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超螺旋DNA结构域拓扑组织的转变作为一种潜在的调控机制。

Transitions in topological organization of supercoiled DNA domains as a potential regulatory mechanism.

作者信息

Carnevali F, Caserta M, Di Mauro E

出版信息

J Biol Chem. 1984 Oct 25;259(20):12633-43.

PMID:6092340
Abstract

We present an analysis of the influence of DNA superhelicity on the topology of chimeric plasmids. A correlation is found between topological variations and in vivo/in vitro functions. Data refer to the topological transitions observed in function of variations of the superhelical density in the three closed DNA domains that represent the three extreme examples, from the point of view of the topological organization, among many chimeric systems analyzed. The plasmids studied are ADR2-BS-pBR322 (the vector pBR322 + the yeast gene ADR2), ADR3-5c-yRp7 (containing yeast TRP1, a constitutive mutant of yeast ADR2, a fragment of 5 kilobases of unanalyzed chromosomal DNA and the vector pBR322), and p31 (pBR322 + a yeast DNA fragment encompassing the right moiety of the Ty1 element and its in vivo promoter). In the model systems analyzed, the topological transitions observed in the eukaryotic sequences (relevant in one case for activation of selective in vitro transcription (Ty), in another (ADR2) for the in vivo expression) take place in the range of superhelical densities predicted on theoretical ground (Vologodskii, A. V., Lukashin, A. V. Anshelevich, V. V. & Frank-Kamenetskii, M. D. (1979) Nucleic Acids Res. 6, 967-982).

摘要

我们对DNA超螺旋对嵌合质粒拓扑结构的影响进行了分析。发现拓扑变化与体内/体外功能之间存在相关性。数据涉及在三个封闭DNA结构域中超螺旋密度变化的函数中观察到的拓扑转变,从拓扑组织的角度来看,这三个结构域代表了许多分析的嵌合系统中的三个极端例子。所研究的质粒有ADR2-BS-pBR322(载体pBR322 + 酵母基因ADR2)、ADR3-5c-yRp7(包含酵母TRP1、酵母ADR2的组成型突变体、5千碱基未分析的染色体DNA片段和载体pBR322)以及p31(pBR322 + 一个包含Ty1元件右半部分及其体内启动子的酵母DNA片段)。在所分析的模型系统中,在真核序列中观察到的拓扑转变(在一种情况下与选择性体外转录(Ty)的激活相关,在另一种情况下(ADR2)与体内表达相关)发生在理论预测的超螺旋密度范围内(沃洛戈茨基,A. V.,卢卡申,A. V.,安舍列维奇,V. V. & 弗兰克 - 卡缅涅茨基,M. D.(1979年)《核酸研究》6,967 - 982)。

相似文献

1
Transitions in topological organization of supercoiled DNA domains as a potential regulatory mechanism.超螺旋DNA结构域拓扑组织的转变作为一种潜在的调控机制。
J Biol Chem. 1984 Oct 25;259(20):12633-43.
2
Topological modifications and template activation are induced in chimaeric plasmids by inserted sequences.插入序列可诱导嵌合质粒发生拓扑修饰和模板激活。
J Mol Biol. 1983 Mar 25;165(1):59-77. doi: 10.1016/s0022-2836(83)80242-3.
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Yeast regulatory sequences preferentially adopt a non-B conformation in supercoiled DNA.酵母调控序列在超螺旋DNA中优先采用非B构象。
Nucleic Acids Res. 1987 Jun 11;15(11):4467-80. doi: 10.1093/nar/15.11.4467.
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Characterization of transposable element-associated mutations that alter yeast alcohol dehydrogenase II expression.改变酵母乙醇脱氢酶II表达的转座元件相关突变的特征分析。
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In vitro transcription of the yeast alcohol dehydrogenase I gene by homologous RNA polymerase B (II). Selective initiation and discontinuous elongation on a supercoiled template.酵母乙醇脱氢酶I基因由同源RNA聚合酶B(II)进行的体外转录。在超螺旋模板上的选择性起始和不连续延伸。
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In vitro generation of specific deletions in DNA cloned in M13 vectors using synthetic oligodeoxyribonucleotides: mutants in the 5'-flanking region of the yeast alcohol dehydrogenase II gene.利用合成寡脱氧核糖核苷酸在克隆于M13载体的DNA中体外产生特定缺失:酵母乙醇脱氢酶II基因5'侧翼区的突变体
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Cis-dominant regulatory mutations affecting the formation of glucose-repressible alcohol dehydrogenase (ADHII) in Saccharomyces cerevisiae.影响酿酒酵母中葡萄糖可抑制乙醇脱氢酶(ADHII)形成的顺式显性调控突变
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Transposable elements associated with constitutive expression of yeast alcohol dehydrogenase II.与酵母乙醇脱氢酶II组成型表达相关的转座元件
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Yeast RNA polymerase II transcription of circular DNA at different degrees of supercoiling.酵母RNA聚合酶II对不同超螺旋程度的环状DNA进行转录。
Nucleic Acids Res. 1982 Sep 11;10(17):5197-208. doi: 10.1093/nar/10.17.5197.
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Activation of in vitro transcription and topology of closed DNA domains.
J Biol Chem. 1985 Jan 10;260(1):152-9.

引用本文的文献

1
Histone H1 preferentially binds to superhelical DNA molecules of higher compaction.组蛋白H1优先结合更高压缩程度的超螺旋DNA分子。
Biophys J. 1997 Mar;72(3):1388-95. doi: 10.1016/S0006-3495(97)78785-X.
2
Histones H1 and H5 interact preferentially with crossovers of double-helical DNA.组蛋白H1和H5优先与双螺旋DNA的交叉点相互作用。
Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5052-6. doi: 10.1073/pnas.90.11.5052.
3
ADR1-mediated regulation of ADH2 requires an inverted repeat sequence.ADR1介导的ADH2调控需要一个反向重复序列。
Mol Cell Biol. 1986 Jun;6(6):1894-902. doi: 10.1128/mcb.6.6.1894-1902.1986.
4
Purified Saccharomyces cerevisiae RNA polymerase II interacts homologously with two different promoters as revealed by P1 endonuclease analysis.
Mol Gen Genet. 1986 Aug;204(2):249-57. doi: 10.1007/BF00425506.
5
Structure of RNA polymerase II promoters. Conformational alterations and template properties of circularized Saccharomyces cerevisiae GAL1-GAL10 divergent promoters.RNA聚合酶II启动子的结构。酿酒酵母GAL1 - GAL10双向启动子环化后的构象改变及模板特性。
EMBO J. 1986 Apr;5(4):763-71. doi: 10.1002/j.1460-2075.1986.tb04279.x.