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鉴定用于合成gag和env基因产物的劳氏肉瘤小鼠白血病病毒特异性mRNA。

Identification of Rauscher murine leukemia virus-specific mRNAs for the synthesis of gag- and env-gene products.

作者信息

Zaane D V, Gielkens A L, Hesselink W G, Bloemers H P

出版信息

Proc Natl Acad Sci U S A. 1977 May;74(5):1855-9. doi: 10.1073/pnas.74.5.1855.

Abstract

Polyadenylylated mRNA isolated from cells infected with Rauscher murine leukemia virus was fractionated by centrifugation in in a denaturing sucrose gradient into different sizes. Each RNA fraction was injected into oocytes of Xenopus laevis and the virus-specific products were analyzed by immunoprecipitation with polyvalent and monospecific antisera against polypeptides of Rauscher murine leukemia virus, and then by gel electrophoresis and scintillation autoradiography. It was shown that a 35S mRNA species directs the synthesis of a precursor of the internal or group-specific antigens of the virion (the gag-gene products). A 22S mRNA species directs the synthesis of two viral envelope polypeptides and their precursor polypeptide (env-gene products). The results indicate that the gag- and env-related polypeptides of Rauscher murine leukemia virus are synthesized uncoordinately and provide evidence for open and closed cistrons on the virus-specific mRNAs.

摘要

从感染劳斯氏鼠白血病病毒的细胞中分离出的多聚腺苷酸化mRNA,通过在变性蔗糖梯度中离心,按大小进行分级分离。将每个RNA级分注射到非洲爪蟾的卵母细胞中,并用针对劳斯氏鼠白血病病毒多肽的多价和单特异性抗血清通过免疫沉淀分析病毒特异性产物,然后通过凝胶电泳和闪烁放射自显影进行分析。结果表明,一种35S mRNA种类指导病毒粒子内部或群特异性抗原前体(gag基因产物)的合成。一种22S mRNA种类指导两种病毒包膜多肽及其前体多肽(env基因产物)的合成。结果表明,劳斯氏鼠白血病病毒的gag和env相关多肽是不协调合成的,并为病毒特异性mRNA上的开放和闭合顺反子提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bf/431029/a70ab9197862/pnas00027-0099-a.jpg

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