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溴脱氧尿苷诱导的豚鼠病毒的生化特性。

Biochemical properties of the bromodeoxyuridine-induced guinea pig virus.

作者信息

Michalides R, Schlom J, Dahlberg J, Perk K

出版信息

J Virol. 1975 Oct;16(4):1039-50. doi: 10.1128/JVI.16.4.1039-1050.1975.

Abstract

The biophysical and biochemical properties of the virus particles released by guinea pig embryo cells treated with 5-bromo-2'-deoxyuridine (BUdR) have been compared to those of the B-type mouse mammary tumor virus (MMTV) and the C-type Rauscher murine leukemia virus. The high-molecular-weight (60 to 70S) RNA of the BUdR-induced guinea pig virus (GPV) has a molecular weight of 8 X 106 when measred by mixed agarose polyacylamide gel electrophoresis. The virus particles isolated from the tissue culture medium of BUdR-induced guniea pig cells have the following properties in common with MMTV: (i) a buoyant density of 1.18 g/ml in sucrose and 1.21 g/ml in CsCl, and (ii) a DNA polymerase that prefers Mg2+ over Mn2+ in an assay using the synthetic template poly(rC):oligo(dG). No nucleic acid sequence homology between GPV RNA and the viral RNAs of the MMTV, murine leukemia virus, hamster sarcoma virus, or Mason-Pfizer monkey virus could be observed in a competition hybridization assay using the radioactive-labeled GPV 60 to 70S RNA. By this same competition by hybridization assay the frequency of GPV proviral sequences was estimated to be at least 83 per haploid cellular genome of guniea pig cells. No nucleic acid sequences related to be GPV RNA were detected in the DNA of normal tissues of mice, rats, cats, dogs, baboons, or humans by direct RNA-DNA hybridization using radioactive GPV60 to 70S RNA.

摘要

用5-溴-2'-脱氧尿苷(BUdR)处理的豚鼠胚胎细胞释放的病毒颗粒的生物物理和生化特性,已与B型小鼠乳腺肿瘤病毒(MMTV)和C型劳氏鼠白血病病毒的特性进行了比较。通过混合琼脂糖聚丙烯酰胺凝胶电泳测量,BUdR诱导的豚鼠病毒(GPV)的高分子量(60至70S)RNA分子量为8×10⁶ 。从BUdR诱导的豚鼠细胞的组织培养基中分离出的病毒颗粒与MMTV具有以下共同特性:(i)在蔗糖中的浮力密度为1.18 g/ml,在CsCl中的浮力密度为1.21 g/ml,以及(ii)在使用合成模板聚(rC):寡聚(dG)的测定中,一种优先选择Mg²⁺ 而非Mn²⁺ 的DNA聚合酶。在使用放射性标记的GPV 60至70S RNA的竞争杂交试验中,未观察到GPV RNA与MMTV、鼠白血病病毒、仓鼠肉瘤病毒或梅森 - Pfizer猴病毒的病毒RNA之间的核酸序列同源性。通过相同的竞争杂交试验,估计GPV前病毒序列在豚鼠细胞的每个单倍体细胞基因组中的频率至少为83。通过使用放射性GPV60至70S RNA的直接RNA - DNA杂交,在小鼠、大鼠、猫、狗、狒狒或人类的正常组织DNA中未检测到与GPV RNA相关的核酸序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab6/354766/0a5ca48f0160/jvirol00238-0299-a.jpg

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