Shank P R, Schatz P J, Jensen L M, Tsichlis P N, Coffin J M, Robinson H L
Virology. 1985 Aug;145(1):94-104. doi: 10.1016/0042-6822(85)90204-1.
DNA sequences encoding the genomes of three subgroup E avian leukosis viruses have been molecularly cloned. Virus recovered from one of these cloned DNAs (pRAV-0) caused no osteopetrosis while virus recovered from the second (lambda NY203) caused late onset osteopetrosis and virus recovered from the third (lambda NTRE-2) caused intermediate onset osteopetrosis. Restriction endonuclease fragments of the cloned viral DNAs were used to construct recombinant viruses that could be used to test for the role of gag-pol-5'env and 3'env-LTR sequences in the induction of osteopetrosis. The results of the pathogenicity tests indicate that gag-pol-5'env sequences confer the ability to induce osteopetrosis while 3'env-LTR sequences influence the time of onset and the severity of osteopetrosis.
编码三种E亚群禽白血病病毒基因组的DNA序列已被分子克隆。从其中一个克隆DNA(pRAV-0)中回收的病毒不会引起骨质石化,而从第二个克隆DNA(λNY203)中回收的病毒会引起迟发性骨质石化,从第三个克隆DNA(λNTRE-2)中回收的病毒会引起中度骨质石化。克隆病毒DNA的限制性内切酶片段被用于构建重组病毒,这些重组病毒可用于测试gag-pol-5'env和3'env-LTR序列在骨质石化诱导中的作用。致病性测试结果表明,gag-pol-5'env序列赋予了诱导骨质石化的能力,而3'env-LTR序列影响骨质石化的发病时间和严重程度。