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一种新的禽成红细胞增多症病毒,AEV-H,携带erbB基因,该基因可导致成红细胞增多症和肉瘤。

A new avian erythroblastosis virus, AEV-H, carries erbB gene responsible for the induction of both erythroblastosis and sarcomas.

作者信息

Yamamoto T, Hihara H, Nishida T, Kawai S, Toyoshima K

出版信息

Cell. 1983 Aug;34(1):225-32. doi: 10.1016/0092-8674(83)90153-8.

Abstract

The genome structure of a newly isolated avian erythroblastosis virus, AEV-H, was analyzed. Using DNA probes specific for the LTR sequence of SR-RSV-A, and for the erbA gene and the erbB gene of the ES4 strain of AEV, we have shown that the genome of AEV-H is 35S in size and carries the erbB gene but not the erbA gene. Comparison of the restriction sites of molecularly cloned AEV-H DNA with that of cloned DNA of the associated virus revealed that the env gene of the associated virus was replaced with the erbB gene to generate AEV-H. The genome structure of AEV-H is, therefore, determined to be 5'-gag-pol-erbB-3'. Moreover, we have isolated a mutant of AEV-H, td-130, that can induce sarcomas but not erythroblastosis in chickens. The restriction analysis of proviral DNA of the td-130 showed that it carries a deletion of about 150 to 200 nucleotides in the erbB gene. These data indicate that the erbB protein is responsible for both erythroblastosis and sarcomas.

摘要

对新分离出的禽成红细胞增多症病毒AEV-H的基因组结构进行了分析。使用针对SR-RSV-A的LTR序列以及AEV的ES4株的erbA基因和erbB基因的DNA探针,我们已表明AEV-H的基因组大小为35S,携带erbB基因但不携带erbA基因。将分子克隆的AEV-H DNA的限制性酶切位点与相关病毒的克隆DNA的限制性酶切位点进行比较,发现相关病毒的env基因被erbB基因取代从而产生了AEV-H。因此,AEV-H的基因组结构被确定为5'-gag-pol-erbB-3'。此外,我们分离出了AEV-H的一个突变体td-130,它能在鸡中诱导肉瘤但不能诱导成红细胞增多症。对td-130的前病毒DNA的限制性分析表明,它在erbB基因中存在约150至200个核苷酸的缺失。这些数据表明erbB蛋白对成红细胞增多症和肉瘤都起作用。

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