核小体定位。

ISRN molecular biology Pub Date : 2012-10-15 eCollection Date: 2012-01-01 DOI:10.5402/2012/245706
Hiromi Nishida
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引用次数: 3

摘要

核小体定位不仅与基因组DNA的压缩有关,还与其他生物学功能有关。在染色质被微球菌核酸酶消化后,可以对核小体(核小体结合)DNA片段进行测序并将其绘制到基因组DNA序列上。由于现代DNA测序技术的发展,全基因组核小体作图已经在广泛的真核生物物种中进行。对核小体位置的比较分析表明,核小体在外显子区域比在内含子区域更频繁地形成,并且大多数转录起始和翻译(或转录)结束位点位于核小体连接子DNA区域,这表明核小体的定位影响转录起始、转录终止和基因剪接。此外,核小体DNA含有丰富的鸟嘌呤和胞嘧啶(G + C)序列以及高水平的胞嘧啶甲基化。因此,核小体定位系统在真核生物进化过程中是保守的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nucleosome Positioning.

Nucleosome Positioning.

Nucleosome Positioning.

Nucleosome positioning is not only related to genomic DNA compaction but also to other biological functions. After the chromatin is digested by micrococcal nuclease, nucleosomal (nucleosome-bound) DNA fragments can be sequenced and mapped on the genomic DNA sequence. Due to the development of modern DNA sequencing technology, genome-wide nucleosome mapping has been performed in a wide range of eukaryotic species. Comparative analyses of the nucleosome positions have revealed that the nucleosome is more frequently formed in exonic than intronic regions, and that most of transcription start and translation (or transcription) end sites are located in nucleosome linker DNA regions, indicating that nucleosome positioning influences transcription initiation, transcription termination, and gene splicing. In addition, nucleosomal DNA contains guanine and cytosine (G + C)-rich sequences and a high level of cytosine methylation. Thus, the nucleosome positioning system has been conserved during eukaryotic evolution.

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