GC-rich isochores has been previously described for human T-cell leukemia virus type 1 (HTLV-1) (52), bovine leukemia virus (22), hepatitis B virus (51), and Rous sarcoma virus (34), while mouse mammary tumor virus has been found to integrate into GC-poor regions (35) of the host genome. At the nucleotide level, in vitro integration reactions and analysis of the flanking sequence of cloned viruses have shown that there is a preference for integration in A/T-rich regions (15,17,27,39).…”
mentioning
confidence: 98%