首页> 美国卫生研究院文献>Journal of Virology >Isolation identification and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus the etiological agent of sheep pulmonary adenomatosis.
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Isolation identification and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus the etiological agent of sheep pulmonary adenomatosis.

机译:jaagsiekte逆转录病毒(绵羊肺腺瘤病的病原体)的基因组RNA的分离鉴定和部分cDNA克隆。

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摘要

The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. cDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and characterized. It has an insert of 2.1 kb which hybridizes to the same 8.7-kb RNA in all the JSRV-infected sheep lung washes tested but does not hybridize to maedi-visna virus, a sheep lentivirus often found coinfecting JSRV-infected lungs. Comparison of the amino acid sequence encoded by JS 46.1 with those encoded by other retroviruses revealed that JSRV has homology to the type D and B oncoviruses and to human endogenous retrovirus.
机译:绵羊肺腺瘤病(jaagsiekte)的病原体jaagsiekte(JS)逆转录病毒(JSRV)的基因组已被鉴定,分离并部分克隆。 JSRV基因组是约。 8.7 kb长。合成并克隆了基因组RNA的cDNA。分离并鉴定了克隆JS 46.1。它具有2.1 kb的插入片段,可在所有经JSRV感染的绵羊肺洗液中与相同的8.7 kb RNA杂交,但不与maedi-visna病毒(绵羊慢病毒经常与JSRV感染的肺共同感染)杂交。 JS 46.1编码的氨基酸序列与其他逆转录病毒编码的氨基酸序列的比较表明,JSRV与D型和B型癌病毒以及人类内源性逆转录病毒具有同源性。

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