首页> 外文期刊>Journal of Virology >Influenza virus-specific RNA and protein syntheses in cells infected with temperature-sensitive mutants defective in the genome segment encoding nonstructural proteins.
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Influenza virus-specific RNA and protein syntheses in cells infected with temperature-sensitive mutants defective in the genome segment encoding nonstructural proteins.

机译:流感病毒特异性RNA和蛋白质在感染的细胞中,在编码非结构蛋白的基​​因组区段中缺陷缺陷。

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Virus-specific protein and RNA syntheses have been analyzed in chicken embryo fibroblast cells infected with two group IV temperature-sensitive (ts) mutants of influenza A (fowl plague) virus in which the ts lesion maps in RNA segment 8 (J. W. Almond, D. McGeoch, and R. D. Barry, Virology 92:416-427, 1979), known to code to code for two nonstructural proteins, NS1 and NS2. Both mutants induced the synthesis of similar amounts of all the early virus-specific proteins (P1, P2, P3, NP, and NS1) at temperatures that were either permissive (34 degrees C) or nonpermissive (40.5 degrees C) for replication. However, the synthesis of M protein, which normally accumulates late in infection, was greatly reduced in ts mutant-infected cells at 40.5 degrees C compared to 34 degrees C. The NS2 protein was not detected at either temperature in cells infected with one mutant (mN3), and was detected only at the permissive temperature in cells infected with mutant ts47. There was no overall reduction in polyadenylated (A+) complementary RNA, which functions as mRNA, in cells infected with these mutants at 40.5 degrees C compared to 34 degrees C, nor was there any evidence of selective accumulation of this type of RNA within the nucleus at the nonpermissive temperature. No significant differences in ts mutant virion RNA transcriptase activity were detected by assays in vitro at 31 and 40.5 degrees C compared to wild-type virus. Virus-specific non-polyadenylated (A-) complementary RNA, which is believed to act as the template for new virion RNA production, accumulated normally in cells at both 34 and 40.5 degrees C, but at 40.5 degrees C accumulation of new virion RNA was reduced by greater than 90% when compared to accumulation at 34 degrees C.
机译:已经在感染的鸡胚胚胎成纤维细胞中分析了特异性蛋白质和RNA合成,其中血型血型血型血型血型族β(FOWL瘟疫)病毒的两组温度敏感(TS)突变体,其中TS病变在RNA段8(JW Almond,D. 。McGeoch,RD Barry,Virology 92:416-427,1979)已知两个非结构蛋白,NS1和NS2的代码。两个突变体在允许(34℃)或非智能(40.5℃)的温度下,诱导了所有早期病毒特异性蛋白质(P1,P2,P3,NP和NP和NS1)的合成。然而,与34℃相比,在40.5℃下,在TS突变感染细胞中大大减少了通常积累的M蛋白的合成。在感染一个突变体的细胞中未检测到NS2蛋白在任何一个温度下未检测到NS2蛋白(仅在用突变体TS47感染的细胞中的允许温度下检测MN3)。在40.5℃下,在用40.5℃的细胞中,在感染这些突变体的细胞中,不存在作为mRNA的多腺苷酸化(A +)互补RNA的总体减少,与34℃,也没有任何证据表明这种类型的RNA在核中的选择性积累的证据在非智能温度下。与野生型病毒相比,通过在31和40.5℃的体外测定,检测到TS突变病毒赛RNA转录酶活性的显着差异。特异性的非聚腺苷酸化(A-)互补RNA,其被认为是新的病毒杆菌RNA生产的模板,通常在34和40.5℃的细胞中累积,但在40.5摄氏度的新病毒虫RNA的积累中与34摄氏度的积累相比,减少大于90%。

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