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1
Measles virus ribonucleic acid and protein synthesis: effects of 6-azauridine and cycloheximide on viral replication.麻疹病毒核糖核酸与蛋白质合成:6-氮尿苷和环己酰亚胺对病毒复制的影响
J Virol. 1973 Jan;11(1):46-53. doi: 10.1128/JVI.11.1.46-53.1973.
2
Induction of measles virus hemagglutinin in a persistently infected, nonvirogenic line of cells (BGM/MV).在持续感染的非产病毒细胞系(BGM/MV)中诱导麻疹病毒血凝素
J Virol. 1976 Mar;17(3):1052-5. doi: 10.1128/JVI.17.3.1052-1055.1976.
3
Latency of human measles virus in hamster cells.人麻疹病毒在仓鼠细胞中的潜伏期。
J Virol. 1972 Nov;10(5):995-1001. doi: 10.1128/JVI.10.5.995-1001.1972.
4
Replication of measles virus: continued synthesis of nucleocapsid RNA and increased synthesis of mRNA in the presence of cycloheximide.麻疹病毒的复制:在放线菌酮存在的情况下持续合成核衣壳RNA并增加mRNA的合成。
J Virol. 1974 Oct;14(4):758-64. doi: 10.1128/JVI.14.4.758-764.1974.
5
The effect of cycloheximide on the replication of measles virus.放线菌酮对麻疹病毒复制的影响。
J Gen Virol. 1977 Jun;35(3):579-82. doi: 10.1099/0022-1317-35-3-579.
6
The effect of a carbobenzoxy tripeptide on the biological activities of measles virus.苄氧羰基三肽对麻疹病毒生物学活性的影响。
Virology. 1971 Jun;44(3):599-608. doi: 10.1016/0042-6822(71)90374-6.
7
Studies on the assembly of Newcastle disease virus: an arginine-dependent step in virus replication.新城疫病毒装配的研究:病毒复制中一个依赖精氨酸的步骤。
Virology. 1973 Jan;51(1):205-15. doi: 10.1016/0042-6822(73)90380-2.
8
A salt-dependent hemagglutinating particle from measles-infected cells.一种来自麻疹感染细胞的依赖盐的血凝颗粒。
Virology. 1967 Oct;33(2):297-306. doi: 10.1016/0042-6822(67)90148-1.
9
Mechanisms of vesicular stomatitis virus-induced cytopathic effects. I. Early morphologic changes induced by infectious and defective-interfering particles.水泡性口炎病毒诱导细胞病变效应的机制。I. 感染性颗粒和缺陷干扰颗粒诱导的早期形态学变化。
Virology. 1976 Jul 15;72(2):370-82. doi: 10.1016/0042-6822(76)90166-5.
10
Studies on peristent infection of WISH cell line with measles virus.关于麻疹病毒对WISH细胞系持续感染的研究。
Acta Microbiol Pol A. 1973;5(3):241-3.

引用本文的文献

1
Host DNA synthesis-suppressing factor in culture fluid of tissue cultures infected with measles virus.麻疹病毒感染的组织培养物培养液中的宿主DNA合成抑制因子。
J Virol. 1974 May;13(5):1118-25. doi: 10.1128/JVI.13.5.1118-1125.1974.
2
Analysis of bovine parainfluenza-3 virus replication in bovine embryonic lung cells by indirect fluorescent antibody and hemadsorption assays.通过间接荧光抗体和血细胞吸附试验分析牛副流感3型病毒在牛胚胎肺细胞中的复制情况。
J Virol Methods. 1990 Jan;27(1):113-9. doi: 10.1016/0166-0934(90)90151-5.
3
Paramyxovirus-avian cell relationship: discrepant impact of 6-azauridine on virus production by susceptible and less susceptible cells.副粘病毒与禽类细胞的关系:6-氮杂尿苷对易感细胞和较不易感细胞产生病毒的不同影响。
Infect Immun. 1975 May;11(5):915-8. doi: 10.1128/iai.11.5.915-918.1975.
4
Activation of measles virus from silently infected human lymphocytes.从潜伏感染的人类淋巴细胞中激活麻疹病毒。
J Exp Med. 1978 Oct 1;148(4):940-52. doi: 10.1084/jem.148.4.940.
5
Measles virus and its associated diseases.麻疹病毒及其相关疾病。
Bacteriol Rev. 1977 Sep;41(3):636-66. doi: 10.1128/br.41.3.636-666.1977.
6
In vitro studies on Borna virus. II. Properties of the virus.
Arch Virol. 1979;61(4):261-71. doi: 10.1007/BF01315012.

