首页> 外文期刊>Journal of Molecular Biology >CHROMATIN STRUCTURE OF THE YEAST URA3 GENE AT HIGH RESOLUTION PROVIDES INSIGHT INTO STRUCTURE AND POSITIONING OF NUCLEOSOMES IN THE CHROMOSOMAL CONTEXT
【24h】

CHROMATIN STRUCTURE OF THE YEAST URA3 GENE AT HIGH RESOLUTION PROVIDES INSIGHT INTO STRUCTURE AND POSITIONING OF NUCLEOSOMES IN THE CHROMOSOMAL CONTEXT

机译:高分辨率的酵母URA3基因的染色质结构提供了染色体上下文中核糖体结构和定位的信息

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

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 minichromomes. 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. (C) 1996 Academic Press Limited [References: 58]
机译:为了表征核小体的结构和在染色体背景中的定位,通过测试DNA与微球菌核酸酶和DNase I的可及性,研究了整个URA3基因在染色体和微型染色体中的染色质结构。切割模式和染色质结构为在基因组和微染色体中几乎没有区别。唯一值得注意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,在染色体和微染色体中,没有来自URA3基因外部的严格限制。低分辨率作图显示六个区域具有定位的核小体(U1至U6),每个区域以复杂的模式解析,与多个重叠位置一致。一些区域(U1,U4,U5和U6)显示出多个位置,并具有显着的旋转设置(DNase I模式),而U2显示了位于10 bp以内的位置,但没有定义的旋转设置,表明核小体位置不在同相且不协调规范的。从5'端到3'端的大约50 bp的DNase I切割减少对于所有核小体区域都是常见的。在分离的核颗粒上已经观察到这种极性。结果表明,体外观察到的DNase I模式确实反映了染色体背景下核小体的结构特性。要强调的是,尽管高分辨率映射揭示了局部异质性,但低分辨率映射是染色质结构的合理准确表示。 (C)1996 Academic Press Limited [参考号:58]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号