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本文引用的文献

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Destabilization of nucleosomes by an unusual DNA conformation adopted by poly(dA) small middle dotpoly(dT) tracts in vivo.体内聚(dA)·聚(dT)片段所采用的异常DNA构象导致核小体不稳定。
EMBO J. 2000 Jul 3;19(13):3358-65. doi: 10.1093/emboj/19.13.3358.
2
DNA repair in a yeast origin of replication: contributions of photolyase and nucleotide excision repair.酵母复制起点处的DNA修复:光解酶和核苷酸切除修复的作用
Nucleic Acids Res. 2000 May 15;28(10):2060-8. doi: 10.1093/nar/28.10.2060.
3
Different roles for abf1p and a T-rich promoter element in nucleosome organization of the yeast RPS28A gene.abf1p和富含T的启动子元件在酵母RPS28A基因核小体组织中的不同作用。
Nucleic Acids Res. 2000 Mar 15;28(6):1390-6. doi: 10.1093/nar/28.6.1390.
4
Light and dark in chromatin repair: repair of UV-induced DNA lesions by photolyase and nucleotide excision repair.染色质修复中的光与暗:光裂合酶和核苷酸切除修复对紫外线诱导的DNA损伤的修复
EMBO J. 1999 Dec 1;18(23):6585-98. doi: 10.1093/emboj/18.23.6585.
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Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome.核小体的二十五年,真核生物染色体的基本颗粒
Cell. 1999 Aug 6;98(3):285-94. doi: 10.1016/s0092-8674(00)81958-3.
6
TATA-binding protein promotes the selective formation of UV-induced (6-4)-photoproducts and modulates DNA repair in the TATA box.TATA 结合蛋白促进紫外线诱导的(6-4)光产物的选择性形成,并调节 TATA 框中的 DNA 修复。
EMBO J. 1999 Jan 15;18(2):433-43. doi: 10.1093/emboj/18.2.433.
7
Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction.酵母SAGA复合物的功能组织:参与结构完整性、核小体乙酰化及TATA结合蛋白相互作用的不同组分
Mol Cell Biol. 1999 Jan;19(1):86-98. doi: 10.1128/MCB.19.1.86.
8
Alteration of nucleosome structure as a mechanism of transcriptional regulation.核小体结构改变作为转录调控的一种机制。
Annu Rev Biochem. 1998;67:545-79. doi: 10.1146/annurev.biochem.67.1.545.
9
Distinct frequency-distributions of homopolymeric DNA tracts in different genomes.不同基因组中同聚物DNA序列的独特频率分布。
Nucleic Acids Res. 1998 Sep 1;26(17):4056-62. doi: 10.1093/nar/26.17.4056.
10
Datin, a yeast poly(dA:dT)-binding protein, behaves as an activator of the wild-type ILV1 promoter and interacts synergistically with Reb1p.达汀是一种酵母多聚(dA:dT)结合蛋白,它作为野生型ILV1启动子的激活剂,并与Reb1p协同相互作用。
Mol Gen Genet. 1998 Apr;258(1-2):95-103. doi: 10.1007/s004380050711.

在体内无核小体的酵母启动子中,聚(dA.dT)序列以刚性DNA结构存在。

Poly(dA.dT) sequences exist as rigid DNA structures in nucleosome-free yeast promoters in vivo.

作者信息

Suter B, Schnappauf G, Thoma F

机构信息

Institut für Zellbiologie, ETH-Zürich, Hönggerberg, CH-8093 Zürich, Switzerland.

出版信息

Nucleic Acids Res. 2000 Nov 1;28(21):4083-9. doi: 10.1093/nar/28.21.4083.

DOI:10.1093/nar/28.21.4083
PMID:11058103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC113125/
Abstract

Poly(dA.dT) sequences (T-tracts) are abundant genomic DNA elements with unusual properties in vitro and an established role in transcriptional regulation of yeast genes. In vitro T-tracts are rigid, contribute to DNA bending, affect assembly in nucleosomes and generate a characteristic pattern of CPDs (cyclobutane pyrimidine dimers) upon irradiation with UV light (UV photofootprint). In eukaryotic cells, where DNA is packaged in chromatin, the DNA structure of T-tracts is unknown. Here we have used in vivo UV photofootprinting and DNA repair by photolyase to investigate the structure and accessibility of T-tracts in yeast promoters (HIS3, URA3 and ILV1). The same characteristic photofootprints were obtained in yeast and in naked DNA, demonstrating that the unusual T-tract structure exists in living cells. Rapid repair of CPDs in the T-tracts demonstrates that these T-tracts were not folded in nucleosomes. Moreover, neither datin, a T-tract binding protein, nor Gcn5p, a histone acetyltransferase involved in nucleosome remodelling, showed an influence on the structure and accessibility of T-tracts. The data support a contribution of this unusual DNA structure to transcriptional regulation.

摘要

聚(dA.dT)序列(T序列)是丰富的基因组DNA元件,在体外具有不同寻常的特性,并且在酵母基因的转录调控中发挥着既定作用。体外的T序列是刚性的,有助于DNA弯曲,影响核小体的组装,并在紫外线照射时产生特征性的环丁烷嘧啶二聚体(CPD)模式(紫外线光足迹)。在DNA包装在染色质中的真核细胞中,T序列的DNA结构尚不清楚。在这里,我们利用体内紫外线光足迹法和光解酶进行DNA修复,来研究酵母启动子(HIS3、URA3和ILV1)中T序列的结构和可及性。在酵母和裸露DNA中获得了相同的特征性光足迹,表明这种不同寻常的T序列结构存在于活细胞中。T序列中CPD的快速修复表明这些T序列没有折叠在核小体中。此外,T序列结合蛋白达汀(datin)和参与核小体重塑的组蛋白乙酰转移酶Gcn5p,均未对T序列的结构和可及性产生影响。这些数据支持了这种不同寻常的DNA结构对转录调控的作用。