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来自未感染的海拉细胞的RNA可刺激腺病毒DNA在体外的复制。

Adenovirus DNA replication in vitro is stimulated by RNA from uninfected HeLa cells.

作者信息

van der Vliet P C, van Dam D, Kwant M M

出版信息

FEBS Lett. 1984 Jun 4;171(1):5-8. doi: 10.1016/0014-5793(84)80449-4.

DOI:10.1016/0014-5793(84)80449-4
PMID:6723975
Abstract

Adenovirus DNA replication was studied in a partially reconstituted system consisting of purified viral proteins (DNA-binding protein, precursor terminal protein and Ad DNA polymerase) and a nuclear extract from uninfected HeLa cells. Optimal DNA replication required the presence of a heat-stable, ribonuclease-sensitive fraction from the cytosol of uninfected cells. This fraction stimulated the initiation about 3-fold and the replication of origin fragments 5-10-fold. Sedimentation analysis indicated the presence of a fast-sedimenting and a slow-sedimenting component which complemented each other. At least part of the stimulation was caused by low-molecular-mass RNA.

摘要

在一个部分重构的系统中研究了腺病毒DNA复制,该系统由纯化的病毒蛋白(DNA结合蛋白、前体末端蛋白和腺病毒DNA聚合酶)以及来自未感染的HeLa细胞的核提取物组成。最佳的DNA复制需要存在来自未感染细胞胞质溶胶的热稳定、核糖核酸酶敏感部分。该部分将起始反应刺激约3倍,将起始片段的复制刺激5至10倍。沉降分析表明存在相互补充的快速沉降和慢速沉降成分。至少部分刺激是由低分子量RNA引起的。

相似文献

1
Adenovirus DNA replication in vitro is stimulated by RNA from uninfected HeLa cells.来自未感染的海拉细胞的RNA可刺激腺病毒DNA在体外的复制。
FEBS Lett. 1984 Jun 4;171(1):5-8. doi: 10.1016/0014-5793(84)80449-4.
2
Template activating factor I, a novel host factor required to stimulate the adenovirus core DNA replication.模板激活因子I,一种刺激腺病毒核心DNA复制所需的新型宿主因子。
J Biol Chem. 1993 May 15;268(14):10582-7.
3
Replication of adenovirus DNA-protein complex with purified proteins.用纯化蛋白对腺病毒DNA-蛋白质复合物进行复制。
Proc Natl Acad Sci U S A. 1981 Feb;78(2):884-8. doi: 10.1073/pnas.78.2.884.
4
In vitro complementation as an assay for purification of adenovirus DNA replication proteins.体外互补作为腺病毒DNA复制蛋白纯化的一种检测方法。
Proc Natl Acad Sci U S A. 1983 Feb;80(4):935-9. doi: 10.1073/pnas.80.4.935.
5
DNA sequences required for the in vitro replication of adenovirus DNA.腺病毒DNA体外复制所需的DNA序列。
Proc Natl Acad Sci U S A. 1984 May;81(10):3069-73. doi: 10.1073/pnas.81.10.3069.
6
Replication of adenovirus type 4 DNA by a purified fraction from infected cells.通过来自受感染细胞的纯化组分对4型腺病毒DNA进行复制。
Nucleic Acids Res. 1991 Jun 25;19(12):3243-9. doi: 10.1093/nar/19.12.3243.
7
Mechanism of inhibition of adenovirus DNA replication by the acyclic nucleoside triphosphate analogue (S)-HPMPApp: influence of the adenovirus DNA binding protein.无环核苷三磷酸类似物(S)-HPMPApp对腺病毒DNA复制的抑制机制:腺病毒DNA结合蛋白的影响
Nucleic Acids Res. 1989 Nov 25;17(22):8917-29. doi: 10.1093/nar/17.22.8917.
8
Adenovirus DNA replication in a reconstituted system.腺病毒DNA在重组系统中的复制。
Methods Enzymol. 1995;262:548-60. doi: 10.1016/0076-6879(95)62044-3.
9
Adenovirus subviral particles and cores can support limited DNA replication.
J Gen Virol. 1989 Dec;70 ( Pt 12):3235-48. doi: 10.1099/0022-1317-70-12-3235.
10
Sequence-specific interactions between cellular DNA-binding proteins and the adenovirus origin of DNA replication.细胞DNA结合蛋白与腺病毒DNA复制起点之间的序列特异性相互作用。
Mol Cell Biol. 1987 Feb;7(2):875-86. doi: 10.1128/mcb.7.2.875-886.1987.

引用本文的文献

1
Recognition site of nuclear factor I, a sequence-specific DNA-binding protein from HeLa cells that stimulates adenovirus DNA replication.核因子I的识别位点,一种来自HeLa细胞的序列特异性DNA结合蛋白,可刺激腺病毒DNA复制。
EMBO J. 1985 Jun;4(6):1515-21. doi: 10.1002/j.1460-2075.1985.tb03811.x.
2
Adenovirus DNA replication in vitro: site-directed mutagenesis of the nuclear factor I binding site of the Ad2 origin.腺病毒DNA的体外复制:腺病毒2型起源的核因子I结合位点的定点诱变
Nucleic Acids Res. 1985 Jul 11;13(13):4935-52. doi: 10.1093/nar/13.13.4935.
3
Functional homology between the sequence-specific DNA-binding proteins nuclear factor I from HeLa cells and the TGGCA protein from chicken liver.
来自HeLa细胞的序列特异性DNA结合蛋白核因子I与来自鸡肝的TGGCA蛋白之间的功能同源性。
EMBO J. 1986 Feb;5(2):381-6. doi: 10.1002/j.1460-2075.1986.tb04223.x.
4
Mechanism of inhibition of adenovirus DNA replication by the acyclic nucleoside triphosphate analogue (S)-HPMPApp: influence of the adenovirus DNA binding protein.无环核苷三磷酸类似物(S)-HPMPApp对腺病毒DNA复制的抑制机制:腺病毒DNA结合蛋白的影响
Nucleic Acids Res. 1989 Nov 25;17(22):8917-29. doi: 10.1093/nar/17.22.8917.