Suter B, Schnappauf G, Thoma F
Institut für Zellbiologie, ETH-Zürich, Hönggerberg, CH-8093 Zürich, Switzerland.
Nucleic Acids Res. 2000 Nov 1;28(21):4083-9. doi: 10.1093/nar/28.21.4083.
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.
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。