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首页> 外文期刊>Journal of Virology >Characterization of avian myeloblastosis-associated virus DNA intermediates.
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Characterization of avian myeloblastosis-associated virus DNA intermediates.

机译:禽髓母细胞栓塞相关病毒DNA中间体的特征。

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The major species of unintegrated linear viral DNA identified in chicken embryonic fibroblasts infected with either the avian myeloblastosis-associated viruses (MAV-1, MAV-2) or the standard avian myeloblastosis virus complex (AMV-S) has a mass of 5.3 X 10(6) daltons. An additional minor DNA component observed only in AMV-S-infected cells has a mass of 4.9 X 10(6) daltons. The unintegrated linear viral DNAs and integrated proviruses of MAV-1 and MAV-2 have been analyzed by digestion with the restriction endonucleases EcoRI and HindIII. MAV-2 lacks a HindIII site present in MAV-1. These fragments have been compared to those generated by EcoRI and HindIII digestion of linear viral DNAs of AMV-S. Restriction enzyme digestion of AMV-S viral DNA produced unique fragments not found with either MAV-1 or MAV-2 viral DNAs. The major viral component present in AMV-S stocks has the HindIII restriction pattern of MAV-1. Restriction enzyme analysis of the 5.3 X 10(6)-dalton unintegrated MAV viral DNAs and their integrated proviruses suggests that the DNAs have a direct terminal redundancy of approximately 0.3 megadaltons and integrate colinearly with respect to the unintegrated linear DNA.
机译:鸡胚胎成纤维细胞中鉴定的未经聚糖线性病毒DNA的主要种类,感染禽髓霉菌栓塞相关病毒(MAV-1,MAV-2)或标准禽髓母细胞化病毒复合物(AMV-S)的质量为5.3×10 (6)道尔顿。仅在AMV-S感染的细胞中观察到的另外的次要DNA组分具有4.9×10(6)道尔顿的质量。通过用限制性内切核酸酶生态和HindIII消化,通过消化分析了未成期的线性病毒DNA和MAV-1和MAV-2的综合潜水。 MAV-2缺乏MAV-1中存在的HINDIII网站。已经将这些片段与EcoRI和HindiII消化的amv-s的线性病毒DNA产生的那些进行了比较。 IMV-S病毒DNA的限制酶消化产生了用MAV-1或MAV-2病毒DNA未发现的独特片段。 AMV-S股中存在的主要病毒组分具有MAV-1的HINDIII限制模式。 5.3×10(6)-Dalton未成化的MAV病毒DNA及其集成潜艇的限制酶分析表明DNA具有约0.3megadaltons的直接末端冗余,并相对于未受整治线性DNA集成。

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