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古菌核小体在体内和体外的定位是由一级序列基序决定的。

Archaeal nucleosome positioning in vivo and in vitro is directed by primary sequence motifs.

机构信息

Department of Molecular and Cellular Biochemistry, College of Medicine, University of Kentucky, Lexington, KY 40536, USA.

出版信息

BMC Genomics. 2013 Jun 10;14:391. doi: 10.1186/1471-2164-14-391.

Abstract

BACKGROUND

Histone wrapping of DNA into nucleosomes almost certainly evolved in the Archaea, and predates Eukaryotes. In Eukaryotes, nucleosome positioning plays a central role in regulating gene expression and is directed by primary sequence motifs that together form a nucleosome positioning code. The experiments reported were undertaken to determine if archaeal histone assembly conforms to the nucleosome positioning code.

RESULTS

Eukaryotic nucleosome positioning is favored and directed by phased helical repeats of AA/TT/AT/TA and CC/GG/CG/GC dinucleotides, and disfavored by longer AT-rich oligonucleotides. Deep sequencing of genomic DNA protected from micrococcal nuclease digestion by assembly into archaeal nucleosomes has established that archaeal nucleosome assembly is also directed and positioned by these sequence motifs, both in vivo in Methanothermobacter thermautotrophicus and Thermococcus kodakarensis and in vitro in reaction mixtures containing only one purified archaeal histone and genomic DNA. Archaeal nucleosomes assembled at the same locations in vivo and in vitro, with much reduced assembly immediately upstream of open reading frames and throughout the ribosomal rDNA operons. Providing further support for a common positioning code, archaeal histones assembled into nucleosomes on eukaryotic DNA and eukaryotic histones into nucleosomes on archaeal DNA at the same locations. T. kodakarensis has two histones, designated HTkA and HTkB, and strains with either but not both histones deleted grow normally but do exhibit transcriptome differences. Comparisons of the archaeal nucleosome profiles in the intergenic regions immediately upstream of genes that exhibited increased or decreased transcription in the absence of HTkA or HTkB revealed substantial differences but no consistent pattern of changes that would correlate directly with archaeal nucleosome positioning inhibiting or stimulating transcription.

CONCLUSIONS

The results obtained establish that an archaeal histone and a genome sequence together are sufficient to determine where archaeal nucleosomes preferentially assemble and where they avoid assembly. We confirm that the same nucleosome positioning code operates in Archaea as in Eukaryotes and presumably therefore evolved with the histone-fold mechanism of DNA binding and compaction early in the archaeal lineage, before the divergence of Eukaryotes.

摘要

背景

DNA 缠绕组蛋白形成核小体几乎肯定是在古菌中进化的,并且早于真核生物。在真核生物中,核小体定位在调节基因表达中起着核心作用,并由共同形成核小体定位密码的一级序列基序指导。进行这些实验是为了确定古菌组蛋白组装是否符合核小体定位密码。

结果

真核生物核小体定位受 AA/TT/AT/TA 和 CC/GG/CG/GC 二核苷酸相错的螺旋重复以及更长的富含 AT 的寡核苷酸的不利影响。通过对微球菌核酸酶消化保护的基因组 DNA 进行深度测序,发现古菌核小体组装也受这些序列基序的指导和定位,无论是在 Methanothermobacter thermautotrophicus 和 Thermococcus kodakarensis 中的体内,还是在仅含有一种纯化古菌组蛋白和基因组 DNA 的反应混合物中的体外。古菌核小体在体内和体外组装在相同的位置,在开放阅读框的上游和整个核糖体 rDNA 操纵子中组装明显减少。为共同的定位密码提供了进一步的支持,古菌组蛋白组装在真核生物 DNA 上形成核小体,而真核组蛋白组装在古菌 DNA 上形成核小体,位置相同。T. kodakarensis 有两种组蛋白,分别命名为 HTkA 和 HTkB,只有一种而不是两种组蛋白缺失的菌株生长正常,但确实表现出转录组差异。在 HTkA 或 HTkB 缺失时转录增加或减少的基因上游基因间区的古菌核小体图谱的比较显示出显著差异,但没有一致的变化模式,这与古菌核小体定位抑制或刺激转录直接相关。

结论

研究结果表明,古菌组蛋白和基因组序列一起足以确定古菌核小体优先组装的位置和避免组装的位置。我们证实,在古菌中与在真核生物中一样,相同的核小体定位密码起作用,并且可能因此在真核生物分化之前,在古菌谱系中与组蛋白折叠机制一起进化,与 DNA 结合和压缩有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b34/3691661/e559cf553447/1471-2164-14-391-1.jpg

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