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痘苗病毒感染HeLa细胞诱导的两类DNA的从头合成。

De novo synthesis of two classes of DNA induced by vaccinia virus infection of HeLa cells.

作者信息

Archard L C

出版信息

J Gen Virol. 1979 Jan;42(1):223-9. doi: 10.1099/0022-1317-42-1-223.

Abstract

Equilibrium density gradient centrifugation in CsCl confirms that DNA synthesized after vaccinia virus infection of HeLa cells is homogeneous in buoyant density and thus in base composition and is similar in this respect to bulk HeLa cell DNA. In contrast, rate sedimentation in alkaline sucrose gradients distinguishes two main classes of virus-induced DNA, neither of which can be equated with cell DNA synthesized in the same cultures prior to infection. The slower sedimenting class of virus-induced DNA co-sediments with DNA from purified virus particles: the second class sediments faster than pre-labelled cell DNA. Heterogeneity of virus-induced DNA does not result from fragmentation of radioactively labelled DNA, virus-mediated breakdown of cell DNA or association with either proteins or polyamines. Both slow and fast sedimenting classes of virus-induced DNA contain sequences complementary to all restriction endonuclease Hind III-specific fragments of the virus genome. The multiple species of DNA synthesized after infection are distinguished further by the effect of ethidium bromide. At a concentration which prevents the formation of infectious progeny virus, this compound inhibits selectively the de novo synthesis of that class of virus-induced DNA which sediments faster in alkaline sucrose gradients.

摘要

在氯化铯中进行平衡密度梯度离心证实,在痘苗病毒感染HeLa细胞后合成的DNA在浮力密度上是均匀的,因此在碱基组成上也是均匀的,并且在这方面与HeLa细胞的总DNA相似。相比之下,在碱性蔗糖梯度中的速率沉降区分出两类主要的病毒诱导DNA,其中任何一类都不能等同于感染前在相同培养物中合成的细胞DNA。病毒诱导DNA中沉降较慢的一类与纯化病毒颗粒中的DNA共同沉降:第二类沉降速度比预先标记的细胞DNA快。病毒诱导DNA的异质性并非源于放射性标记DNA的片段化、病毒介导的细胞DNA分解或与蛋白质或多胺的结合。病毒诱导DNA中沉降慢和快的两类都含有与病毒基因组所有限制性内切酶Hind III特异性片段互补的序列。感染后合成的多种DNA通过溴化乙锭的作用进一步区分。在防止产生有感染性的子代病毒的浓度下,这种化合物选择性地抑制在碱性蔗糖梯度中沉降较快的那类病毒诱导DNA的从头合成。

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