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1
Deletion mapping a eukaryotic promoter.真核生物启动子的缺失作图
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4461-5. doi: 10.1073/pnas.78.7.4461.
2
The yeast his3 promoter contains at least two distinct elements.酵母his3启动子至少包含两个不同的元件。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7385-9. doi: 10.1073/pnas.79.23.7385.
3
Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast.天然存在的聚(dA-dT)序列是酵母中组成型转录的上游启动子元件。
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8419-23. doi: 10.1073/pnas.82.24.8419.
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Genetic properties and chromatin structure of the yeast gal regulatory element: an enhancer-like sequence.酵母半乳糖调节元件的遗传特性和染色质结构:一个类似增强子的序列。
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Nucleotide sequence and transcriptional mapping of the yeast pet56-his3-ded1 gene region.酵母pet56-his3-ded1基因区域的核苷酸序列及转录图谱
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Two related regulatory sequences are required for maximal induction of Saccharomyces cerevisiae his3 transcription.酿酒酵母his3转录的最大诱导需要两个相关的调控序列。
Mol Cell Biol. 1987 Jan;7(1):104-10. doi: 10.1128/mcb.7.1.104-110.1987.
7
Yeast HIS3 expression in Escherichia coli depends upon fortuitous homology between eukaryotic and prokaryotic promoter elements.酵母HIS3基因在大肠杆菌中的表达取决于真核和原核启动子元件之间的偶然同源性。
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Promotor mutants of the yeast his3 gene.酵母组氨酸3基因的启动子突变体
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引用本文的文献

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What history tells us XXXV. Enhancers: their existence and characteristics have raised puzzling issues since their discovery.历史告诉我们XXXV. 增强子:自发现以来,它们的存在和特性引发了诸多令人困惑的问题。
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Plasmid cloning and expression of the E. coli polA (+) gene in S. cerevisiae.在酿酒酵母中克隆和表达大肠杆菌 polA(+)基因的质粒。
Curr Genet. 1984 Jul;8(5):333-40. doi: 10.1007/BF00419821.
3
Sequences upstream from the T-A-T-A box are required in vivo and in vitro for efficient transcription from the adenovirus serotype 2 major late promoter.腺病毒2型主要晚期启动子在体内和体外进行有效转录时,需要T-A-T-A框上游的序列。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7132-6. doi: 10.1073/pnas.79.23.7132.
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The yeast his3 promoter contains at least two distinct elements.酵母his3启动子至少包含两个不同的元件。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7385-9. doi: 10.1073/pnas.79.23.7385.
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Immunochemical study of chromatin non-histone proteins. II. Localization of immunogenic tissue-specific proteins in nuclease-hypersensitive sites of chromatin.染色质非组蛋白的免疫化学研究。II. 免疫原性组织特异性蛋白在染色质核酸酶超敏位点中的定位。
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Participation of transcriptional and post-transcriptional regulatory mechanisms in the control of arginine metabolism in yeast.转录和转录后调控机制在酵母精氨酸代谢控制中的作用。
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Adenovirus 5 E2 transcription unit: an E1A-inducible promoter with an essential element that functions independently of position or orientation.腺病毒5型E2转录单元:一个E1A诱导型启动子,带有一个独立于位置或方向发挥作用的必需元件。
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9
Elastic torsional strain in DNA within a fraction of SV40 minichromosomes: relation to transcriptionally active chromatin.SV40 微型染色体片段内 DNA 的弹性扭转应变:与转录活性染色质的关系。
EMBO J. 1982;1(11):1353-8. doi: 10.1002/j.1460-2075.1982.tb01322.x.
10
Transcription of a cloned Xenopus laevis H4 histone gene in the homologous frog oocyte system depends on an evolutionary conserved sequence motif in the -50 region.克隆的非洲爪蟾H4组蛋白基因在同源蛙卵母细胞系统中的转录依赖于-50区域的一个进化保守序列基序。
Nucleic Acids Res. 1983 Dec 20;11(24):8641-57. doi: 10.1093/nar/11.24.8641.

