1972
DOI: 10.1016/0042-6822(72)90259-0
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Avian reticuloendotheliosis virus (strain T): V. DNA polymerase

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1972
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Cited by 35 publications
(19 citation statements)
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“…In Southern blots with either EcoRI-PstIor HindIll-digested genomic DNA of P.polvcephaluin this fragment hybridized to a 3.5 or 5 kb band, respectively (see Figure 1). Genomic DNA was cut with these restriction enzymes, size selected by sucrose gradient density centrifugation (Peterson et al, 1972) and the corresponding fractions were cloned into pUCl9 and transformed into Ecoli JM83. The size-selected genomic libraries were screened with the 230 bp fragment, and two overlapping genomic clones with sizes of 3.5 and 5 kb were obtained.…”
Section: Methodsmentioning
confidence: 99%
“…In Southern blots with either EcoRI-PstIor HindIll-digested genomic DNA of P.polvcephaluin this fragment hybridized to a 3.5 or 5 kb band, respectively (see Figure 1). Genomic DNA was cut with these restriction enzymes, size selected by sucrose gradient density centrifugation (Peterson et al, 1972) and the corresponding fractions were cloned into pUCl9 and transformed into Ecoli JM83. The size-selected genomic libraries were screened with the 230 bp fragment, and two overlapping genomic clones with sizes of 3.5 and 5 kb were obtained.…”
Section: Methodsmentioning
confidence: 99%
“…However, in contrast to the ALSV group, REVs do not appear to be related to any endogenous type C retrovirus information in avian hosts (21). Moreover, REVs are quite distinct serologically, show little or no nucleic acid homology with members of the ALSV group, and neither genetically complement nor interfere with members of the ALSV group (12,20,22,23,32,38,48). Several studies on the morphology, major structural polypeptides, and DNA polymerase of REVs, presumably focusing on associated helper virus, have suggested that they are more closely related to type C viruses of mammalian origin than to the ALSV group (1,2,18,25,27,51).…”
mentioning
confidence: 98%
“…Preincubation of disrupted virus preparations with RNase significantly decreased the incorporation of [3H]TTP, indicating that the template is RNA, and the product of the polymerase assay was sensitive to DNase but not to RNase. The enzyme thus shares some of the characteristics attributed to polymerases from various other C-type viruses (14)(15)(16). No RDRP activity could be detected in association with the virus.…”
mentioning
confidence: 80%
“…The endogenous polymerase assay was modified from the method of Spiegelman et al (8). A standard incubation mixture of 0.1 ml contained: 0.2 mmole each dATP, dCTP, and dGTP; 0.109 pmole [3H]TTP (15)(16)(17)(18); 2.8 mmole 2-ME; 12 mmole MgCl,; 40 mmole KCl; and 57 mmole Tris-HC1 (pH 8.3). Virus suspended in Tris-HC1 (pH 8.3) was preincubated for 10 min at 0" with 0.08% Nonidet P-40 and 0.4% 2-ME.…”
mentioning
confidence: 99%