Fischer Jenny J, Toedling Joern, Krueger Tammo, Schueler Markus, Huber Wolfgang, Sperling Silke
Department of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Ihnestrasse 73, 14195 Berlin, Germany.
Genomics. 2008 Jan;91(1):41-51. doi: 10.1016/j.ygeno.2007.08.010. Epub 2007 Nov 8.
Nucleosomes are involved in DNA compaction and transcriptional regulation. Yet it is unclear whether histone modification marks are primary or secondary to transcription and whether they interact to form a histone code. We investigated the relationship between transcription and four histone modifications (H4ac, H3ac, H3K4me2/3) using ChIP-chip and expression microarray readouts from two murine cell lines, one in two differentiation stages. We found that their association with transcript levels strongly depends on the combination of histone modifications. H3K4me2 coincides with elevated expression levels only in combination with acetylation, while H3ac positive association is diminished by co-occurring modifications. During differentiation, upregulated transcripts frequently gain H4ac, while most modification conversions are uncorrelated with expression changes. Our results suggest histone modifications form a code, as their combinatorial composition is associated with distinct readouts. Histones may primarily function as signaling marks for specific effectors rather than being a sufficient driving force for or a consequence of transcription.
核小体参与DNA压缩和转录调控。然而,尚不清楚组蛋白修饰标记是转录的主要因素还是次要因素,以及它们是否相互作用形成组蛋白密码。我们使用来自两种小鼠细胞系(其中一种处于两个分化阶段)的ChIP芯片和表达微阵列读数,研究了转录与四种组蛋白修饰(H4ac、H3ac、H3K4me2/3)之间的关系。我们发现,它们与转录水平的关联很大程度上取决于组蛋白修饰的组合。仅在与乙酰化结合时,H3K4me2才与升高的表达水平一致,而同时发生的修饰会减弱H3ac的正相关。在分化过程中,上调的转录本经常获得H4ac,而大多数修饰转换与表达变化无关。我们的结果表明组蛋白修饰形成了一种密码,因为它们的组合组成与不同的读数相关。组蛋白可能主要作为特定效应器的信号标记,而不是转录的充分驱动力或结果。