Panetta G, Buttinelli M, Flaus A, Richmond T J, Rhodes D
MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, England.
J Mol Biol. 1998 Sep 25;282(3):683-97. doi: 10.1006/jmbi.1998.2087.
In Xenopus somatic cells histone H1 effects the transcriptional repression of oocyte type 5 S RNA genes, without altering the transcription of the somatic type 5 S RNA genes. Using an unambiguous nucleosome mapping method we find substantial differences between the multiple in vitro nucleosome positions on the two types of genes. These nucleosome positions determine both transcription factor and H1 binding, allowing TFIIIA to bind more efficiently to nucleosomes containing the somatic 5 S RNA gene than to nucleosomes on the oocyte 5 S RNA gene. Significantly, in a binding competition between TFIIIA and H1, TFIIIA preferentially binds to the somatic nucleosome whereas H1 preferentially binds to the oocyte nucleosome, excluding TFIIIA binding. These results strongly suggest that nucleosome positioning plays a key role in the regulation of transcription of 5 S RNA genes and provide a molecular mechanism for the selective repression of the oocyte 5 S RNA genes by H1.
在非洲爪蟾体细胞中,组蛋白H1可抑制卵母细胞5S RNA基因的转录,而不改变体细胞型5S RNA基因的转录。使用一种明确的核小体定位方法,我们发现这两种类型基因上多个体外核小体位置存在显著差异。这些核小体位置决定了转录因子和H1的结合,使得TFIIIA与含有体细胞5S RNA基因的核小体结合比与卵母细胞5S RNA基因上的核小体结合更有效。值得注意的是,在TFIIIA和H1的结合竞争中,TFIIIA优先结合体细胞核小体,而H1优先结合卵母细胞核小体,从而排除了TFIIIA的结合。这些结果强烈表明,核小体定位在5S RNA基因转录调控中起关键作用,并为H1对卵母细胞5S RNA基因的选择性抑制提供了分子机制。