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骨髓增殖性肉瘤病毒基因组分析:原型中的有限变化导致靶细胞特异性改变。

Analysis of the myeloproliferative sarcoma virus genome: limited changes in the prototype lead to altered target cell specificity.

作者信息

Pragnell I B, Fusco A, Arbuthnott C, Smadja-Joffe F, Klein B, Jasmin C, Ostertag W

出版信息

J Virol. 1981 Jun;38(3):952-7. doi: 10.1128/JVI.38.3.952-957.1981.

Abstract

The myeloproliferative sarcoma virus (MPSV) derived from Moloney sarcoma virus (MSV-Mol) is a unique sarcoma virus which causes expansion of the hematopoietic stem cell compartment as well as the erythroid and myeloid cell lineages. MPSV also induces spleen focus formation in adult mice as do Friend and Rauscher viruses. Analysis of the MPSV genome on methyl mercury gels showed that the genome size is 7.0 kilobases, which is larger than the defective genome of any known MSV-Mol isolate. Hybridization analysis with specific cDNA probes showed that MPSV is a modified sarcoma virus with no sequences in the unique region of the defective sarcoma genome related to unique Friend virus sequences. The only viral sequences in the defective genome other than helper virus-related sequences are derived from the Moloney sarcoma virus genome with no new cellular sequences added. There was no evidence for induction of xenotropic virus sequences in MPSV-infected spleens of DBA/2J mice, indicating that spleen focus formation can be obtained by different mechanisms.

摘要

源自莫洛尼肉瘤病毒(MSV-Mol)的骨髓增殖性肉瘤病毒(MPSV)是一种独特的肉瘤病毒,它可导致造血干细胞区室以及红系和髓系细胞谱系的扩增。与弗瑞德病毒和劳舍尔病毒一样,MPSV在成年小鼠中也会诱导脾脏灶形成。在甲基汞凝胶上对MPSV基因组进行分析表明,基因组大小为7.0千碱基,这比任何已知的MSV-Mol分离株的缺陷基因组都要大。用特异性cDNA探针进行的杂交分析表明,MPSV是一种经过修饰的肉瘤病毒,在缺陷肉瘤基因组的独特区域中没有与弗瑞德病毒独特序列相关的序列。除了与辅助病毒相关的序列外,缺陷基因组中唯一的病毒序列源自莫洛尼肉瘤病毒基因组,没有添加新的细胞序列。在感染MPSV的DBA/2J小鼠脾脏中没有诱导嗜异性病毒序列的证据,这表明脾脏灶形成可通过不同机制实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f90/171233/8ddf9cca4b7a/jvirol00006-0158-a.jpg

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