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GENE-ENZYME RELATIONS IN HISTIDINE BIOSYNTHESIS IN YEAST.酵母中组氨酸生物合成的基因-酶关系
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[THE PROMOTOR, A GENETIC ELEMENT NECESSARY TO THE EXPRESSION OF AN OPERON].[启动子,操纵子表达所必需的遗传元件]
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Identification of regulatory sequences in the prelude sequences of an H2A histone gene by the study of specific deletion mutants in vivo.通过对体内特定缺失突变体的研究鉴定H2A组蛋白基因前奏序列中的调控序列。
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Gene regulation at the right operator (OR) of bacteriophage lambda. III. lambda repressor directly activates gene transcription.λ噬菌体右操纵基因(OR)处的基因调控。III. λ阻遏物直接激活基因转录。
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A physiological study of functional expression in Escherichia coli of the cloned yeast imidazoleglycerolphosphate dehydratase gene.克隆的酵母咪唑甘油磷酸脱水酶基因在大肠杆菌中功能表达的生理学研究。
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In vivo sequence requirements of the SV40 early promotor region.猴空泡病毒40早期启动子区域的体内序列要求
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Deletions covering the putative promoter region of early mRNAs of simian virus 40 do not abolish T-antigen expression.覆盖猴病毒40早期mRNA推定启动子区域的缺失不会消除T抗原的表达。
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Promoter sequences of eukaryotic protein-coding genes.真核生物蛋白质编码基因的启动子序列。
Science. 1980 Sep 19;209(4463):1406-14. doi: 10.1126/science.6251548.
9
Regulatory mutants of polyoma virus defective in DNA replication and the synthesis of early proteins.在DNA复制和早期蛋白质合成方面存在缺陷的多瘤病毒调节突变体。
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E. coli RNA polymerase interacts homologously with two different promoters.大肠杆菌RNA聚合酶与两种不同的启动子进行同源性相互作用。
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真核生物启动子的缺失作图

Deletion mapping a eukaryotic promoter.

作者信息

Struhl K

出版信息

Proc Natl Acad Sci U S A. 1981 Jul;78(7):4461-5. doi: 10.1073/pnas.78.7.4461.

DOI:10.1073/pnas.78.7.4461
PMID:7027262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC319811/
Abstract

The phenotypes of 24 mutants that successively delete DNA sequences adjacent to the 5' end of the Saccharomyces cerevisiae (yeast) his3 structural gene are described. Deletions retaining greater than 155 base pairs before the mRNA coding sequences are phenotypically indistinguishable from the wild-type his3 allele. Deletions having end points between 113 and 65 base pairs before the transcription initiation site express his3 at reduced levels. Mutations retaining less than 45 base pairs are indistinguishable from null alleles of the his3 locus. These results indicate (i) that a sequence(s) located 113--155 base pairs upstream from the transcribed region is necessary for wild-type expression and (ii) that the T-A-T-A box (a sequence in front of most eukaryotic genes) is not sufficient for wild-type promoter function. Thus, the yeast his3 promoter region appears large when compared with prokaryotic promoters, suggesting that it may be more complex than a simple site of interaction between RNA polymerase and DNA.

摘要

本文描述了24个连续缺失酿酒酵母(酵母)his3结构基因5'端相邻DNA序列的突变体的表型。在mRNA编码序列之前保留大于155个碱基对的缺失在表型上与野生型his3等位基因无法区分。在转录起始位点之前113至65个碱基对之间具有端点的缺失以降低的水平表达his3。保留少于45个碱基对的突变与his3基因座的无效等位基因无法区分。这些结果表明:(i)位于转录区域上游113 - 155个碱基对的一个或多个序列对于野生型表达是必需的;(ii)T - A - T - A框(大多数真核基因前面的一个序列)对于野生型启动子功能是不够的。因此,与原核生物启动子相比,酵母his3启动子区域显得很大,这表明它可能比RNA聚合酶与DNA之间简单的相互作用位点更复杂。