本文引用的文献

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MEASLES VIRUS.麻疹病毒
Arch Gesamte Virusforsch. 1965;16:57-80. doi: 10.1007/BF01253793.
2
DELAY IN THE MULTIPLICATION OF INFLUENZA VIRUS.流感病毒增殖的延迟
Virology. 1965 Feb;25:289-302. doi: 10.1016/0042-6822(65)90207-2.
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INHIBITION OF RIBONUCLEIC ACID SYNTHESIS IN NEWCASTLE DISEASE VIRUS-INFECTED CELLS BY PUROMYCIN AND 6-AZAURIDINE.嘌呤霉素和6-氮杂尿苷对新城疫病毒感染细胞中核糖核酸合成的抑制作用
J Bacteriol. 1964 Dec;88(6):1550-5. doi: 10.1128/jb.88.6.1550-1555.1964.
4
CYCLOHEXIMIDE: ASPECTS OF INHIBITION OF PROTEIN SYNTHESIS IN MAMMALIAN CELLS.环己酰亚胺:哺乳动物细胞中蛋白质合成抑制的相关方面
Science. 1964 Dec 11;146(3650):1474-6. doi: 10.1126/science.146.3650.1474.
5
Use of actinomycin D to unmask RNA synthesis induced by Newcastle disease virus.
Biochem Biophys Res Commun. 1962 Sep 25;9:156-61. doi: 10.1016/0006-291x(62)90106-7.
6
Conparative studies of RNA and protein synthesis with a myxovirus and a small polyhedral virus.关于一种黏液病毒和一种小型多面体病毒的RNA和蛋白质合成的比较研究。
Cold Spring Harb Symp Quant Biol. 1962;27:245-57. doi: 10.1101/sqb.1962.027.001.024.
7
Orotidylic acid decarboxylase: inhibition studies with azauridine 5'-phosphate.乳清苷酸脱羧酶:用5'-磷酸氮杂尿苷进行的抑制研究。
J Biol Chem. 1960 Oct;235:2917-9.
8
Propagation in tissue cultures of cytopathogenic agents from patients with measles.麻疹患者细胞病变病原体在组织培养中的传播。
Proc Soc Exp Biol Med. 1954 Jun;86(2):277-86. doi: 10.3181/00379727-86-21073.
9
Newcastle disease virus RNA. II. Preferential synthesis of RNA complementary to parental viral RNA by chick embryo cells.新城疫病毒核糖核酸。II. 鸡胚细胞优先合成与亲本病毒核糖核酸互补的核糖核酸。
J Mol Biol. 1966 Jun;18(1):204-14. doi: 10.1016/s0022-2836(66)80086-4.
10
Soluble antigen of measles virus.麻疹病毒可溶性抗原
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麻疹病毒核糖核酸与蛋白质合成:6-氮尿苷和环己酰亚胺对病毒复制的影响

Measles virus ribonucleic acid and protein synthesis: effects of 6-azauridine and cycloheximide on viral replication.

作者信息

Portner A, Bussell R H

出版信息

J Virol. 1973 Jan;11(1):46-53. doi: 10.1128/JVI.11.1.46-53.1973.

DOI:10.1128/JVI.11.1.46-53.1973
PMID:4630800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355059/
Abstract

Cycloheximide and 6-azauridine were employed to study the time course of measles virus protein and nucleic acid syntheses in AV3 cells. Synthesis of ribonucleic acid (RNA) essential for infectivity was first detected at 6 hr and increased concurrently with the formation of essential protein. Maximum levels of virus-specific RNA and protein were present by 18 hr, a time when only 5% of progeny virus was detected. Essential RNA and protein syntheses preceded the formation of infectious virus by at least 10 to 12 hr. The time course of RNA and protein syntheses essential for the formation of complement-fixing (CF) antigen and salt-dependent agglutinin (SDA) was also determined. RNA synthesis essential for the formation of SDA was first detected at 2 hr and was present maximally by 6 hr, whereas SDA-protein increased concurrently with the protein essential for infectivity. This suggested that the last protein essential for infectivity may be SDA. RNA synthesis essential for the formation of CF antigen was first detected at 4 hr, while CF-protein increased at 5 hr and preceded SDA-protein and protein essential for infectivity by approximately 3 hr. Reversal of inhibition of protein synthesis by cycloheximide indicated that early protein synthesis (1 to 3 hr) was required for the formation of infectious virus. The data suggest that the relatively long eclipse period observed with measles virus is related to a long maturation period rather than to late formation of early proteins, viral RNA, or structural proteins.

摘要

采用放线菌酮和6-氮尿苷研究了麻疹病毒在AV3细胞中蛋白质和核酸合成的时间进程。感染性必需的核糖核酸(RNA)合成在6小时首次检测到,并与必需蛋白质的形成同时增加。到18小时时出现病毒特异性RNA和蛋白质的最高水平,此时仅检测到5%的子代病毒。必需RNA和蛋白质合成比感染性病毒的形成至少提前10至12小时。还确定了补体结合(CF)抗原和盐依赖性凝集素(SDA)形成所必需的RNA和蛋白质合成的时间进程。SDA形成所必需的RNA合成在2小时首次检测到,并在6小时达到最大值,而SDA蛋白与感染性必需蛋白同时增加。这表明感染性必需的最后一种蛋白可能是SDA。CF抗原形成所必需的RNA合成在4小时首次检测到,而CF蛋白在5小时增加,比SDA蛋白和感染性必需蛋白提前约3小时。放线菌酮对蛋白质合成抑制作用的逆转表明,感染性病毒的形成需要早期蛋白质合成(1至3小时)。数据表明,麻疹病毒观察到的相对较长的隐蔽期与较长的成熟期有关,而不是与早期蛋白质、病毒RNA或结构蛋白的晚期形成有关。