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酵母URA3基因的高分辨率染色质结构为深入了解染色体环境中核小体的结构和定位提供了线索。

Chromatin structure of the yeast URA3 gene at high resolution provides insight into structure and positioning of nucleosomes in the chromosomal context.

作者信息

Tanaka S, Livingstone-Zatchej M, Thoma F

机构信息

Institut für Zellbiologie ETH-Hönggerberg, Zürich, Switzerland.

出版信息

J Mol Biol. 1996 Apr 19;257(5):919-34. doi: 10.1006/jmbi.1996.0212.

Abstract

To characterize nucleosome structure and positioning in the chromosomal context, the chromatin structure of the whole URA3 gene was studied in the genome and in a minichromosome by testing the accessibility of DNA to micrococcal nuclease and DNase I. The cutting patterns and hence the chromatin structures were almost indistinguishable in the genome and in the minichromosomes. The only notable exception was enhanced cutting between nucleosomes U3/U4 and U4/U5 in the minichromosomes. The results demonstrate that there is no severe constraint acting from outside the URA3 gene in chromosomes and minichromosomes. While low-resolution mapping showed six regions with a positioned nucleosome (U1 to U6), each region resolved in a complex pattern consistent with multiple overlapping positions. Some regions (U1, U4, U5 and U6) showed multiple positions with a dominant rotational setting (DNase I pattern), while U2 showed positioning within 10 bp but with no defined rotational setting, demonstrating that nucleosome positions were not in phase and not coordinately regulated. Reduced DNase I cutting from about 50 bp form the 5' end towards 3' end was common to all nucleosome regions. This polarity has been observed on isolated core particles. The results demonstrate that the DNase I pattern observed in vitro indeed reflects a structural property of nucleosomes in the chromosomal context. It is emphasized that despite the local heterogeneity revealed by high-resolution mapping, the low-resolution map is a reasonably accurate representation of the chromatin structure.

摘要

为了在染色体环境中表征核小体结构和定位,通过检测DNA对微球菌核酸酶和DNase I的可及性,研究了全URA3基因在基因组和微型染色体中的染色质结构。在基因组和微型染色体中,切割模式以及由此产生的染色质结构几乎无法区分。唯一显著的例外是微型染色体中核小体U3/U4和U4/U5之间的切割增强。结果表明,在染色体和微型染色体中,URA3基因外部没有严重的限制作用。虽然低分辨率图谱显示有六个区域存在定位核小体(U1至U6),但每个区域的解析结果都呈现出与多个重叠位置一致的复杂模式。一些区域(U1、U4、U5和U6)显示出多个具有主导旋转设置的位置(DNase I模式),而U2显示定位在10 bp范围内但没有明确的旋转设置,这表明核小体位置不同步且不受协调调节。从5'端向3'端约50 bp处DNase I切割减少在所有核小体区域中都很常见。这种极性在分离的核心颗粒上也有观察到。结果表明,体外观察到的DNase I模式确实反映了染色体环境中核小体的结构特性。需要强调的是,尽管高分辨率图谱揭示了局部异质性,但低分辨率图谱是染色质结构的合理准确表征。

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