首页> 美国卫生研究院文献>Journal of Virology >Selective inhibition of avian sarcoma virus protein synthesis in 3-deazaadenosine-treated infected chicken embryo fibroblasts.
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Selective inhibition of avian sarcoma virus protein synthesis in 3-deazaadenosine-treated infected chicken embryo fibroblasts.

机译:在3-deazaadenosine处理的感染鸡胚成纤维细胞中选择性抑制禽肉瘤病毒蛋白的合成。

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摘要

The production of B77 avian sarcoma virions was inhibited more than 90% in infected chicken embryo fibroblasts that were treated with 100 microM 3-deazaadenosine, an inhibitor of adenosylhomocysteine hydrolase and, for this reason, an inhibitor of methylation reactions. This nucleoside analog at a concentration of 100 microM inhibited the rates of overall cellular protein synthesis and polyadenylated RNA synthesis by 40 to 50%. Rates of viral protein synthesis were compared, and the results indicated that in infected cells treated with 3-deazaadenosine syntheses of both the precursor of the gag proteins (pr76gag) and the precursor of the reverse transcriptase (pr180gag pol) were inhibited. Synthesis of the precursor of the viral envelope glycoproteins (pr92env) appeared to be affected less by the analog treatment. Most of the host polypeptides also continued to be synthesized in 3-deazaadenosine-treated cells. The fraction of the total RNA represented by virus-specific RNA in the 3-deazaadenosine-treated cells was approximately 40% of the fraction of the total RNA represented by viral RNA in control cells, as determined by hybridization kinetics. Therefore, there was a selective inhibition of viral RNA accumulation in the presence of 3-deazaadenosine. The amounts of genome-sized 35S and 38S RNAs were reduced compared with the amounts of 28S and 21S viral mRNA's. These results suggest that selective inhibition of the synthesis of viral proteins is due to selective decreases in the amounts of the mRNA's for these polypeptides.
机译:在用100 microM 3-deazaadenosine处理的感染鸡胚成纤维细胞中,B77禽肉瘤病毒粒子的产生被抑制了90%以上,这是腺苷同型半胱氨酸水解酶的抑制剂,因此是甲基化反应的抑制剂。这种浓度为100 microM的核苷类似物抑制了总体细胞蛋白质合成和聚腺苷酸化RNA合成的速率达40%至50%。比较了病毒蛋白的合成速率,结果表明,在用3-deazaadenosine处理的感染细胞中,gag蛋白前体(pr76gag)和逆转录酶前体(pr180gag pol)的合成均受到抑制。病毒包膜糖蛋白(pr92env)前体的合成似乎受到类似处理的影响较小。大多数宿主多肽还继续在3-deazaadenosine处理的细胞中合成。通过杂交动力学确定,在3-脱氮杂腺苷处理的细胞中,由病毒特异性RNA代表的总RNA的比例约为对照细胞中由病毒RNA代表的总RNA的比例的40%。因此,在3-脱氮杂腺苷的存在下选择性抑制病毒RNA的积累。与28S和21S病毒mRNA的数量相比,基因组大小的35S和38S RNA的数量减少了。这些结果表明,选择性抑制病毒蛋白的合成是由于这些多肽的mRNA的量的选择性降低。

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