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酵母中的全基因组核小体占据情况。

Global nucleosome occupancy in yeast.

作者信息

Bernstein Bradley E, Liu Chih Long, Humphrey Emily L, Perlstein Ethan O, Schreiber Stuart L

机构信息

Department of Chemistry and Chemical Biology, Bauer Center for Genomics Research, and Howard Hughes Medical Institute, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA.

出版信息

Genome Biol. 2004;5(9):R62. doi: 10.1186/gb-2004-5-9-r62. Epub 2004 Aug 20.

Abstract

BACKGROUND

Although eukaryotic genomes are generally thought to be entirely chromatin-associated, the activated PHO5 promoter in yeast is largely devoid of nucleosomes. We systematically evaluated nucleosome occupancy in yeast promoters by immunoprecipitating nucleosomal DNA and quantifying enrichment by microarrays.

RESULTS

Nucleosome depletion is observed in promoters that regulate active genes and/or contain multiple evolutionarily conserved motifs that recruit transcription factors. The Rap1 consensus was the only binding motif identified in a completely unbiased search of nucleosome-depleted promoters. Nucleosome depletion in the vicinity of Rap1 consensus sites in ribosomal protein gene promoters was also observed by real-time PCR and micrococcal nuclease digestion. Nucleosome occupancy in these regions was increased by the small molecule rapamycin or, in the case of the RPS11B promoter, by removing the Rap1 consensus sites.

CONCLUSIONS

The presence of transcription factor-binding motifs is an important determinant of nucleosome depletion. Most motifs are associated with marked depletion only when they appear in combination, consistent with a model in which transcription factors act collaboratively to exclude nucleosomes and gain access to target sites in the DNA. In contrast, Rap1-binding sites cause marked depletion under steady-state conditions. We speculate that nucleosome depletion enables Rap1 to define chromatin domains and alter them in response to environmental cues.

摘要

背景

尽管真核生物基因组通常被认为完全与染色质相关,但酵母中激活的PHO5启动子在很大程度上没有核小体。我们通过免疫沉淀核小体DNA并用微阵列定量富集,系统地评估了酵母启动子中的核小体占据情况。

结果

在调控活跃基因和/或含有多个招募转录因子的进化保守基序的启动子中观察到核小体缺失。Rap1共有序列是在对核小体缺失启动子进行完全无偏搜索中鉴定出的唯一结合基序。通过实时PCR和微球菌核酸酶消化,也观察到核糖体蛋白基因启动子中Rap1共有序列位点附近的核小体缺失。这些区域中的核小体占据情况因小分子雷帕霉素而增加,或者对于RPS11B启动子而言,通过去除Rap1共有序列位点而增加。

结论

转录因子结合基序的存在是核小体缺失的重要决定因素。大多数基序仅在它们组合出现时才与明显的缺失相关,这与一种模型一致,即转录因子协同作用以排除核小体并获得对DNA中靶位点的访问。相反,Rap1结合位点在稳态条件下导致明显的缺失。我们推测核小体缺失使Rap1能够定义染色质结构域并根据环境线索改变它们。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93f5/522869/83d539d25c4c/gb-2004-5-9-r62-1.jpg

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