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延伸的 RNA 聚合酶 II 复合物在转录基因座中的均匀分布。

Uniform distribution of elongating RNA polymerase II complexes in transcribed gene locus.

机构信息

Institute of Molecular and Cell Biology, University of Tartu, Riia 23, Tartu 51010, Estonia.

出版信息

J Biol Chem. 2011 Jul 8;286(27):23817-22. doi: 10.1074/jbc.M111.230805. Epub 2011 May 23.

Abstract

The intensity of gene transcription is generally reflected by the level of RNA polymerase II (RNAPII) recruitment to the gene. However, genome-wide studies of polymerase occupancy indicate that RNAPII distribution varies among genes. In some loci more polymerases are found in the 5' region, whereas in other loci, in the 3' region of the gene. We studied the distribution of elongating RNAPII complexes at highly transcribed GAL-VPS13 locus in Saccharomyces cerevisiae and found that in the cell population the amount of polymerases gradually decreased toward the 3' end of the gene. However, the conventional chromatin immunoprecipitation assay averages the signal from the cell population, and no data on single cell level can be gathered. To study the spacing of elongating polymerases on single chromosomes, we used a sequential chromatin immunoprecipitation assay for the detection of multiple RNAPII complexes on the same DNA fragment. Our results demonstrate uniform distribution of elongating polymerases throughout all regions of the GAL-VPS13 gene.

摘要

基因转录的强度通常反映了 RNA 聚合酶 II(RNAPII)向基因募集的水平。然而,聚合酶占据的全基因组研究表明,RNAPII 的分布在基因之间存在差异。在一些基因座中,更多的聚合酶存在于 5'区域,而在其他基因座中,聚合酶存在于基因的 3'区域。我们研究了在酿酒酵母中高度转录的 GAL-VPS13 基因座中延伸的 RNAPII 复合物的分布,发现聚合酶的数量在细胞群体中逐渐向基因的 3'端减少。然而,传统的染色质免疫沉淀测定法平均了细胞群体的信号,无法收集到单细胞水平的数据。为了研究单个染色体上延伸聚合酶的间隔,我们使用了一种连续的染色质免疫沉淀测定法,用于检测同一 DNA 片段上的多个 RNAPII 复合物。我们的结果表明,延伸聚合酶在 GAL-VPS13 基因的所有区域均匀分布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ac/3129163/6669949dc3f7/zbc0341170890001.jpg

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